NIPAH VIRUS ENVELOPE PSEUDOTYPED LENTIVIRUSES AND METHODS OF THEIR USE

Abstract

The present invention relates to lentiviral particles which have been pseudotyped with Nipah virus (NiV) fusion (F) and attachment (G) glycoproteins (NiVpp-F/G). Additionally, the present invention relates to truncated NiV-F glyocproteins useful in producing such NiVpp lentiviral particles, as well as to additional variant peptides which enhance activity. Further, the present invention relates to methods of using such lentiviral particles or sequences, for example in the treatment of cancer or CNS disorders.

Claims

1.-11. (canceled)

12. A method for specifically targeting a desired nucleic acid to ephrin B2 expressing cells, the method comprising contacting a Nipah virus (NiV) envelope pseudotyped lentivirus particle with ephrin B2 expressing cells, or administering the NiV pseudotyped lentivirus particle to a subject organism possessing ephrin B2 expressing cells, wherein the NiV pseudotyped lentivirus particle comprises NiV fusion (NiV-F) and attachment (NiV-G) glycoproteins, wherein the NiV-F glycoprotein has a cytoplasmic tail truncation consisting of deletion of amino acid residues 525-544 of SEQ ID NO: 1 NiV-F (T234 truncation) and a mutation to an N-linked glycosylation site, wherein the Niv-G glycoprotein is a wild type Niv-G or a truncated Niv-G selected from the group consisting of the amino acid SEQ ID NOS: 13, 15, 17, 19, 21 and 23, wherein the lentivirus infects cells expressing Ephrin B2 or Ephrin B3 receptors; and wherein the pseudotyped lentivirus particle further comprises the desired nucleic acid.

13. The method of claim 12, wherein the NiV pseudotyped lentivirus particle is administered to a subject organism possessing ephrin B2 expressing cells, wherein the pseudotyped lentivirus further comprises a desired nucleic acid effective for treating cancer.

14. The method of claim 12, wherein the NiV pseudotyped lentivirus particle is administered to a subject organism possessing ephrin B2 expressing tumors, wherein the pseudotyped lentivirus further comprises a desired nucleic acid effective for inhibiting tumor growth.

15. The method of claim 12, wherein the NiV pseudotyped lentivirus particle is administered to a subject organism possessing ephrin B2 expressing tumor angiogenic vessels, wherein the pseudotyped lentivirus further comprises a desired nucleic acid effective against angiogenic vessels.

16. A method for delivering a desired nucleic acid across crossing the blood brain barrier, the method comprising administering to a subject organism a NiV pseudotyped lentivirus particle, wherein the NiV pseudotyped lentivirus particle comprises NiV fusion (NiV-F) and attachment (NiV-G) glycoproteins, wherein the NiV-F glycoprotein has a cytoplasmic tail truncation consisting of deletion of amino acid residues 525-544 of SEQ ID NO: 1 NiV-F (T234 truncation) and a mutation to an N-linked glycosylation site, wherein the Niv-G glycoprotein is a wild type Niv-G or a truncated Niv-G selected from the group consisting of the amino acid SEQ ID NOS: 13, 15, 17, 19, 21 and 23, wherein the lentivirus infects cells expressing Ephrin B2 or Ephrin B3 receptors; and wherein the pseudotyped lentivirus particle further comprises the desired nucleic acid.

17. The method of claim 16, wherein the desired nucleic acid comprises one or more therapeutic genes.

18. A method for altering brain function in a subject, the method comprising injecting a NiV pseudotyped lentivirus particle into specific areas of said subject's brain, wherein the NiV pseudotyped lentivirus particle comprises NiV fusion (NiV-F) and attachment (NiV-G) glycoproteins, wherein the NiV-F glycoprotein has a cytoplasmic tail truncation consisting of deletion of amino acid residues 525-544 of SEQ ID NO: 1 NiV-F (T234 truncation) and a mutation to an N-linked glycosylation site, wherein the Niv-G glycoprotein is a wild type Niv-G or a truncated Niv-G selected from the group consisting of the amino acid SEQ ID NOS: 13, 15, 17, 19, 21 and 23, wherein the lentivirus infects cells expressing Ephrin B2 or Ephrin B3 receptors; and wherein the pseudotyped lentivirus further comprises a desired nucleic acid effective for altering brain function.

