Micro RNA expression constructs and uses thereof
11649455 · 2023-05-16
Assignee
- University Of Geneva (Geneva, N/A)
- LES HÔPITAUX UNIVERSITAIRES DE GENÈVE (Geneva, CH)
- University Of Zurich (Zurich, CH)
Inventors
- Karl-Heinz Krause (Geneva, CH)
- Francis Rousset (Geneva, CH)
- Patrick Salmon (Geneva, CH)
- Marco Alessandrini (Geneva, CH)
- Roberto Speck (Zurich, CH)
- Simon Bredl (Zurich, CH)
- Tafadzwa Mlambo (Zurich, CH)
- Renier Myburgh (Zurich, CH)
Cpc classification
C12N2320/32
CHEMISTRY; METALLURGY
C12N2310/51
CHEMISTRY; METALLURGY
C12N15/113
CHEMISTRY; METALLURGY
C12N15/1138
CHEMISTRY; METALLURGY
C12N15/86
CHEMISTRY; METALLURGY
International classification
C12N15/113
CHEMISTRY; METALLURGY
Abstract
The present disclosure relates to miRNA expression constructs, such as for expression of multiple miRNAs and use thereof to knockdown target gene expression. In some aspects, the expression constructs include a promoter element, a spacer sequence and a miRNA coding sequence. In some aspects, constructs provide enhanced immune cell function.
Claims
1. A miRNA expression construct comprising, from 5′ to 3′, a promoter element, a spacer between 300 and 600 nucleotides in length, and at least one miRNA hairpin, wherein the spacer is at least 80% identical to SEQ ID NO: 48 or SEQ ID NO: 49.
2. The miRNA expression construct of claim 1, wherein the promoter is a eukaryotic Pol II or Pol III promoter.
3. The miRNA expression construct of claim 2, wherein the promoter has a sequence at least 80% identical to SEQ ID NO: 45.
4. The miRNA expression construct of claim 1, wherein the miRNA hairpin comprises from 5′ to 3′ and in the order from (a)-(g): (a) a mir-16 flanking sequence comprising the sequence of SEQ ID NO: 25; (b) a first lower stem sequence comprising the mir-16 sequence of SEQ ID NO: 26, SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29 or SEQ ID NO: 30; (c) an anti-sense target sequence 22 nucleotides in length; (d) a mir-30 loop sequence comprising the sequence of SEQ ID NO: 31; (e) a sense sequence wherein the sequence is complementary to the sequence of (c) except that the sequence comprises one or two mismatches relative to the sequence of (c), wherein the one or two mismatches comprise: i) a mismatch located at the position 8 to 14 of the sense sequence, optionally located at position 11 of the sense sequence; and/or ii) a mismatch at the final 3′ position (position 22) of the sense sequence; (f) a second lower stem sequence wherein the sequence is complementary to the sequence of (b); and (g) a second flanking sequence, optionally wherein the flanking sequence is not complementary to the mir-16 flanking sequence of (a).
5. The miRNA expression construct of claim 1, wherein the nucleic acid molecule is DNA.
6. The miRNA expression construct of claim 1, comprising at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 miRNA hairpins.
7. The miRNA expression construct of claim 6, wherein at least two of the miRNA hairpins target the same sequence.
8. The miRNA expression construct of claim 6, wherein at least two of the miRNA hairpins target different sequences.
9. The miRNA expression construct of claim 1, wherein the miRNA expression construct further comprises a coding sequence for a heterologous protein.
10. The miRNA expression construct of claim 9, wherein the heterologous protein is a chimeric antigen receptor or a T cell receptor.
11. The miRNA expression construct of claim 1, wherein the miRNA expression construct further comprises a selection gene and/or a suicide gene.
12. The miRNA expression construct of claim 1, wherein the miRNA expression construct further comprises a peptide cleavage site.
13. An expression vector comprising the miRNA expression construct of claim 1.
14. A mammalian cell comprising the miRNA expression construct of claim 1.
15. The mammalian cell of claim 14, wherein the mammalian cell is an immune effector cell.
16. A method for preparing engineered immune effector cells, the method comprising transfecting or transducing the immune effector cells with the miRNA expression construct of claim 1.
17. The method of claim 16, comprising transducing or transfecting the immune effector cells with a chimeric antigen receptor or T cell receptor.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present invention. The invention may be better understood by reference to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.
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DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
I. The Present Embodiments
(21) The present invention relates generally to miRNA expression constructs. The present invention relates to constructs for the expression of multiple miRNAs. The present invention further relates to the use of a spacer sequence between the promoter and the miRNA sequences. In some aspects, the spacer sequence may be from GFP.
II. RNA Inhibition
(22) An inhibitory nucleic acid may inhibit the transcription of a gene or prevent the translation of a gene transcript in a cell. An inhibitory nucleic acid may be from 16 to 1000 nucleotides long, and in certain embodiments from 18 to 100 nucleotides long. In certain embodiments, the inhibitory nucleic acid is an isolated nucleic acid that binds or hybridizes to a gene of interest.
(23) Inhibitory nucleic acids are well known in the art. For example, siRNA, shRNA and double-stranded RNA have been described in U.S. Pat. Nos. 6,506,559 and 6,573,099, as well as in U.S. Patent Publications 2003/0051263, 2003/0055020, 2004/0265839, 2002/0168707, 2003/0159161, and 2004/0064842, all of which are herein incorporated by reference in their entirety.
(24) Since the discovery of RNAi by Fire and colleagues in 1998, the biochemical mechanisms have been rapidly characterized. Double stranded RNA (dsRNA) is cleaved by Dicer, which is an RNAase III family ribonuclease. This process yields miRNAs of ˜21 nucleotides in length. These miRNAs are incorporated into a multiprotein RNA-induced silencing complex (RISC) that is guided to target mRNA. RISC cleaves the target mRNA in the middle of the complementary region. In mammalian cells, the related miRNAs are found that are short RNA fragments (˜22 nucleotides). miRNAs are generated after Dicer-mediated cleavage of longer (˜70 nucleotide) precursors with imperfect hairpin RNA structures. The miRNA is incorporated into a miRNA-protein complex (miRNP), which leads to translational repression of target mRNA.
(25) In designing RNAi there are several factors that need to be considered such as the nature of the siRNA, the durability of the silencing effect, and the choice of delivery system. To produce an RNAi effect, the miRNA that is introduced into the organism will typically contain exonic sequences. Furthermore, the RNAi process is homology dependent, so the sequences must be carefully selected so as to maximize gene specificity, while minimizing the possibility of cross-interference between homologous, but not gene-specific sequences. Particularly the miRNA exhibits greater than 80, 85, 90, 95, 98% or even 100% identity between the sequence of the miRNA and a portion of the nucleotide sequence of a target gene. Sequences less than about 80% identical to the target gene are substantially less effective. Thus, the greater identity between the miRNA and the target gene to be inhibited, the less likely expression of unrelated genes will be affected.
(26) In addition, the size of the miRNA is an important consideration. In some embodiments, the present invention relates to miRNA molecules that include at least about 19-25 nucleotides, and are able to modulate target gene expression. In the context of the present invention, the miRNA is particularly less than 500, 200, 100, 50, 25, 24, 23 or 22 nucleotides in length. In some embodiments, the miRNA is from about 25 nucleotides to about 35 nucleotides or from about 19 nucleotides to about 25 nucleotides in length.
(27) To improve the effectiveness of miRNA-mediated gene silencing, guidelines for selection of target sites on mRNA have been developed for optimal design of miRNA (Soutschek et al., 2004; Wadhwa et al., 2004). These strategies may allow for rational approaches for selecting siRNA sequences to achieve maximal gene knockdown. To facilitate the entry of miRNA into cells and tissues, a variety of vectors including plasmids and viral vectors such as adenovirus, lentivirus, and retrovirus have been used (Wadhwa et al., 2004).
(28) Within an inhibitory nucleic acid, the components of a nucleic acid need not be of the same type or homogenous throughout (e.g., an inhibitory nucleic acid may comprise a nucleotide and a nucleic acid or nucleotide analog). Typically, an inhibitory nucleic acid form a double-stranded structure; the double-stranded structure may result from two separate nucleic acids that are partially or completely complementary. In certain embodiments of the present invention, the inhibitory nucleic acid may comprise only a single nucleic acid (polynucleotide) or nucleic acid analog and form a double-stranded structure by complementing with itself (e.g., forming a hairpin loop). The double-stranded structure of the inhibitory nucleic acid may comprise 16-500 or more contiguous nucleobases, including all ranges therebetween. The inhibitory nucleic acid may comprise 17 to 35 contiguous nucleobases, more particularly 18 to 30 contiguous nucleobases, more particularly 19 to 25 nucleobases, more particularly 20 to 23 contiguous nucleobases, or 20 to 22 contiguous nucleobases, or 21 contiguous nucleobases that hybridize with a complementary nucleic acid (which may be another part of the same nucleic acid or a separate complementary nucleic acid) to form a double-stranded structure.
(29) miRNA can be obtained from commercial sources, natural sources, or can be synthesized using any of a number of techniques well-known to those of ordinary skill in the art. For example, commercial sources of predesigned miRNA include Invitrogen's Stealth™ Select technology (Carlsbad, Calif.), Ambion® (Austin, Tex.), and Qiagen® (Valencia, Calif.). An inhibitory nucleic acid that can be applied in the compositions and methods of the present invention may be any nucleic acid sequence that has been found by any source to be a validated downregulator of a target gene.
(30) In some embodiments, the miRNA molecule is at least 75, 80, 85, or 90% homologous, particularly at least 95%, 99%, or 100% similar or identical, or any percentages in between the foregoing (e.g., the invention contemplates 75% and greater, 80% and greater, 85% and greater, and so on, and said ranges are intended to include all whole numbers in between), to at least 10 contiguous nucleotides of any of the nucleic acid sequences encoding a full-length protein.
(31) The miRNA may also comprise an alteration of one or more nucleotides. Such alterations can include the addition of non-nucleotide material, such as to the end(s) of the 19 to 25 nucleotide RNA or internally (at one or more nucleotides of the RNA). In certain aspects, the RNA molecule contains a 3′-hydroxyl group. Nucleotides in the RNA molecules of the present invention can also comprise non-standard nucleotides, including non-naturally occurring nucleotides or deoxyribonucleotides. The double-stranded oligonucleotide may contain a modified backbone, for example, phosphorothioate, phosphorodithioate, or other modified backbones known in the art, or may contain non-natural internucleoside linkages. Additional modifications of siRNAs (e.g., 2′-O-methyl ribonucleotides, 2′-deoxy-2′-fluoro ribonucleotides, “universal base” nucleotides, 5-C-methyl nucleotides, one or more phosphorothioate internucleotide linkages, and inverted deoxyabasic residue incorporation) can be found in U.S. Publication 2004/0019001 and U.S. Pat. No. 6,673,611 (each of which is incorporated by reference in its entirety). Collectively, all such altered nucleic acids or RNAs described above are referred to as modified miRNAs.
II. Vectors for Cloning, Gene Transfer and Expression
(32) Within certain aspects expression vectors are employed to express a nucleic acid of interest, such as a nucleic acid that inhibits the expression of a particular gene. Expression requires that appropriate signals be provided in the vectors, and which include various regulatory elements, such as enhancers/promoters from both viral and mammalian sources that drive expression of the genes of interest in host cells. Elements designed to optimize RNA stability in host cells also are defined. The conditions for the use of a number of dominant drug selection markers for establishing permanent, stable cell clones expressing the products are also provided, as is an element that links expression of the drug selection markers to expression of the polypeptide.
(33) A. Regulatory Elements
(34) Throughout this application, the term “expression construct” or “expression vector” is meant to include any type of genetic construct containing a nucleic acid coding for a gene product in which part or all of the nucleic acid encoding sequence is capable of being transcribed. The transcript may be translated into a protein, but it need not be. In certain embodiments, expression includes both transcription of a gene and translation of mRNA into a gene product. In other embodiments, expression only includes transcription of the nucleic acid encoding a gene of interest i.e., as is the case with RNA molecules of the embodiments.
(35) In certain embodiments, the nucleic acid encoding a gene product is under transcriptional control of a promoter. A “promoter” refers to a DNA sequence recognized by the synthetic machinery of the cell, or introduced synthetic machinery, required to initiate the specific transcription of a gene. The phrase “under transcriptional control” means that the promoter is in the correct location and orientation in relation to the nucleic acid to control RNA polymerase initiation and expression of the gene.
(36) The term promoter will be used here to refer to a group of transcriptional control modules that are clustered around the initiation site for eukaryotic RNA polymerase (Pol) I, II or III. Much of the thinking about how promoters are organized derives from analyses of several viral Pol II promoters, including those for the HSV thymidine kinase (tk) and SV40 early transcription units. These studies, augmented by more recent work, have shown that promoters are composed of discrete functional modules, each consisting of approximately 7-20 bp of DNA, and containing one or more recognition sites for transcriptional activator or repressor proteins.
(37) At least one module in each promoter functions to position the start site for RNA synthesis. The best known example of this is the TATA box, but in some promoters lacking a TATA box, such as the promoter for the mammalian terminal deoxynucleotidyl transferase gene and the promoter for the SV40 late genes, a discrete element overlying the start site itself helps to fix the place of initiation.
(38) Additional promoter elements regulate the frequency of transcriptional initiation. Typically, these are located in the region 30-110 bp upstream of the start site, although a number of promoters have recently been shown to contain functional elements downstream of the start site as well. The spacing between promoter elements frequently is flexible, so that promoter function is preserved when elements are inverted or moved relative to one another. In the tk promoter, the spacing between promoter elements can be increased to 50 bp apart before activity begins to decline. Depending on the promoter, it appears that individual elements can function either co-operatively or independently to activate transcription.
(39) In some embodiments, the promoter comprises an Elongation Factor 1 short (EF1s) promoter. In other embodiments, the human cytomegalovirus (CMV) immediate early gene promoter, the SV40 early promoter, the Rous sarcoma virus long terminal repeat, rat insulin promoter and glyceraldehyde-3-phosphate dehydrogenase can be used to obtain high-level expression of the coding sequence of interest. The use of other viral or mammalian cellular or bacterial phage promoters which are well-known in the art to achieve expression of a coding sequence of interest is contemplated as well, provided that the levels of expression are sufficient for a given purpose.
(40) By employing a promoter with well-known properties, the level and pattern of expression of the protein of interest following transfection or transformation can be optimized. Further, selection of a promoter that is regulated in response to specific physiologic signals can permit inducible expression of the gene product. Tables 1 and 2 list several regulatory elements that may be employed, in the context of the present invention, to regulate the expression of the gene of interest. This list is not intended to be exhaustive of all the possible elements involved in the promotion of gene expression but, merely, to be exemplary thereof. In some aspects, a promoter for use according to the instant embodiments is a non-tissue specific promoter, such as a constitutive promoter.
(41) Enhancers are genetic elements that increase transcription from a promoter located at a distant position on the same molecule of DNA. Enhancers are organized much like promoters. That is, they are composed of many individual elements, each of which binds to one or more transcriptional proteins.
(42) The basic distinction between enhancers and promoters is operational. An enhancer region as a whole must be able to stimulate transcription at a distance; this need not be true of a promoter region or its component elements. On the other hand, a promoter must have one or more elements that direct initiation of RNA synthesis at a particular site and in a particular orientation, whereas enhancers lack these specificities. Promoters and enhancers are often overlapping and contiguous, often seeming to have a very similar modular organization.
(43) Below is a list of viral promoters, cellular promoters/enhancers and inducible promoters/enhancers that could be used in combination with the nucleic acid encoding a gene or miRNA of interest in an expression construct (Table 1 and Table 2). Additionally, any promoter/enhancer combination (as per the Eukaryotic Promoter Data Base EPDB) could also be used to drive expression of the gene or miRNA of interest. Truncated promoters may also be used to drive expression. Eukaryotic cells can support cytoplasmic transcription from certain bacterial promoters if the appropriate bacterial polymerase is provided, either as part of the delivery complex or as an additional genetic expression construct.
(44) TABLE-US-00001 TABLE 1 Promoter and/or Enhancer Promoter/Enhancer References Elongation Factor 1 alpha (EF1α) Kim et al., 1990 Immunoglobulin Heavy Chain Banerji et al., 1983; Gilles et al., 1983; Grosschedl et al., 1985; Atchinson et al., 1986, 1987; Imler et al., 1987; Weinberger et al., 1984; Kiledjian et al., 1988; Porton et al.; 1990 Immunoglobulin Light Chain Queen et al., 1983; Picard et al., 1984 T-Cell Receptor Luria et al., 1987; Winoto et al., 1989; Redondo et al.; 1990 HLA DQ a and/or DQ β Sullivan et al., 1987 β-Interferon Goodbourn et al., 1986; Fujita et al., 1987; Goodbourn et al., 1988 Interleukin-2 Greene et al., 1989 Interleukin-2 Receptor Greene et al., 1989; Lin et al., 1990 MHC Class II 5 Koch et al., 1989 MHC Class II HLA-DRa Sherman et al., 1989 β-Actin Kawamoto et al., 1988; Ng et al.; 1989 Muscle Creatine Kinase (MCK) Jaynes et al., 1988; Horlick et al., 1989; Johnson et al., 1989 Prealbumin (Transthyretin) Costa et al., 1988 Elastase I Ornitz et al., 1987 Metallothionein (MTII) Karin et al., 1987; Culotta et al., 1989 Collagenase Pinkert et al., 1987; Angel et al., 1987a Albumin Pinkert et al., 1987; Tronche et al., 1989, 1990 α-Fetoprotein Godbout et al., 1988; Campere et al., 1989 t-Globin Bodine et al., 1987; Perez-Stable et al., 1990 β-Globin Trudel et al., 1987 c-fos Cohen et al., 1987 c-HA-ras Triesman, 1986; Deschamps et al., 1985 Insulin Edlund et al., 1985 Neural Cell Adhesion Molecule Hirsh et al., 1990 (NCAM) α.sub.1-Antitrypain Latimer et al., 1990 H2B (TH2B) Histone Hwang et al., 1990 Mouse and/or Type I Collagen Ripe et al., 1989 Glucose-Regulated Proteins Chang et al., 1989 (GRP94 and GRP78) Rat Growth Hormone Larsen et al., 1986 Human Serum Amyloid A (SAA) Edbrooke et al., 1989 Troponin I (TN I) Yutzey et al., 1989 Platelet-Derived Growth Pech et al., 1989 Factor (PDGF) Duchenne Muscular Dystrophy Klamut et al., 1990 SV40 Banerji et al., 1981; Moreau et al., 1981; Sleigh et al., 1985; Firak et al., 1986; Herr et al., 1986; Imbra et al., 1986; Kadesch et al., 1986; Wang et al., 1986; Ondek et al., 1987; Kuhl et al., 1987; Schaffner et al., 1988 Polyoma Swartzendruber et al., 1975; Vasseur et al., 1980; Katinka et al., 1980, 1981; Tyndell et al., 1981; Dandolo et al., 1983; de Villiers et al., 1984; Hen et al., 1986; Satake et al., 1988; Campbell and/or Villarreal, 1988 Retroviruses Kriegler et al., 1982, 1983; Levinson et al., 1982; Kriegler et al., 1983, 1984a, b, 1988; Bosze et al., 1986; Miksicek et al., 1986; Celander et al., 1987; Thiesen et al., 1988; Celander et al., 1988; Choi et al., 1988; Reisman et al., 1989 Papilloma Virus Campo et al., 1983; Lusky et al., 1983; Spandidos and/or Wilkie, 1983; Spalholz et al., 1985; Lusky et al., 1986; Cripe et al., 1987; Gloss et al., 1987; Hirochika et al., 1987; Stephens et al., 1987 Hepatitis B Virus Bulla et al., 1986; Jameel et al., 1986; Shaul et al., 1987; Spandau et al., 1988; Vannice et al., 1988 Human Immunodeficiency Muesing et al., 1987; Hauber et al., 1988; Virus Jakobovits et al., 1988; Feng et al., 1988; Takebe et al., 1988; Rosen et al., 1988; Berkhout et al., 1989; Laspia et al., 1989; Sharp et al., 1989; Braddock et al., 1989 Cytomegalovirus (CMV) Weber et al., 1984; Boshart et al., 1985; Foecking et al., 1986 Gibbon Ape Leukemia Virus Holbrook et al., 1987; Quinn et al., 1989
(45) TABLE-US-00002 TABLE 2 Inducible Elements Element Inducer References MT II Phorbol Ester (TFA) Palmiter et al., 1982; Heavy metals Haslinger et al., 1985; Searle et al., 1985; Stuart et al., 1985; Imagawa et al., 1987, Karin et al., 1987; Angel et al., 1987b; McNeall et al., 1989 MMTV (mouse Glucocorticoids Huang et al., 1981; Lee et mammary al., 1981; Majors et al., tumor virus) 1983; Chandler et al., 1983; Ponta et al., 1985; Sakai et aL , 1988 β-Interferon poly(rI)x Tavernier et al., 1983 poly(rc) Adenovirus 5 E2 ElA Imperiale et al., 1984 Collagenase Phorbol Ester (TPA) Angel et al., 1987a Stromelysin Phorbol Ester (TPA) Angel et al., 1987b SV40 Phorbol Ester (TPA) Angel et al., 1987b Murine MX Gene Interferon, Newcastle Hug et al., 1988 Disease Virus GRP78 Gene A23187 Resendez et al., 1988 α-2-Macroglobulin IL-6 Kunz et al., 1989 Vimentin Serum Rittling et al., 1989 MHC Class I Interferon Blanar et al., 1989 Gene H-2κb HSP70 ElA, SV40 Large Taylor et al., 1989, 1990a, T Antigen 1990b Proliferin Phorbol Ester-TPA Mordacq et al., 1989 Tumor Necrosis Factor PMA Hensel et al., 1989 Thyroid Stimulating Thyroid Hormone Chatterjee et al., 1989 Hormone α Gene
(46) Where any cDNA insert is employed, one will typically include a polyadenylation signal to effect proper polyadenylation of the gene transcript. The nature of the polyadenylation signal is not believed to be crucial to the successful practice of the invention, and any such sequence may be employed such as human growth hormone and SV40 polyadenylation signals. In some aspects, however, a polyadenylation signal sequence is not included in a vector of the embodiments. For example, incorporation of such a signal sequence in lentiviral vectors (before a 3′ LTR) can reduce resulting lentiviral titers.