19. The method of claim 12, wherein the cells are neurons or endothelial cells that overexpress ephrinB2.

20. The method of claim 12, wherein the cells are ephrin B2 positive embryonic, neural, and/or hematopoietic cell populations.

21. The method of claim 12, wherein the mutation to an N-linked glycosylation site comprises a substitution of glutamine for asparagine at amino acid position 99 of SEQ ID NO: 1 (DeltaN3 mutation).

22. The method of claim 16, wherein the mutation to an N-linked glycosylation site comprises a substitution of glutamine for asparagine at amino acid position 99 of SEQ ID NO: 1 (DeltaN3 mutation).

23. The method of claim 18, wherein the mutation to an N-linked glycosylation site comprises a substitution of glutamine for asparagine at amino acid position 99 of SEQ ID NO: 1 (DeltaN3 mutation).

Description

BRIEF DESCRIPTION OF THE FIGURES

[0026] This application file contains at least one drawing executed in color. Copies of this application with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.

[0027] FIG. 1 shows relevant portions of the NiV-F and NiV-G glycoproteins and the mutations made thereto.

[0028] FIG. 2 shows the titer obtained from NiVpp pseudotyped lentivirus produced using various NiV-F and NiV-G truncated glycoproteins.

[0029] FIG. 3 shows the relative infection of various cell types by various forms of NiVpp pseudotyped lentivirus, in some cases in the presence of soluble ephrinB2. In some panels, infectivity of VSV-G is also shown.

[0030] FIG. 4 shows the ability of NiVpp pseudotyped lentivirus to infect various cell types at various MOIs., in some cases in the presence of soluble ephrinB2.

[0031] FIG. 5 shows the selectivity index of various pseudotypes of lentivirus for ephrinB2+ cells, when those cells are co-cultured with ephrinB2− cells at different ratios (1:1, 1:10, 1:100, and 1:1000).

[0032] FIGS. 6 and 7 show the localization of various lentivirus pseudotypes when they are injected into the animal for an in vivo examination of infectivity.

DETAILED DESCRIPTION

[0033] Before describing the present invention in detail, it is to be understood that this invention is not limited to particular embodiments, which can, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting. Unless defined otherwise, all technical and scientific terms used herein generally have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Generally, the nomenclature used herein and the laboratory procedures in cell culture, molecular genetics, organic chemistry, and nucleic acid chemistry and hybridization are those well-known and commonly employed in the art. Standard techniques are used for nucleic acid and polypeptide synthesis. Procedures used for genetic engineering are well known and can be found, for example, in Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor, N.Y.).

[0034] As used in this specification and the appended claims, terms in the singular and the singular forms “a,” “an,” and “the,” for example, include plural referents unless the content clearly dictates otherwise. Thus, for example, reference to “polypeptide,” “the polypeptide” or “a polypeptide” also includes a plurality of polypeptides. Additionally, as used herein, the term “comprises” is intended to indicate a non-exhaustive list of components or steps, thus indicating that the given composition or method includes the listed components or steps and may also include additional components or steps not specifically listed. As an example, a composition “comprising a polypeptide” may also include additional components or polypeptides. The term “comprising” is also intended to encompass embodiments “consisting essentially of” and “consisting of” the listed components or steps. Similarly, the term “consisting essentially of” is also intended to encompass embodiments “consisting of” the listed components or steps.

[0035] Numeric ranges recited within the specification are inclusive of the numbers defining the range (the end point numbers) and also are intended to include each integer or any non-integer fraction within the defined range.

[0036] In describing and claiming the present invention, the following terminology will be used in accordance with the definitions set out below.

[0037] The terms “polypeptide,” “peptide,” and “protein” are generally used interchangeably herein and they refer to a polymer in which the monomers are amino acids that are joined together through amide bonds. Additionally, unnatural amino acids, for example, β-alanine, phenylglycine, and homoarginine are also included. Amino acids that are not gene-encoded can also be used with the technology disclosed herein. Furthermore, amino acids that have been modified to include reactive groups, glycosylation sites, polymers, therapeutic moieties, biomolecules, and the like can also be used. All of the amino acids used herein can be either the D- or L-isomer. The L-isomer is generally preferred. As used herein, “polypeptide,” “peptide,” and “protein” refer to both glycosylated and unglycosylated forms.