(47) A spacer sequence may be included in the nucleic acid construct. The presence of a spacer appears to enhance knockdown efficiency of miRNA (Stegmeier et al., 2005). Spacers may be any nucleotide sequence. In some aspects, the spacer is GFP.
(48) Also contemplated as an element of the expression cassette is a terminator. These elements can serve to enhance message levels and to minimize read through from the cassette into other sequences.
(49) B. Selectable Markers
(50) In certain embodiments of the invention, the cells contain nucleic acid constructs of the present invention, a cell may be identified in vitro, ex vivo or in vivo by including a marker in the expression construct. Such markers would confer an identifiable change to the cell permitting easy identification of cells containing the expression construct. Usually the inclusion of a drug selection marker aids in cloning and in the selection of transformants, for example, genes that confer resistance to neomycin, puromycin, hygromycin, DHFR, GPT, zeocin and histidinol are useful selectable markers. Alternatively, enzymes such as herpes simplex virus thymidine kinase (tk) or chloramphenicol acetyltransferase (CAT) may be employed. Immunologic markers also can be employed. The selectable marker employed is not believed to be important, so long as it is capable of being expressed simultaneously with the nucleic acid encoding a gene product. Further examples of selectable markers are well known to one of skill in the art.
III. Delivery of Nucleic Acid Molecules and Expression Vectors
(51) In certain aspects, vectors for delivery of nucleic acids of the embodiments could be constructed to express these factors in cells. In a particular aspect, the following systems and methods may be used in delivery of nucleic acids to desired cell types.
(52) A. Homologous Recombination
(53) In certain aspects of the embodiments, the vectors encoding nucleic acid molecules of the embodiments may be introduced into cells in a specific manner, for example, via homologous recombination. Current approaches to express genes in stem cells have involved the use of viral vectors (e.g., lentiviral vectors) or transgenes that integrate randomly in the genome. These approaches have not been successful due in part because the randomly integrated vectors can activate or suppress endogenous gene expression, and/or the silencing of transgene expression. The problems associated with random integration could be partially overcome by homologous recombination to a specific locus in the target genome.
(54) Homologous recombination (HR), also known as general recombination, is a type of genetic recombination used in all forms of life in which nucleotide sequences are exchanged between two similar or identical strands of DNA. The technique has been the standard method for genome engineering in mammalian cells since the mid 1980s. The process involves several steps of physical breaking and the eventual rejoining of DNA. This process is most widely used in nature to repair potentially lethal double-strand breaks in DNA. In addition, homologous recombination produces new combinations of DNA sequences during meiosis, the process by which eukaryotes make germ cells like sperm and ova. These new combinations of DNA represent genetic variation in offspring which allow populations to evolutionarily adapt to changing environmental conditions over time. Homologous recombination is also used in horizontal gene transfer to exchange genetic material between different strains and species of bacteria and viruses. Homologous recombination is also used as a technique in molecular biology for introducing genetic changes into target organisms.
(55) Homologous recombination can be used as targeted genome modification. The efficiency of standard HR in mammalian cells is only 10.sup.−6 to 10.sup.−9 of cells treated (Capecchi, 1990). The use of meganucleases, or homing endonucleases, such as I-SceI have been used to increase the efficiency of HR. Both natural meganucleases as well as engineered meganucleases with modified targeting specificities have been utilized to increase HR efficiency (Pingoud and Silva, 2007; Chevalier et al., 2002). Another path toward increasing the efficiency of HR has been to engineer chimeric endonucleases with programmable DNA specificity domains (Silva et al., 2011). Zinc-finger nucleases (ZFN) are one example of such a chimeric molecule in which Zinc-finger DNA binding domains are fused with the catalytic domain of a Type IIS restriction endonuclease such as FokI (as reviewed in Durai et al., 2005; PCT/US2004/030606). Another class of such specificity molecules includes Transcription Activator Like Effector (TALE) DNA binding domains fused to the catalytic domain of a Type IIS restriction endonuclease such as FokI (Miller et al., 2011: PCT/IB2010/000154).
(56) B. Nucleic Acid Delivery Systems
(57) One of skill in the art would be well equipped to construct a vector through standard recombinant techniques (see, for example, Sambrook et al., 2001 and Ausubel et al., 1996, both incorporated herein by reference). Vectors include but are not limited to, plasmids, cosmids, viruses (bacteriophage, animal viruses, and plant viruses), and artificial chromosomes (e.g., YACs), such as retroviral vectors (e.g., derived from Moloney murine leukemia virus vectors (MoMLV), MSCV, SFFV, MPSV, SNV etc), lentiviral vectors (e.g., derived from HIV-1, HIV-2, SIV, BIV, FIV etc.), adenoviral (Ad) vectors including replication competent, replication deficient and gutless forms thereof, adeno-associated viral (AAV) vectors, simian virus 40 (SV-40) vectors, bovine papilloma virus vectors, Epstein-Barr virus, herpes virus vectors, vaccinia virus vectors, Harvey murine sarcoma virus vectors, murine mammary tumor virus vectors, Rous sarcoma virus vectors.
(58) 1. Episomal Vectors
(59) The use of plasmid- or liposome-based extra-chromosomal (i.e., episomal) vectors may be also provided in certain aspects of the invention, for example, for reprogramming of somatic cells. Such episomal vectors may include, e.g., oriP-based vectors, and/or vectors encoding a derivative of EBV-protein EBNA-1. These vectors may permit large fragments of DNA to be introduced to a cell and maintained extra-chromosomally, replicated once per cell cycle, partitioned to daughter cells efficiently, and elicit substantially no immune response.
(60) In particular, EBNA-1, the only viral protein required for the replication of the oriP-based expression vector, does not elicit a cellular immune response because it has developed an efficient mechanism to bypass the processing required for presentation of its antigens on MHC class I molecules (Levitskaya et al., 1997). Further, EBNA-1 can act in trans to enhance expression of the cloned gene, inducing expression of a cloned gene up to 100-fold in some cell lines (Langle-Rouault et al., 1998; Evans et al., 1997). Finally, the manufacture of such oriP-based expression vectors is inexpensive.
(61) Other extra-chromosomal vectors include other lymphotrophic herpes virus-based vectors. Lymphotrophic herpes virus is a herpes virus that replicates in a lymphoblast (e.g., a human B lymphoblast) and becomes a plasmid for a part of its natural life-cycle. Herpes simplex virus (HSV) is not a “lymphotrophic” herpes virus. Exemplary lymphotrophic herpes viruses include, but are not limited to EBV, Kaposi's sarcoma herpes virus (KSHV); Herpes virus saimiri (HS) and Marek's disease virus (MDV). Also other sources of episome-based vectors are contemplated, such as yeast ARS, adenovirus, SV40, or BPV.
(62) One of skill in the art would be well equipped to construct a vector through standard recombinant techniques (see, for example, Maniatis et al., 1988 and Ausubel et al., 1994, both incorporated herein by reference).
(63) Vectors can also comprise other components or functionalities that further modulate gene delivery and/or gene expression, or that otherwise provide beneficial properties to the targeted cells. Such other components include, for example, components that influence binding or targeting to cells (including components that mediate cell-type or tissue-specific binding); components that influence uptake of the vector nucleic acid by the cell; components that influence localization of the polynucleotide within the cell after uptake (such as agents mediating nuclear localization); and components that influence expression of the polynucleotide.
(64) Such components also might include markers, such as detectable and/or selection markers that can be used to detect or select for cells that have taken up and are expressing the nucleic acid delivered by the vector. Such components can be provided as a natural feature of the vector (such as the use of certain viral vectors which have components or functionalities mediating binding and uptake), or vectors can be modified to provide such functionalities. A large variety of such vectors are known in the art and are generally available. When a vector is maintained in a host cell, the vector can either be stably replicated by the cells during mitosis as an autonomous structure, incorporated within the genome of the host cell, or maintained in the host cell's nucleus or cytoplasm.
(65) 2. Transposon-Based System
(66) According to a particular embodiment the introduction of nucleic acids may use a transposon-transposase system. The used transposon-transposase system could be the well known Sleeping Beauty, the Frog Prince transposon-transposase system (for the description of the latter see e.g., EP1507865), or the TTAA-specific transposon piggyback system.
(67) Transposons are sequences of DNA that can move around to different positions within the genome of a single cell, a process called transposition. In the process, they can cause mutations and change the amount of DNA in the genome. Transposons were also once called jumping genes, and are examples of mobile genetic elements.
(68) There are a variety of mobile genetic elements, and they can be grouped based on their mechanism of transposition. Class I mobile genetic elements, or retrotransposons, copy themselves by first being transcribed to RNA, then reverse transcribed back to DNA by reverse transcriptase, and then being inserted at another position in the genome. Class II mobile genetic elements move directly from one position to another using a transposase to “cut and paste” them within the genome.
(69) 3. Viral Vectors
(70) In generating recombinant viral vectors, non-essential genes are typically replaced with a gene or coding sequence for a heterologous (or non-native) protein or nucleic acid. Viral vectors are a kind of expression construct that utilizes viral sequences to introduce nucleic acid and possibly proteins into a cell. The ability of certain viruses to infect cells or enter cells via pH-dependent or pH-independent mechanisms, to integrate their genetic cargo into a host cell genome and to express viral genes stably and efficiently have made them attractive candidates for the transfer of foreign nucleic acids into cells (e.g., mammalian cells). Non-limiting examples of virus vectors that may be used to deliver a nucleic acid of certain aspects of the present invention are described below.
(71) Retroviruses have promise as gene delivery vectors due to their ability to integrate their genes into the host genome, transferring a large amount of foreign genetic material, infecting a broad spectrum of species and cell types and of being packaged in special cell-lines (Miller, 1992).
(72) In order to construct a retroviral vector, a nucleic acid is inserted into the viral genome in the place of certain viral sequences to produce a virus that is replication-defective. In order to produce virions, a packaging cell line containing the gag, pol, and env genes but without the LTR and packaging components is constructed (Mann et al., 1983). When a recombinant plasmid containing a cDNA, together with the retroviral LTR and packaging sequences is introduced into a special cell line (e.g., by calcium phosphate precipitation for example), the packaging sequence allows the RNA transcript of the recombinant plasmid (i.e., the vector genome) to be packaged into viral particles, which are then secreted into the culture media (Nicolas and Rubenstein, 1988; Temin, 1986; Mann et al., 1983). The media containing the recombinant retroviruses is then collected, optionally concentrated, and used for gene transfer. Depending on the tropism of the envelope protein used to cover the vector particles surface, retroviral vectors are able to infect a broad variety of cell types. However, integration and stable expression require the division of host cells (Paskind et al., 1975).
(73) Lentiviruses are complex retroviruses, which, in addition to the common retroviral genes gag, pol, and env, contain other genes with regulatory or structural function. Lentiviral vectors are well known in the art (see, for example, Naldini et al., 1996; Zufferey et al., 1997; Blomer et al., 1997; Giry-Laterriere et al., 2011; U.S. Pat. Nos. 6,013,516 and 5,994,136).
(74) Recombinant lentiviral vectors are capable of infecting non-dividing cells and can be used for both in vivo and ex vivo gene transfer and expression of nucleic acid sequences. For example, recombinant lentivirus capable of infecting a non-dividing cell wherein a suitable host cell is transfected with two or more vectors carrying the packaging functions, namely gag, pol and env, as well as rev and tat is described in U.S. Pat. No. 5,994,136, incorporated herein by reference.
(75) C. Nucleic Acid Delivery
(76) Introduction of a nucleic acid, such as DNA or RNA, into cells to be programmed with the current invention may use any suitable methods for nucleic acid delivery for transformation of a cell, as described herein or as would be known to one of ordinary skill in the art. Such methods include, but are not limited to, direct delivery of DNA such as by ex vivo transfection (Wilson et al., 1989, Nabel et al, 1989), by injection (U.S. Pat. Nos. 5,994,624, 5,981,274, 5,945,100, 5,780,448, 5,736,524, 5,702,932, 5,656,610, 5,589,466 and 5,580,859, each incorporated herein by reference), including microinjection (Harland and Weintraub, 1985; U.S. Pat. No. 5,789,215, incorporated herein by reference); by electroporation (U.S. Pat. No. 5,384,253, incorporated herein by reference; Tur-Kaspa et al., 1986; Potter et al., 1984); by calcium phosphate precipitation (Graham and Van Der Eb, 1973; Chen and Okayama, 1987; Rippe et al., 1990); by using DEAE-dextran followed by polyethylene glycol (Gopal, 1985); by direct sonic loading (Fechheimer et al., 1987); by liposome mediated transfection (Nicolau and Sene, 1982; Fraley et al., 1979; Nicolau et al., 1987; Wong et al., 1980; Kaneda et al., 1989; Kato et al., 1991) and receptor-mediated transfection (Wu and Wu, 1987; Wu and Wu, 1988); by microprojectile bombardment (PCT Application Nos. WO 94/09699 and 95/06128; U.S. Pat. Nos. 5,610,042; 5,322,783, 5,563,055, 5,550,318, 5,538,877 and 5,538,880, and each incorporated herein by reference); by agitation with silicon carbide fibers (Kaeppler et al., 1990; U.S. Pat. Nos. 5,302,523 and 5,464,765, each incorporated herein by reference); by Agrobacterium-mediated transformation (U.S. Pat. Nos. 5,591,616 and 5,563,055, each incorporated herein by reference); by desiccation/inhibition-mediated DNA uptake (Potrykus et al., 1985), and any combination of such methods. Through the application of techniques such as these, organelle(s), cell(s), tissue(s) or organism(s) may be stably or transiently transformed.
(77) 1. Liposome-Mediated Transfection
(78) In a certain embodiment of the invention, a nucleic acid may be entrapped in a lipid complex such as, for example, a liposome. Liposomes are vesicular structures characterized by a phospholipid bilayer membrane and an inner aqueous medium. Multilamellar liposomes have multiple lipid layers separated by aqueous medium. They form spontaneously when phospholipids are suspended in an excess of aqueous solution. The lipid components undergo self-rearrangement before the formation of closed structures and entrap water and dissolved solutes between the lipid bilayers (Ghosh and Bachhawat, 1991). Also contemplated is an nucleic acid complexed with Lipofectamine (Gibco BRL) or Superfect (Qiagen). The amount of liposomes used may vary upon the nature of the liposome as well as the cell used, for example, about 5 to about 20 μg vector DNA per 1 to 10 million of cells may be contemplated.
(79) Liposome-mediated nucleic acid delivery and expression of foreign DNA in vitro has been very successful (Nicolau and Sene, 1982; Fraley et al., 1979; Nicolau et al., 1987). The feasibility of liposome-mediated delivery and expression of foreign DNA in cultured chick embryo, HeLa and hepatoma cells has also been demonstrated (Wong et al., 1980).
(80) In certain embodiments of the invention, a liposome may be complexed with a hemagglutinating virus (HVJ). This has been shown to facilitate fusion with the cell membrane and promote cell entry of liposome-encapsulated DNA (Kaneda et al., 1989). In other embodiments, a liposome may be complexed or employed in conjunction with nuclear non-histone chromosomal proteins (HMG-1) (Kato et al., 1991). In yet further embodiments, a liposome may be complexed or employed in conjunction with both HVJ and HMG-1. In other embodiments, a delivery vehicle may comprise a ligand and a liposome.
(81) 2. Electroporation
(82) In certain embodiments of the present invention, a nucleic acid is introduced into an organelle, a cell, a tissue or an organism via electroporation. Electroporation involves the exposure of a suspension of cells and DNA to a high-voltage electric discharge. Recipient cells can be made more susceptible to transformation by mechanical wounding. Also the amount of vectors used may vary upon the nature of the cells used, for example, about 5 to about 20 g vector DNA per 1 to 10 million of cells may be contemplated.
(83) Transfection of eukaryotic cells using electroporation has been quite successful. Mouse pre-B lymphocytes have been transfected with human kappa-immunoglobulin genes (Potter et al., 1984), and rat hepatocytes have been transfected with the chloramphenicol acetyltransferase gene (Tur-Kaspa et al., 1986) in this manner.
(84) 3. Calcium Phosphate
(85) In other embodiments of the present invention, a nucleic acid is introduced to the cells using calcium phosphate precipitation. Human KB cells have been transfected with adenovirus 5 DNA (Graham and Van Der Eb, 1973) using this technique. Also in this manner, mouse L(A9), mouse C127, CHO, CV-1, BHK, NIH3T3 and HeLa cells were transfected with a neomycin marker gene (Chen and Okayama, 1987), and rat hepatocytes were transfected with a variety of marker genes (Rippe et al., 1990).
(86) 4. DEAE-Dextran
(87) In another embodiment, a nucleic acid is delivered into a cell using DEAE-dextran followed by polyethylene glycol. In this manner, reporter plasmids were introduced into mouse myeloma and erythroleukemia cells (Gopal, 1985).
(88) D. Cell Culturing
(89) Generally, cells of the present invention are cultured in a culture medium, which is a nutrient-rich buffered solution capable of sustaining cell growth.
(90) Culture media suitable for isolating, expanding and differentiating stem cells according to the method described herein include but not limited to high glucose Dulbecco's Modified Eagle's Medium (DMEM), DMEM/F-12, Liebovitz L-15, RPMI 1640, Iscove's modified Dubelcco's media (IMDM), and Opti-MEM SFM (Invitrogen Inc.). Chemically Defined Medium comprises a minimum essential medium such as Iscove's Modified Dulbecco's Medium (IMDM) (Gibco), supplemented with human serum albumin, human Ex Cyte lipoprotein, transferrin, insulin, vitamins, essential and non essential amino acids, sodium pyruvate, glutamine and a mitogen is also suitable. As used herein, a mitogen refers to an agent that stimulates cell division of a cell. An agent can be a chemical, usually some form of a protein that encourages a cell to commence cell division, triggering mitosis. In one embodiment, serum free media such as those described in U.S. Ser. No. 08/464,599 and WO96/39487, and the “complete media” as described in U.S. Pat. No. 5,486,359 are contemplated for use with the method described herein. In some embodiments, the culture medium is supplemented with 10% Fetal Bovine Serum (FBS), human autologous serum, human AB serum or platelet rich plasma supplemented with heparin (2U/ml). Cell cultures may be maintained in a CO.sub.2 atmosphere, e.g., 5% to 12%, to maintain pH of the culture fluid, incubated at 37° C. in a humid atmosphere and passaged to maintain a confluence below 85%.
IV. EXAMPLES
(91) The following examples are included to demonstrate preferred embodiments of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent techniques discovered by the inventor to function well in the practice of the invention, and thus can be considered to constitute preferred modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.
Example 1—Materials and Methods
(92) Construction of miRNA-containing plasmids and lentiviral vectors. The plasmids were constructed using the gateway system as described previously (Myburgh et al., 2014). With the exception of MGST2, spacer sequences were amplified by PCR using Herculase II polymerase (Agilent, Santa Clara, Calif.) with forward and reverse primers carrying respectively EcoRI and XhoI restriction sites and cloned into a pENTR vector (Invitrogen) by digestion/ligation steps (Table 3). Most of the primers used for the cloning of spacers were designed with AttB1 (forward primer) and AttB2 (reverse primer) recombination sites at the 5′ extremity (Table 4).
(93) The MGST2 spacer was obtained from pOTB7-MGST2 plasmid (transomic) by EcoRI/XhoI restriction digestion and subsequent ligation into the pENTR vector. mirGE hairpins were amplified using the same strategy and forward and reverse primers carrying respectively SpeI and BamHI restriction sites. Elements of the miRGE hairpins can be seen in Table 5. miRGE hairpin concatenates were made using different couples of restriction enzymes on the miRGE primers or by blunt ligation as in Sun et al, 2006. Each new miRGE addition was verified by sequencing the pENTR vector. The amplicon parts of each clone, including spacer and miRGE hairpins were systematically verified by sequencing. The oligos for the miRGE PCR template and primers were obtained from Microsynth (Balgach, Switzerland). miRGE hairpin template sequences targeting CCR5, GFP and p22.sup.phox are available in Table 6.
(94) The final lentivector plasmid was generated by an LR Clonase II (Invitrogen, Carlsbad, Calif.)-mediated recombination of a pENTR plasmid containing the human UBI promoter (pENTR-L4-UBI-L1R) or the Elongation Factor 1 short promoter (pENTR-L4-EFs-L1R) and a lentivector destination cassette (pCWX-R4dEST-R2-PC) containing an additional transcription unit encoding for mCherry marker gene upon human phosphoglycerate kinase 1 (PGK) promoter. The GFP target sequence-AAGAACGGCATCAAGGTGAACT (SEQ ID NO:57)—was taken from a previous publication (Mottet-Osman et al., 2007). The human CCR5 (Genbank NM_000579.3) target sequences (T7) 5′aAGTGTCAAGTCCAATCTATGA (SEQ ID NO:58) was previously used (Myburgh et al., 2014).