[0038] The term “amino acid” refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function in a manner similar to the naturally occurring amino acids. Naturally occurring amino acids are those encoded by the genetic code, as well as those amino acids that are later modified, e.g., hydroxyproline, γ-carboxyglutamate, and O-phosphoserine. “Amino acid analogs” refers to compounds that have the same basic chemical structure as a naturally occurring amino acid, i.e., an α carbon that is bound to a hydrogen, a carboxyl group, an amino group, and an R group, e.g. homoserine, norleucine, methionine sulfoxide, methionine methyl sulfonium. Such analogs have modified R groups (e.g., norleucine) or modified peptide backbones, but retain the same basic chemical structure as a naturally occurring amino acid. “Amino acid mimetics” refers to chemical compounds that have a structure that is different from the general chemical structure of an amino acid, but that function in a manner similar to a naturally occurring amino acid.

[0039] As used herein, “NiVpp,” “NiVpp lentivirus,” “NiVpp pseudotyped lentivirus,” NiV pseudotyped lentivirus,” or the like refers to a lentivirus particle which has been pseudotyped using Nipah virus envelope glycoproteins NiV-F and NiV-G. The NiV-F glycoprotein on such NiVpp lentivirus particles is a variant form which has been modified such that it possesses a cytoplasmic tail truncation. In certain examples, the truncation will be a deletion of amino acid residues 525-544 of the NiV-F peptide, which will be referred to herein as the “T5F” or “T234F” form of the NiV-F glycoprotein (see FIG. 1). In other examples, the NiV-F glycoprotein will further include a mutation to an N-linked glycosylation site, more specifically a substitution of glutamine (Q) for asparagine (N) at amino acid position 99 of the NiV-F peptide, which will be referred to herein as the “DeltaN3” or “ΔN3” form of the NiV-F glycoprotein. The NiV-G glycoprotein can be either a wild-type form or a modified or variant form of the protein, such as a truncated NiV-G. Deletions of 5, 10, 15, 20, 25, and 30 amino acids at or near the N-terminus of the NiV-G peptide were constructed, which are referred to herein as “Δ5G,” “Δ10G,” “Δ15G,” “Δ20G,” “Δ25G,” and “Δ30G,” respectively. A partial amino acid sequence of the NiV-F and NiV-G peptides showing each one of these variations is shown in FIG. 1.

[0040] The present inventors engineered the Nipah virus envelope glycoproteins to be efficiently pseudotyped onto lentiviruses, and such NiV pseudotyped lentiviruses can efficiently target ephrinB2 expressing cells in vitro and in vivo. In certain examples, the NiVpp can be used to target a subpopulation of ephrinB2+/SSEA-430 human embryonic stem cells (hESC). In other examples, NiVpp can be used to deliver agents that antagonize EphB-ephrinB2 mediated signaling specifically to ephrinB2-expressing target cells.

[0041] Further, NiVpp is the first demonstration of any lentiviral vector administered intravenously that can bypass the liver sink, which allows for targeting of specific ephrinB2+ populations in vivo. In addition, the natural tropism of NiVpp can be altered by mutating the natural receptor binding site to make it more ephrinB2 or B3 specific, depending on the clinical context of its use. NiVpp opens up the possibility for therapeutic targeting of ephrinB2-overexpressing cells common in various solid cancers or their tumor angiogenic vessels (see E. Pasquale, 2011). EphrinB2 and its endogenous receptor, EphB4, are both receptor tyrosine kinases that undergo bi-directional signaling as well as bidirectional endocytosis upon interaction with each other. NiVpp can take advantage of this biological property for transcytosis across the blood brain barrier. This is a critical barrier in CNS targeted gene therapy (by systemic administration). NiVpp can transcytose across functional microvascular endothelial cell layers to infect target cells at the bottom of the transwell chamber. Further, considering that NiVpp can transduce Nestin+ neural stem cells even more efficiently than VSV-Gpp, direct stereotatic injection of NiVpp into specific CNS areas where neurogenesis (proliferation of neurons from stem cell progenitors) is known to occur in the adult brain, such as the hippocampus and the subventricular zone, is possible.