(95) TABLE-US-00003 TABLE 3 Lentivectors and titers. Lentivector Titer (TU/mL) pCWX-UBI-mcherry (control vector) 3.55E+06 pCWX-UBI-No spacer-mirGE CCR5-7-PGK-mCherry 1.02E+07 pCWX-UBI-GFP-mirGE CCR5-7-PGK-mCherry 4.66E+06 pCWX-UBI-mirGE CCR5-7-GFP-PGK-mCherry 1.17E+07 pCWX-UBI-MGST2-miRGE CCR5-7-PGK-mCherry 7.80E+05 pCWX-UBI-NGFR-miRGE CCR5-7-PGK-mCherry 1.94E+05 pCWX-UBI-CD4 R1-miRGE CCR5-7-PGK-mCherry 1.80E+06 pCWX-UBI-CD4 R2-miRGE CCR5-7-PGK-mCherry 2.76E+06 pCWX-UBI-CD4 R3-miRGE CCR5-7-PGK-mCherry 2.52E+06 pCWX-UBI-HO-1-miRGE CCR5-7-PGK-mCherry 1.60E+06 pCWX-UBI-H2B-miRGE CCR5-7-PGK-mCherry 1.22E+07 pCWX-UBI-stopGFP-miRGE CCR5-7-PGK-mCherry 3.54E+06 pCWX-UBI-GFPpart1-miRGE CCR5-7-PGK-mCherry 1.56E+06 pCWX-UBI-GFPpart2-miRGE CCR5-7-PGK-mCherry 1.59E+06 pCWX-UBI-MGST2-miRGE CYBA 222-PGK-mCherry 1.57E+06 pCWX-UBI-stopGFP-mirGE CYBA 222-PGK-mCherry 2.31E+06 pCWX-UBI- MGST2-mirGE-CCR5-777-PGK-mCherry 1.34E+07 pCWX-UBI- MGST2-mirGE-CCR5-777GFP-PGK-mCherry 1.20E+07 pCWX-UBI- MGST2-mirGE-CCR5-7777-PGK-mCherry 1.10E+05 pCWX-UBI- MGST2-mirGE-CCR5-7777GFP-PGK-mCherry 1.28E+07 pCWX-UBI-No spacer-mirGE CCR5-777-PGK-mCherry 6.81E+06 pCWX-UBI-mirGE CCR5-777-GFP-PGK-mCherry 1.10E+07 pCWX-UBI-H2B-miRGE CCR5-777-PGK-mCherry 5.06E+06 pCWX-UBI- stopGFP-mirGE-CCR5-777-PGK-mCherry 1.00E+06 pCWX-UBI- stopGFP-mirGE-CCR5-777GFP-PGK-mCherry 1.84E+05 pCWX-UBI- stopGFP-mirGE-CCR5-7777-PGK-mCherry 1.98E+06 pCWX-UBI- stopGFP-mirGE-CCR5-7777GFP-PGK-mCherry 1.12E+06 pCWX-UBI-stopGFP-miRGEGFP-PGK-mCherry 9.02E+05 pCWX-EFs-No spacer-mirGE CCR5-7-PGK-mCherry 9.25E+06 pCWX-EFs-GFP-mirGE CCR5-7-PGK-mCherry 1.21E+07 pCWX-EFs-GFP-mirGE CCR5-777-PGK-mCherry 1.27E+07 pCWX-EFs-mirGE CCR5-7-GFP-PGK-mCherry 6.82E+06 pCWX-EFs-mirGE CCR5-777-GFP-PGK-mCherry 4.75E+06 pCWX-EFs-No spacer-mirGE CCR5-777-PGK-mCherry 6.02E+06
(96) TABLE-US-00004 TABLE 4 Cloning primers Amplicon Primer forward 5′-3′ (AttB1-EcoRI) Primer reverse 5′-3′ (AttB2-XhoI) GFP GGGGACAAGTTTGTACAAAAAAGCAGGCTGAATT GGGGACCACTTTGTACAAGAAAGCTGGGTCTCG CTGAGCAAGGGCGAGGAGCTGT AGCTTGTACAGCTCGTCCATGCCG (SEQ ID NO: 1) (SEQ ID NO: 2) stopGFP GGGGACAAGTTTGTACAAAAAAGCAGGCTTCTAG GGGGACCACTTTGTACAAGAAAGCTGGGTCTCG AATGGATGTAAGTAGGTGAGTGAGCA AGCTTGTACAGCTCGTCCATGCCGAGA (SEQ ID NO: 3) (SEQ ID NO: 4) GFPpart1 GGGGACAAGTTTGTACAAAAAAGCAGGCTGAATT GGGGGCTCGAGTCGCCCTCGAACTTCACCTCG CTGAGCAAGGGCGAGGAGCTGT (SEQ ID NO: 6) (SEQ ID NO: 5) GFPpart2 GGGGGGAATTCCACCCTGGTGAACCGCATCGA GGGGACCACTTTGTACAAGAAAGCTGGGTCTCG (SEQ ID NO: 7) AGCTTGTACAGCTCGTCCATGCCG (SEQ ID NO: 8) INGFR GGGGACCACTTTGTACAAGAAAGCTGGGTCTCGA GGGGACAAGTTTGTACAAAAAAGCAGGCTGAAT GCTAGAGGATCCCCCTGTTCCACCT TCTCACCATGGGGGCAGGTGCCACCGG (SEQ ID NO: 9) (SEQ ID NO: 10) HO-1 GGGGACAAGTTTGTACAAAAAAGCAGGCTGAATT GGGGACCACTTTGTACAAGAAAGCTGGGTCTAC CTCACCATGGAGCGTCCGCAACCCGA AGCAACTGTCGCCACC (SEQ ID NO: 11) (SEQ ID NO: 12) CD4R1 GGGGACAAGTTTGTACAAAAAAGCAGGCTGAATT GGGGACCACTTTGTACAAGAAAGCTGGGTCTCG CTAATAGTGACCACTCCTGGCTAATTTTTGTATT AGGGTGAAACCCTTCTCTACTAAAAATACAAAA TTCAGTAGAGATAGGG TTAGCCGGGCACA (SEQ ID NO: 13) (SEQ ID NO: 14) CD4R2 — GGGGACCACTTTGTACAAGAAAGCTGGTCTCGA GCCGCACTCCAGCCTCGGCGACAGAGCAAGACT CTATCTCA (SEQ ID NO: 15) CD4R3 — GGGGACCACTTTGTACAAGAAAGCTGGGTCTCG AGTCGGGAGTACGAGACCAGCCTGGCCAACATA GTGAAATCC (SEQ ID NO: 16) H2B GGGGACAAGTTTGTACAAAAAAGCAGGCTGAATT GGGGACCACTTTGTACAAGAAAGCTGGGTCTCG CATGCCAGAGCCAGCGAAGTC AGGTGTACTTGGTGACGGCCTTA (SEQ ID NO: 17) (SEQ ID NO: 18) miRGE 1st CAGAAGGGGATCCATCGATACTAGTGGTGATAGC AGTAGCTTCTAGAGTAGAGTATGGTCAACCTTA hairpin AATGTCAGCAGTGCCT CTT (SEQ ID NO: 19) (SEQ ID NO: 20) miRGE 2nd CAGAAGGGGATCCGGTGATAGCAATGTCAGCAGT AGTAGCTACTAGTGTAGAGTATGGTCAACCTTA hairpin GCCT CTT (SEQ ID NO: 21) (SEQ ID NO: 22) miRGE 3rd CAGAAGGCTCGAGGGTGATAGCAATGTCAGCAGT AGTAGCTGGATCCGTAGAGTATGGTCAACCTTA hairpin GCCT CTT (SEQ ID NO: 23) (SEQ ID NO: 24)
(97) TABLE-US-00005 TABLE 5 miRGE hairpin components mir16-flanking GGTGATAGCAAT SEQ ID NO: 25 sequence Lower stem sequence CAGCAGTGCCT SEQ ID NO: 26 Lower stem sequence TCAGCAGTGCCT SEQ ID NO: 27 Lower stem sequence GTCAGCAGTGCCT SEQ ID NO: 28 Lower stem sequence CGTCAGCAGTGCCT SEQ ID NO: 29 Lower stem sequence ACGTCAGCAGTGCCT SEQ ID NO: 30 mir-30 loop sequence GTGAAGCCACAGATG SEQ ID NO: 31
(98) TABLE-US-00006 TABLE 6 miRGE backbone sequences Template 5′-3′ miRGE CCR5-7 GGT GAT AGC AAT GTC AGC AGT GCC TTC ATA GAT TGG ACT TGA CAC TTG TGA AGC CAC AGA TGA AGT GTC AAG CCC AAT CTA TGC AAG TAA GGT TGA CCA TAC TCT AC (SEQ ID NO: 32) miRGE GFP GGT GAT AGC AAT GTC AGC AGT GCC TAG TTC ACC TTG ATG CCG TTC TTG TGA AGC CAC AGA TGA AGA ACG GCA CCA AGG TGA ACC AAG TAA GGT TGA CCA TAC TCT AC (SEQ ID NO: 33) miRGE p22phox GGT GAT AGC AAT GTC AGC AGT GCC TAC ATG GCC CAC TCG ATC TGC CCG TGA AGC CAC AGA TGG GGC AGA TCG CGT GGG CCA TGC AAG TAA GGT TGA CCA TAC TCT AC (SEQ ID NO: 34)
(99) Lentiviral vector production and titration. Lentiviral vector stocks were generated using transient transfection of HEK 293T cells with the specific lentivector transfer plasmid, the psPAX2 plasmid encoding gag/pol and the pCAG-VSVG envelope plasmid, as previously described (Giry-Laterriere et al., 2011a, Giry-Laterriere et al., 2011a). Lentivector titration was performed using transduction of HT-1080 cells followed by flow cytometry quantification of mcherry-positive cells five days after transduction, as previously described (Giry-Laterriere et al., 2011a, Giry-Laterriere et al., 2011a).
(100) Cell culture and knockdown analysis. All cell lines were cultured in high glucose Dulbecco's modified eagle medium (Sigma) supplemented with 10% fetal calf serum, 1% Penicillin, 1% Streptomycin, and 1% L-glutamine. For each knockdown assay, cells were analyzed at least 5 days after transduction. For CCR5 knockdown studies, a subclone of HeLa-derived TZMb1 cells (AIDS Repository, Germantown, Md.), expressing high levels of human CCR5, named here HeLa R5, was used. For GFP knockdown, the same cells were used after GFP transduction at 1 copy of the vector and sorting of the GFP positive cells. CCR5 expression was detected using an anti-human CCR5-APC-antibody, (BD Pharmingen Cat. 550856) and flow cytometry analysis using FACS Cyan (Beckman Coulter). GFP expression was assessed on the same flow cytometer using GFP fluorescence median. Briefly, HeLa cells were transduced at 0.2 MOI with the miRGE-based knockdown vector to avoid the presence of a high copy number of the vector per cell and obtain comparable conditions. GFP or CCR5 expression was compared between the transduced and the remaining untransduced population of cells and expressed as a percentage of CCR5 expression relatively to the untransduced population.
(101) Real-time Quantitative Reverse Transcriptase Polymerase Chain Reaction. Cells or organotypic explant of organ of Corti were harvested and mRNA was extracted using Qiagen RNeasy mini kit following the manufacturer's instructions. RNA concentration was determined using a Nanodrop. 500 ng was used for cDNA synthesis using Takara PrimeScript RT reagent Kit following manufacturer's instruction. Real-time PCR was performed using SYBR green assay on a 7900HT SDS system from ABI. The efficiency of each primer was verified with serial dilutions of cDNA. Relative expression levels were calculated by normalization to the geometric mean of the two house-keeping genes GAPDH and EF1a and the GAG lentivector gene. The highest normalized relative quantity was arbitrarily designated as a value of 1.0. Fold changes were calculated from the quotient of means of these normalized quantities and reported as ±SEM. Sequences of the qPCR primers used are provided in Table 7.
(102) TABLE-US-00007 TABLE 7 qPCR primers Amplicon Primer forward 5′-3′ Primer reverse 5′-3′ Cyba (p22phox) TGGACGTTTCACACAGTGGT TGGACCCCTTTTTCCTCTTT (SEQ ID NO: 35) (SEQ ID NO: 36) miRGE pri-miRNA GGTGATAGCAATGTTCAGCAGTGCCT GTAGAGTATGGTCAACCTTACTT (SEQ ID NO: 37) (SEQ ID NO: 38) mature miRGE LNA modified proprietary sequence (exiqon) GAG GGAGCTAGAACGATTCGCAGTTA GGTTGTAGCTGTCCCAGTATTTGTC (SEQ ID NO: 39) (SEQ ID NO: 40) EEF1a TCCACTTGGTCGCTTTGCT CTTCTTGTCCACAGCTTTGATGA (SEQ ID NO: 41) (SEQ ID NO: 42) GAPDH TCCATGACAACTTTGGCATTG CAGTCTTCTGGGTGGCAGTGA (SEQ ID NO: 43) (SEQ ID NO: 44)
(103) Quantitative Reverse Transcriptase Polymerase Chain Reaction for mature miRNA detection. HeLa R5 cells were transduced at 0.2 MOI with lentivectors carrying the different SMIG. Transduced population (expressing mCherry) was sorted by FACS resulting in a homogeneous cell population carrying a single copy of the vector/cell. Total RNA was extracted using Trizol Reagent (Ambion) according to manufacturer instructions. RNA concentration was determined using a Nanodrop. 100 ng of RNA was used for the reverse transcription (miRCURY LNA™ miRNA PCR, Polyadenylation and cDNA synthesis kit (exiqon)). Reverse transcription was followed by real-time PCR amplification (ExiLENT SYBR® Green master mix kit (exiqon)) with LNA™ enhanced primers. Relative expression levels of the mature miRGE were calculated by normalization to the geometric mean of the two house-keeping miRNA (U6 and RNU5G). Fold changes were calculated from the quotient of means of these normalized quantities and reported as ±SEM. Sequences of the LNA™ enhanced primers were not provided by the manufacturer.
(104) Reactive Oxygen Species measurement by Amplex Red assay. PLB-985 cells were cultured in RPMI medium (Gibco), transduced as described above and differentiated into neutrophil-like cells during 5 days in presence of 1.25% DMSO. Levels of H2O2 produced by intact PLB-985 cells after stimulation of NOX2 with 100 nM phorbol myristate acetate (PMA) were then measured using Amplex Red fluorescence as previously described (Jaquet et al., 2011). Fluorescence was measured with a FluoSTAR OPTIMA, BMG labtech instrument at 37° C.
(105) Organotypic culture and transduction of rat organ of Corti. Three days old Wistar Rats were decapitated and the heads were cut sagittaly to remove the brain. The two otic capsules were isolated and transferred into ice-cold Hank's balanced salt solution (HBSS) (Invitrogen, USA) for sterile dissection under a binocular microscope (Nikon SMZ800, Japan) with forceps (World Precision Instruments, USA). After bone removal, the cochlea was transferred to a Transwell-Clear insert (6-well format, Corning, USA) with a permeable polyester membrane (0.4 μm pore size). The membranes were pre-coated with Celltak (Corning, USA) according to manufacturer's protocol. The organ of Corti (OC) was then separated from stria vascularis and the modiolus and plated on the insert, with the hair cells facing up. Dissection medium was carefully removed and 1.5 ml otic culture medium: (DMEM/F12 (Invitrogen, USA), 0.01% Ampicillin (Sigma, USA) and 10% fetal bovine serum (Invitrogen, USA) was added to the lower compartment under the insert membrane. On the following day, the medium on the insert was removed and they were transferred into an empty well. For the transduction, 200 μl otic culture medium was added on the explant together with 70 μl DMEM/F12 (Invitrogen/USA) containing 106, 5×106 or 107 particles of the stopGFP triple miRGE hairpin lentivector targeting p22phox. After 30 minutes of incubation at 37° C. and 5% C02, 1.5 ml otic culture medium was added to the lower compartment. The medium was replaced with fresh otic culture medium on the two following days. 5 days after the initial transduction, cochlear explants were either detached with trypsin for mRNA isolation or fixed for 10 minutes with 4% paraformaldehyde for immunostainings.
(106) Immunostaining and confocal microscopy of rat organotypic culture of organ of Corti. Cochlear explants were fixed with 4% paraformaldehyde for 10 minutes at room temperature. Explants were transferred (by cutting the insert membrane) to a 24 well plate, washed three times with PBS and permeabilized with 3% Triton-X 100 for 30 minutes. Cochlear explants were immersed in a blocking buffer containing 2% bovine serum albumin (BSA) and 0.01% Triton-X 100 for 1 hour at room temperature. Explants were incubated with the anti-MyoVIIa (1:500, rabbit; Proteus, USA) antibody in blocking buffer overnight at 4° C. On the following day, tissues were rinsed three times with PBS and incubated with the secondary antibody anti-rabbit Alexa Fluor 488 (1:500; Invitrogen, USA) in blocking buffer for 2 hours at room temperature. Explants were again washed 3 times with PBS and mounted on a glass slide with Fluoroshield containing DAPI (Sigma Aldrich, USA). The labelled cells were visualized with a confocal laser-scanning microscope (Zeiss LSM710) equipped with a CCD camera (Leica Microsystems) with a Planapochromat 10×/0.3 NA objective.
(107) Knockdown of CCR5 in humanized mice leukocytes. Human CD34 isolated from cord blood using magnetic beads (Miltenyi) were cultivated in activation medium (Cell Gro medium containing 20 ng/mL recombinant human [rh] stem cell factor (SCF), 20 ng/mL rh Flt3-L, 20 ng/mL rh interleukin-3 [IL-3], 20 ng/mL rh TPO1, 1% v/v penicillin-streptomycin [Penstrep]). The cells were seeded in a 24-well plate at 1.0_106 cells/mL for_24 h at 37_C in activation medium for pre-stimulation. On the next day for transduction, Lentiblast B was added to the medium in a dilution of 1:1,000. Used MOI for transduction was 50. One well with 0.1_106 cells was not transduced and served as negative control. CD34 cells were cultivated for 48 h and then harvested except the transduction controls. The cells designated for transplantation were frozen and stored until transplantation of newborn NGS mice in liquid N2. Newborn NGS mice were then irradiated with 1 Gy and then transplanted with 260,000 CD34+ cells. Week 23 after birth, engraftment check was done by analyzing peripheral blood from the mice. CCR5 expression was then investigated at 28 weeks old using the following antibodies: huCD45 FITC (304006), CD3 AF700 (300424), CD4 PE-CY7 (300512), CD8 BV421 (301036), and CCR5 APC (359122) (or isocontrol #400611) from BioLegend.
(108) Prediction of the minimum free energy of spacer sequences. The minimum free energy (MFE) of spacers was calculated using RNA fold web server (Institute for Theoretical Chemistry, University of Vienna, available on the world wide web at rna.tbi.univie.ac.at/cgi-bin/RNAWebSuite/RNAfold.cgi). To allow comparison of MFE between spacers, obtained values were divided by the length of the spacer.
(109) Calculation of the efficiency of concatenation of triple hairpin concatenates. The concatenation efficiency of triple hairpin constructs (E) was calculated according to the formula E=ln(CP)/ln(KP) where KP and CP are respectively the knockdown of CCR5 obtained with single and triple hairpin constructs. If E=3, a fully additive effect of the hairpins is observed in the concatenate. If E=1 the triple hairpin construct is as efficient as the single hairpin construct and no additive effect of the hairpins concatenation is observed.
(110) Statistical analysis. Statistical analyses were performed using GraphPad Prism 5.04 (GraphPad Software, La Jolla, Calif.). One-way analysis of variance followed by Bonferroni's multiple comparison tests, as well as t-tests (non-parametric, Mann-Whitney U-test).