[0042] The efficiency of NiVpp transduction can be improved by engineering hyperfusogenic mutations in one or both of NiV-F and NiV-G. Several such mutations have been previously described (see, e.g., Lee at al, 2011, Trends in Microbiology). This could be useful, for example, for maintaining the specificity and picomolar affinity of NiV-G for ephrinB2 and/or B3 while independently enhancing the entry efficiency of NiVpp. Additionally, mutations in NiV-G that completely abrogate ephrinB2 and B3 binding, but that do not impact the association of this NiV-G with NiV-F, have been identified. This could allow for specific targeting of other desired cell types that are not ephrinB2+ through the addition of a single chain variable fragment (scFV) directed against a different cell surface molecule

[0043] The inventors have generated several mutants of the NiV fusion protein (NiV-F), and have also generated stepwise truncations in the cytoplasmic tail of the attachment protein (NiV-G), and screened each in combination with the NiV-F variant(s) for the ability to pseudotype lentivirus. Infectivity has been examined using a variety of cell types, including 293T and CHO-B2 cells, both of which express the NiV primary receptor, ephrinB2. While many of the G-truncations were expressed and could be pseudotyped onto lentiviruses, the highest increase in viral transduction titers (˜100-fold) was obtained with the NiV-F variant and wild-type NiV-G, indicating that only truncations in the cytoplasmic tail of NiV-F are critical for efficient pseudotyping. Infection was blocked using soluble ephrinB2, confirming specificity of NiV pseudotyped lentivirus for ephrinB2+ cells. Moreover, NiV pseudotyped lentiviruses can suitably transduce primary human neurons and microvascular endothelial cells. Thus, lentivirus pseudotyped with NiV envelope may be used for targeted gene therapy in situations where ephrinB2/B3 is upregulated in the diseased tissue, thereby overcoming limitations of current gene therapy.

[0044] The NiVpp psuedotyped lentivirus vectors disclosed herein could be used to deliver any desired nucleic acid encoding for any desired peptide to any cell that expresses an appropriate receptor for NiV. In certain examples, these nucleic acid “payloads” will be delivered to cells expressing ephrin, for example ephrinB2 or ephrin B3. In other examples, the payload may be a nucleic acid encoding for a peptide product that is absent from the gene, such as is commonly done in gene therapy. This could be useful, for example, for targeting a genetic payload to neural stem cells. In other examples, the payload may be a nucleic acid or peptide that is toxic to the cell, for example to combat cancer cells. In other examples, the payload may be an ephrin antagonist, such as a soluble ephrinB2 or a nucleic acid capable of silencing or downregulating ephrinB2, such as an siRNA. Delivery of such ephrinB2 antagonists may be useful, for example, for impacting cell pluripotency or development, or for decreasing metastasis of certain cancer cells.

[0045] The following examples are offered to illustrate, but not to limit, the claimed embodiments. It is to be understood that the examples and embodiments described herein are for illustrative purposes only, and persons skilled in the art will recognize various parameters that can be altered without departing from the spirit of the disclosure or the scope of the appended claims.

EXAMPLES

Example 1

Generation of Truncated Glycoproteins and NiVpp Pseudotyped Lentivirus

[0046] Previous studies have shown that pseudotyping of lentiviral vectors with unmodified paramyxoviral glycoproteins is highly inefficient. In the present study, we obtained chemically-synthesized, codon-optimized wild-type NiV-F and NiV-G nucleotides. These codon-optimized NiV-F and NiV-G sequences included a tag at the 3′ end encoding an AU1 peptide tag (DTYRYI) or a hemaglutinin peptide tag (YPYDVPDYA), respectively. These were subcloned into pcDNA3.1 vectors for mutagenesis. Variants of NiV-F and NiV-G were produced using a QuickChange site directed mutagenesis kit (Stratagene, Cedar Creek, Tex.) with primers designed to correspond to the desired deletions. A NiV-F variant, termed T5F or T234F, with a truncation of the cytoplasmic tail, as discussed above, was produced (see, e.g., Aguilar et al. (2007) J. Virol. 81:4520-4532). NiV-G variants were produced by making stepwise truncations of the cytoplasmic tail of NiV-G. FIG. 1 shows the variant forms of NiV-F and NiV-G that were produced.