Example 2—Results
(111) A spacer sequence is required for polymerase II promoter-driven miRNA mediated target gene knockdown. To optimize the miRGE-based knockdown and better understand the role of the spacer, the Green Fluorescent Protein (GFP) sequence was placed either on the 5′ or on the 3′-end of the miRGE hairpin sequences in a lentiviral vector (
(112) The efficacy of the spacer depends on its position. With the spacer between the promoter and the miRNA, an efficient CCR5 knockdown was observed with a single hairpin, which was markedly enhanced with a concatenated triple hairpin construct. When the spacer was put in the 3′ position of the miRNA gene, the single hairpin showed a decreased CCR5 knockdown efficiency, while the increased knockdown effect of the concatenate was entirely lost (
(113) Together, the data demonstrate that a spacer sequence—preferentially located in 5′ of the miRNA—is required to drive efficient knockdown via two types of polII-dependent promoters. The spacer is also required for additive effects of the hairpin concatenation (
(114) Efficiency of miRNA-based knockdown depends on the spacer sequence. The potency of several coding and noncoding spacer sequences was assessed (
(115) Table 8. Spacer Sequences and Biophysical Features
(116) In an attempt to identify specific regions within spacer sequences which have an effect on the knockdown efficiency, truncated forms of GFP (GPF1, GFP2) and of the iCD4 (iCD42, iCD43) were designed (
(117) TABLE-US-00008 Length Predicted MFE % Spacer (bp) Kcal/mol GC coding Comments Green Fluorescent 717 −264.6 61.11 YES Reference protein (GFP) spacer Truncated GFP1 369 −142.2 62.87 GFP2 388 −116.4 59.53 Stop codons in the 3 732 — — NO non coding reading frame after form the start codon of GFP (stopGFP) Microsomal Glutathion 726 −197.7 43.92 YES Resistance to Transferase-2 (MGST2) Busulfan Truncated form of the 843 −397.7 66.86 YES Pre- Nerve Growth Factor implantation Receptor (deltaNGFR) selection Heme Oxygenase (HO-1) 863 −336.2 61.24 YES Cytoprotection Histone2B (H2B) 378 −123.7 58.99 YES Neutral Amplicons from the 793 −235.9 46.71 NO Neutral? 1st intron of the CD4 gene iCD41 iCD42 620 −189.2 45.48 iCD43 380 −136 49.36
the knockdown efficiency (
(118) TABLE-US-00009 TABLE 9 Spacer sequences Spacer Sequence GFP ATGGATGTAAGTAGGTGAGTGAGCAAGGGCGAGGAGCTGTTCACCGGGGTGGTGCCCATCCTGGTCGAGCTGGACGG CGACGTAAACGGCCACAAGTTCAGCGTGTCCGGCGAGGGCGAGGGCGATGCCACCTACGGCAAGCTGACCCTGAAGT TCATCTGCACCACCGGCAAGCTGCCCGTGCCCTGGCCCACCCTCGTGACCACCCTGACCTACGGCGTGCAGTGCTTC AGCCGCTACCCCGACCACATGAAGCAGCACGACTTCTTCAAGTCCGCCATGCCCGAAGGCTACGTCCAGGAGCGCAC CATCTTCTTCAAGGACGACGGCAACTACAAGACCCGCGCCGAGGTGAAGTTCGAGGGCGACCACCCTGGTGAACCGC ATCGAGCTGAAGGGCATCGACTTCAAGGAGGACGGCAACATCCTGGGGCACAAGCTGGAGTACAACTACAACAGCCA CAACGTCTATATCATGGCCGACAAGCAGAAGAACGGCATCAAGGTGAACTTCAAGATCCGCCACAACATCGAGGACG GCAGCGTGCAGCTCGCCGACCACTACCAGCAGAACACCCCCATCGGCGACGGCCCCGTGCTGCTGCCCGACAACCAC TACCTGAGCACCCAGTCCGCCCTGAGCAAAGACCCCAACGAGAAGCGCGATCACATGGTCCTGCTGGAGTTCGTGAC CGCCGCCGGGATCACTCTCGGCATGGACGAGCTGTACAAGTAAAGCGGCCTGAATCGCCAGTGTC (SEQ ID NO: 46) stopGFP AATTCATGGATGTAAGTAGGTGAGTGAGCAAGGGCGAGGAGCTGTTCACCGGGGTGGTGCCCATCCTGGTCGAGCTG GACGGCGACGTAAACGGCCACAAGTTCAGCGTGTCCGGCGAGGGCGAGGGCGATGCCACCTACGGCAAGCTGACCCT GAAGTTCATCTGCACCACCGGCAAGCTGCCCGTGCCCTGGCCCACCCTCGTGACCACCCTGACCTACGGCGTGCAGT GCTTCAGCCGCTACCCCGACCACATGAAGCAGCACGACTTCTTCAAGTCCGCCATGCCCGAAGGCTACGTCCAGGAG CGCACCATCTTCTTCAAGGACGACGGCAACTACAAGACCCGCGCCGAGGTGAAGTTCGAGGGCGACACCCTGGTGAA CCGCATCGAGCTGAAGGGCATCGACTTCAAGGAGGACGGCAACATCCTGGGGCACAAGCTGGAGTACAACTACAACA GCCACAACGTCTATATCATGGCCGACAAGCAGAAGAACGGCATCAAGGTGAACTTCAAGATCCGCCACAACATCGAG GACGGCAGCGTGCAGCTCGCCGACCACTACCAGCAGAACACCCCCATCGGCGACGGCCCCGTGCTGCTGCCCGACAA CCACTACCTGAGCACCCAGTCCGCCCTGAGCAAAGACCCCAACGAGAAGCGCGATCACATGGTCCTGCTGGAGTTCG TGACCGCCGCCGGGATCACTCTCGGCATGGACGAGCTGTACAAGTAAAGCGGCCTGAATCGCCAGTGTC (SEQ ID NO: 47) GFP1 AATTCATGGATGTAAGTAGGTGAGTGAGCAAGGGCGAGGAGCTGTTCACCGGGGTGGTGCCCATCCTGGTCGAGCTG GACGGCGACGTAAACGGCCACAAGTTCAGCGTGTCCGGCGAGGGCGAGGGCGATGCCACCTACGGCAAGCTGACCCT GAAGTTCATCTGCACCACCGGCAAGCTGCCCGTGCCCTGGCCCACCCTCGTGACCACCCTGACCTACGGCGTGCAGT GCTTCAGCCGCTACCCCGACCACATGAAGCAGCACGACTTCTTCAAGTCCGCCATGCCCGAAGGCTACGTCCAGGAG CGCACCATCTTCTTCAAGGACGACGGCAACTACAAGACCCGCGCCGAGGTGAAGTTCGAGGGCGACC (SEQ ID NO: 48) GFP2 AATTCCACCCTGGTGAACCGCATCGAGCTGAAGGGCATCGACTTCAAGGAGGACGGCAACATCCTGGGGCACAAGCT GGAGTACAACTACAACAGCCACAACGTCTATATCATGGCCGACAAGCAGAAGAACGGCATCAAGGTGAACTTCAAGA TCCGCCACAACATCGAGGACGGCAGCGTGCAGCTCGCCGACCACTACCAGCAGAACACCCCCATCGGCGACGGCCCC GTGCTGCTGCCCGACAACCACTACCTGAGCACCCAGTCCGCCCTGAGCAAAGACCCCAACGAGAAGCGCGATCACAT GGTCCTGCTGGAGTTCGTGACCGCCGCCGGGATCACTCTCGGCATGGACGAGCTGTACAAGTAAAGCGGCCTGAATC GCCAGTGTC (SEQ ID NO: 49) H2B ATGCCAGAGCCAGCGAAGTCTGCTCCCGCCCCGAAAAAGGGCTCCAAGAAGGCGGTGACTAAGGCGCAGAAGAAAGG CGGCAAGAAGCGCAAGCGCAGCCGCAAGGAGAGCTATTCCATCTATGTGTACAAGGTTCTGAAGCAGGTCCACCCTG ACACCGGCATTTCGTCCAAGGCCATGGGCATCATGAATTCGTTTGTGAACGACATTTTCGAGCGCATCGCAGGTGAG GCTTCCCGCCTGGCGCATTACAACAAGCGCTCGACCATCACCTCCAGGGAGATCCAGACGGCCGTGCGCCTGCTGCT GCCTGGGGAGTTGGCCAAGCACGCCGTGTCCGAGGGTACTAAGGCCGTCACCAAGTACACCAGCGCTAAG (SEQ ID NO: 50) NGFR AATTCTCACCATGGGGGCAGGTGCCACCGGCCGCGCCATGGACGGGCCGCGCCTGCTGCTGTTGCTGCTTCTGGGGG TGTCCCTTGGAGGTGCCAAGGAGGCATGCCCCACAGGCCTGTACACACACAGCGGTGAGTGCTGCAAAGCCTGCAAC CTGGGCGAGGGTGTGGCCCAGCCTTGTGGAGCCAACCAGACCGTGTGTGAGCCCTGCCTGGACAGCGTGACGTTCTC CGACGTGGTGAGCGCGACCGAGCCGTGCAAGCCGTGCACCGAGTGCGTGGGGCTCCAGAGCATGTCGGCGCCGTGCG TGGAGGCCGACGACGCCGTGTGCCGCTGCGCCTACGGCTACTACCAGGATGAGACGACTGGGCGCTGCGAGGCGTGC CGCGTGTGCGAGGCGGGCTCGGGCCTCGTGTTCTCCTGCCAGGACAAGCAGAACACCGTGTGCGAGGAGTGCCCCGA CGGCACGTATTCCGACGAGGCCAACCACGTGGACCCGTGCCTGCCCTGCACCGTGTGCGAGGACACCGAGCGCCAGC TCCGCGAGTGCACACGCTGGGCCGACGCCGAGTGCGAGGAGATCCCTGGCCGTTGGATTACACGGTCCACACCCCCA GAGGGCTCGGACAGCACAGCCCCCAGCACCCAGGAGCCTGAGGCACCTCCAGAACAAGACCTCATAGCCAGCACGGT GGCAGGTGTGGTGACCACAGTGATGGGCAGCTCCCAGCCCGTGGTGACCCGAGGCACCACCGACAACCTCATCCCTG TCTATTGCTCCATCCTGGCTGCTGTGGTTGTGGGCCTTGTGGCCTACATAGCCTTCAAGAGGTGGAACAGGGGGATC CTCTAGC (SEQ ID NO: 51) MGST2 AATTCGGCACGAGGGACTTCTGTTCCAGAGCAAAGGTCATTCAGCCGCTTGAATCAGCCTTTTCCCCCCACCCGGTC CCCAACTTTGTTTACCCGATAAGGAAGGTCAGCATTCAAAGTCAAGAAGCGCCATTTATCTTCCCGTGCGCTCTACA AATAGTTCCGTGAGAAAGATGGCCGGGAACTCGATCCTGCTGGCTGCTGTCTCTATTCTCTCGGCCTGTCAGCAAAG TTATTTTGCTTTGCAAGTTGGAAAGGCAAGATTAAAATACAAAGTTACGCCCCCAGCAGTCACTGGGTCACCAGAGT TTGAGAGAGTATTTCGGGCACAACAAAACTGTGTGGAGTTTTATCCTATATTCATAATTACATTGTGGATGGCTGGG TGGTATTTCAACCAAGTTTTTGCTACTTGTCTGGGTCTGGTGTACATATATGGCCGTCACCTATACTTCTGGGGATA TTCAGAAGCTGCTAAAAAACGGATCACCGGTTTCCGACTGAGTCTGGGGATTTTGGCCTTGTTGACCCTCCTAGGTG CCCTGGGAATTGCAAACAGCTTTCTGGATGAATATCTGGACCTCAATATTGCCAAGAAACTGAGGCGGCAATTCTAA CTTTTTCTCTTCCCTTTAATGCTTGCAGAAGCTGTTCCCACCATGAAGGTAATATGGTATCATTTGTTAAATAAAAA TAAAGTCTTTATTCTGTTAAAAAAAAAAAAAAAAAAC (SEQ ID NO: 52) HO-1 AATTCATGGAGCGTCCGCAACCCGACAGCATGCCCCAGGATTTGTCAGAGGCCCTGAAGGAGGCCACCAAGGAGGTG CACACCCAGGCAGAGAATGCTGAGTTCATGAGGAACTTTCAGAAGGGCCAGGTGACCCGAGACGGCTTCAAGCTGGT GATGGCCTCCCTGTACCACATCTATGTGGCCCTGGAGGAGGAGATTGAGCGCAACAAGGAGAGCCCAGTCTTCGCCC CTGTCTACTTCCCAGAAGAGCTGCACCGCAAGGCTGCCCTGGAGCAGGACCTGGCCTTCTGGTACGGGCCCCGCTGG CAGGAGGTCATCCCCTACACACCAGCCATGCAGCGCTATGTGAAGCGGCTCCACGAGGTGGGGCGCACAGAGCCCGA GCTGCTGGTGGCCCACGCCTACACCCGCTACCTGGGTGACCTGTCTGGGGGCCAGGTGCTCAAAAAGATTGCCCAGA AAGCCCTGGACCTGCCCAGCTCTGGCGAGGGCCTGGCCTTCTTCACCTTCCCCAACATTGCCAGTGCCACCAAGTTC AAGCAGCTCTACCGCTCCCGCATGAACTCCCTGGAGATGACTCCCGCAGTCAGGCAGAGGGTGATAGAAGAGGCCAA GACTGCGTTCCTGCTCAACATCCAGCTCTTTGAGGAGTTGCAGGAGCTGCTGACCCATGACACCAAGGACCAGAGCC CCTCACGGGCACCAGGGCTTCGCCAGCGGGCCAGCAACAAAGTGCAAGATTCTGCCCCCGTGGAGACTCCCAGAGGG AAGCCCCCACTCAACACCCGCTCCCAGGCTCCGCTTCTCCGATGGGTCCTTACACTCAGCTTTCTGGTGGCGACAGT TGCTGTAGGGCTTTATGCCATGTGAC (SEQ ID NO: 53) iCD41 AATTCTAATAGTGACCACTCCTGGCTAATTTTTGTATTTTCAGTAGAGATAGGGTTTCACTATGTTGGCCAGGCTGG TCTCCAACTCCTGACCTAAAGTGATCCACCCACCTTGGTTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTG CCTGGACATATATCTATCTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGA TTTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACA GACGTGCGTCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTCACTATGTTGGCCAGGCTGGTCT CGTACTCCCGACCTCAGGTGATCCACTTGCCTTGGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACTGCATCC GGCCTTATATATCTATCTTGTCTGTCTGACTGTCTAATCTAATTCATCTATTTTATCTGTTTATCTTATCTATCATC TATTTATCTAATCTATCTGTCTGTATGTCTGTTTTTTTTTTGTTTTTTTTTTTTTTTTGAGATAGAGTCTTGCTCTG TCGCCGAGGCTGGAGTGCGGTGGCGCGATCTCAGCTCACTGCTGAACCTCCGCCTCCTGGGTTCTAAGCGATTCTCC TGCCTCAATCTTTGGAGTAGCTGGGATTACAGGCCCGTACCACTGTGCCCGGCTAATTTTGTATTTTTAGTAGAGAA GGGTTTCACCC (SEQ ID NO: 54) iCD42 AATTCTAATAGTGACCACTCCTGGCTAATTTTTGTATTTTCAGTAGAGATAGGGTTTCACTATGTTGGCCAGGCTGG TCTCCAACTCCTGACCTAAAGTGATCCACCCACCTTGGTTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTG CCTGGACATATATCTATCTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGA TTTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACA GACGTGCGTCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTCACTATGTTGGCCAGGCTGGTCT CGTACTCCCGACCTCAGGTGATCCACTTGCCTTGGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACTGCATCC GGCCTTATATATCTATCTTGTCTGTCTGACTGTCTAATCTAATTCATCTATTTTATCTGTTTATCTTATCTATCATC TATTTATCTAATCTATCTGTCTGTATGTCTGTTTTTTTTTTGTTTTTTTTTTTTTTTTGAGATAGAGTCTTGCTCTG TCGCCGAGGCTGGAGTGCGGC (SEQ ID NO: 55) iCD43 AATTCTAATAGTGACCACTCCTGGCTAATTTTTGTATTTTCAGTAGAGATAGGGTTTCACTATGTTGGCCAGGCTGG TCTCCAACTCCTGACCTAAAGTGATCCACCCACCTTGGTTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTG CCTGGACATATATCTATCTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGA TTTCGGCTCACTGCAACCTCCGC (SEQ ID NO: 56)
(119) The spacer sequence determines the additive effects of miRNA hairpin concatenation. To confirm the role of the spacer sequence in the concatenation potency of the vector, multi-hairpin constructs were designed with different spacers: GFP, GFP2, MGST2 or H2B (
(120) Translation-independent activity of the GFP spacer in cell lines and tissue explants. Among the tested candidates, the GFP sequence was most efficient as a spacer, both with respect to knockdown potency with a single hairpin and concatenation potency. Other coding sequences also yielded some significant knockdown activity, though the CD4 intron was inactive. A construct harboring stop codons in each possible reading frame was generated in order to test whether protein translation of GFP was required for optimal functioning of the SMIG (
(121) To demonstrate the therapeutic potential of the optimized SMIG including the stopGFP spacer, knockdown of the inner ear NADPH oxidase NOX3 was investigated, a potential therapeutic application. This reactive oxygen species (ROS)-producing NADPH oxidase has been shown to be a relevant source of ROS leading to inner ear damage, and it is hence an attractive knockdown target for inner ear protection.sup.26. A triple miRGE concatenate was designed, targeting the NOX3 subunit p22.sup.phox, under the control of the UBI promoter, and with stopGFP as a spacer. To identify transduced cells, the mCherry coding sequence under the control of the PGK promoter was also included in the construct. Newborn rat cochlear explants were transduced with this construct (
(122) Sustained miRNA-mediated knockdown of CCR5 in circulating leukocytes derived from human hematopoietic stem cells: To further demonstrate the in vivo efficacy and the therapeutic potential of the optimized SMIG including the stopGFP spacer, another promising clinical application was investigated, namely knockdown of the HIV co-receptor CCR5 in vivo (
(123) The spacer sequence regulates the steady state levels, but not the half-life of miRGE. PCR primers were designed to quantify unprocessed miRGE hairpins (pri-miRGE) (
(124) Maximizing concatenation and achieving multi-target gene knockdown. To further investigate the possibility of a multi-target gene knockdown vector with a single promoter-driven miRNA cluster, a fourth and a fifth mirGE hairpin, either targeting CCR5 or a second target gene (GFP in this case), was added to the triple CCR5 construct (
Example 3—Prophetic Synthetic Minigenes for Immune Checkpoint Knockdown
(125) Re-direction of immunotherapeutic cells with intrinsic immune checkpoint knockdown. Depicted in
(126) Tumor infiltrating lymphocytes with intrinsic immune checkpoint knockdown may be generated using the synthetic minigenes provided herein. To generate these TILs with immune checkpoint knockdown, TILs may be isolated from the patients' tumor tissue and purified. These purified TILs may be transduced with a lentiviral vector comprising a therapeutic minigene harboring miRNA hairpins directed to immune checkpoint mRNAs in order to knock down the gene expression of one or more immune checkpoints. Then, the modified TILs may be expanded ex vivo, and finally re-introduced to the patient.
(127) CAR T cells or TCR engineered T cells with intrinsic immune checkpoint knockdown may be generated similarly to TILs. T cells can be collected from patients by leukapheresis. The collected cells may then be transduced with a single vector comprising the miRNA hairpins targeting the immune checkpoint mRNAs as well as the CAR or engineered TCR sequence. Having these in a single vector, as shown in
Example 4—Synthetic Minigenes Target Gene Knockdown
(128) Single and Double Hairpin mirGE Constructs Knockdown CCR5 with High Efficiency in HeLaR5 Cells
(129) Using an optimized therapeutic minigene architecture (EF1s promoter, GFP2 spacer, single and double CCR5-targeting mirGE hairpins were constructed to evaluate how efficiently they could downregulate CCR5 relative to our established three-hairpin construct (
(130) Results indicated high efficiency downregulation of CCR5 with all three constructs, as demonstrated by significant reductions in MFI and an overall shift in fluorescent intensity when compared to cells transduced with the control vector (
(131) High Efficiency Knockdown of PD1 in Primary T Cells
(132) Considering the central role that PD1 plays in T exhaustion, and more broadly in the field of engineered T cell therapies, a therapeutic minigene was developed that would maximally downregulate PD1. Three mirGE constructs to silence PD1 were designed according the approach described previously (Myburgh et al., 2014, incorporated herein by reference). Target sequences were identified using online software tools, including i-Score Designer, BLOCK-iT (ThermoFisher), GeneScript siRNA Target Finder, and siDESIGN Center (Dharmacon). Based on the scoring of these tools, a list of top 10 target sequences was generated. The target sequences were then each screened for homology across the human genome using BLAST, and those with >70% homology to any other gene were excluded. Finally, three target sequences were selected (Table 10) for cloning into the mirGE and our optimized therapeutic minigene architecture (EF1s promoter, GFP2 spacer). Once constructed, the three minigenes were packaged into lentiviral vectors and used to transduce primary T cells from two healthy donors at a MOI of 1.0 and 2.5. All constructs also carried a mCherry reported gene to identify transduced cells. PD1 expression levels were measured 5-7 days after transduction using flow cytometry. Since PD1 is not expressed uniformly, nor constitutively on primary T cells, we first determined the percentage of PD1-expressing T cells, and then compared the MFI of the PD1-expressing cells relative to control transduced (mCherry only) T cells.
(133) TABLE-US-00010 TABLE 10 PD1 target sequences Identifier Target sequence PD1-1A (SEQ ID NO: 59) CGGAGAGCTTCGTGCTAAA PD1-2A (SEQ ID NO: 60) CCAACACATCGGAGAGCTT PD1-3A (SEQ ID NO: 61) CCAGCAACCAGACGGACAA
(134) The initial screen for target sequences which could be accessible for mirGE knockdown resulted in one of the three candidates showing significant effect (PD1-1A). As can be seen in examples of the flow cytometry dot plots and histograms (
(135) Thus, the PD1-1A mirGE was applied for further development of two and three hairpin constructs in an attempt to achieve maximal knockdown of PD1 (
(136) PD1 Knockdown in CAR T Cells Protects Against T Cell Exhaustion
(137) To evaluate if PD1-targeting constructs would be protected against T cell exhaustion, anti-cKit CAR T cells transduced and co-cultured these cells with HL-60 tumor cells at effector:target (E:T) ratios of 1:15 and 1:30 over a four day period. A pure population of anti-cKit CAR T cells (previously selected) were thawed and transduced 24 hours later at a MOI of 1.0 with lentivectors carrying a three-hairpin mirGE therapeutic minigene against PD1. Co-culturing was initiated with 100,000 CAR T cells (anti-cKit with and without PD1 knockdown), and 1.5 million and 3.0 million HL-60 tumor cells added to achieve the 1:15 and 1:30 E:T ratios, respectively. A negative control group of CAR T cells only (not co-cultured with target cells) was also included. All conditions were cultured in medium not containing IL-2, made up with Advanced RPMI, 10% FBS, 1% pen-strep and 1× glutamax. After four days of co-culturing, cells were harvested for counting and flow cytometric analysis of PD1 expression on CD3 positive T cells.
(138) A transduction rate of ˜20% was achieved in the anti-cKit CAR T cells transduced with our PD1-targeting therapeutic minigene (based on mCherry positivity). On Day 4, the transduction rate was assessed again in the negative control group, which was reported to be 18.6% (
(139) PD1 knockdown in mCherry transduced CAR T cells was confirmed via flow cytometric analysis (
(140) Multi-Target mirGE Hairpins Maintain Efficiency of CCR5 Knockdown
(141) To evaluate if up to six mirGE hairpins could be expressed with optimized therapeutic minigene architecture (EF1s promoter, GFP2 spacer), a multi-target hairpin construct against PD1, GFP and CCR5 was constructed (
(142) Four Hairpin Therapeutic Minigenes Effectively Downregulate PD1 and CCR5 in Primary T Cells
(143) Using a four-hairpin mirGE construct (two hairpins against PD1, two against CCR5), primary T cells were transduced as described before and evaluated for knockdown of these two clinically relevant target genes. Five days after transduction, PD1 and CCR5 expression was assessed via flow cytometry (
(144) All of the methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions and methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the invention. More specifically, it will be apparent that certain agents which are both chemically and physiologically related may be substituted for the agents described herein while the same or similar results would be achieved. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention as defined by the appended claims.
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