[0047] NiVpp lentiviral vectors were created using various combinations of these variant NiV-F and NiV-G glycoproteins. All lentiviral vectors were produced by calcium phosphate-mediated transient transfection of 293T cells. One day prior to transfection, 1.6×10.sup.7 293T cells were seeded in a T175 flask. 7pg of NiV-F (wild-type of variant), 7 μg of NiV-G (wild-type or variant), 12.5 μg of the packaging plasmid pCMVΔR8.9, and 12.5 μg of the lentiviral transfer vector plasmid FG12-GFP or FUhLucW were transfected into cells. After 8 h, the transfection medium was removed and fresh medium was added. 48 h post-transfection, the viral supernatant was harvested and concentrated by centrifugation at 28,000rpm at 4° C. for 2 h over a 20% sucrose cushion. To determine viral titer, serial dilutions of concentrated viral stocks were added to 293T cells and incubated at 37° C. for 2 h. 3 days post-infection, the cells were analyzed by flow cytometry for eGFP expression. Titers are expressed as infectious units per mL (IU/mL).

[0048] Truncation of the NiV-F cytoplasmic tail alone resulted in a titer of ˜10.sup.6 IU/mL on 293T cells, a 100-fold increase in titer compared to wtF/wtG pseudotypes (FIG. 2). With regard to the NiV-G variants, although the T234F/Δ10G and T234F/Δ25G variants demonstrated similar titers to T234F/wtG, none of the NiV-G variants produced greater titers than T234F/wtG (FIG. 2). Moreover, combinations of wt F with the NiV-G truncation variants produced extremely low titers (data not shown), indicating that truncations in NiV-F are critical for efficient pseudotyping. Following concentration, titers of ˜10.sup.8-10.sup.9 were obtained, compared to 10.sup.10 for VSV-G (data not shown). These high titer NiV pseudotyped lentiviruses can be used for efficient infection of ephrinB2+ cells, including for infection of hESCs, to deliver marker genes to tag ephrinB2+ hESCs, or to deliver siRNAs or other genes to antagonize the ephrinB2-ephB4 axis on hESCs.

Example 2

In Vitro and In Vivo Infection Using NiVpp Pseudotyped Lentivirus

[0049] Increasing amounts of virus (based on MOI or p24 equivalent) were added to 1×10.sup.5 cells of each cell type and centrifuged at 2,000 rpm at 37° C. for 2 hours. As a specificity control, 10 nM of soluble ephrinB2 (R&D Systems) was added to the infection medium in some studies. To exclude pseudotransduction, 5 μM of nevirapine (NVP; a reverse transcriptase inhibitor) was added in some studies. For stem cell transductions, 4 ng/ml of polybrene (Sigma) was added. Following an overnight incubation with virus, the infection medium was removed and replaced with fresh medium. 72 hours post-infection, the cells were harvested and analyzed by flow cytometry for eGFP expression. For transduction of a mixed population of cells, ephrinB2+ human U87 cells were mixed with ephrinB2− non-human Chinese hamster ovary (CHO) cells at different ratios (U87:CHO ratios=1:1, 1:10, 1:100, and 1:1000), and seeded at a density of 50,000 cells per well in 24-well plates. The next day, cells were infected with 1 or 10 ng of NiV T5F/wt G, T5FΔN3/wt G, and VSV-G pseudotypes. 72 h post-infection, the cells were harvested, stained with the mouse W6/32 anti-human HLA-ABC monoclonal antibody (eBioscience), followed by Alexa 647-conjugated goat anti-mouse secondary antibodies. Samples were fixed and then analyzed by dual-color flow cytometry for human HLA and eGFP expression.

[0050] CHO, CHO-B2, and CHO-B3 cells were infected with 0.01 ng, 0.1 ng, and 1 ng (p24 equivalents) of NiVpp or VSV-Gpp lentiviral pseudotypes carrying the GFP reporter gene (FIG. 3, panels A-D). Infectivity was determined by the percent of GFP+ cells at 48 h post-infection via FACS analysis. The % GFP+ cells in each of the CHO cell lines infected by VSV-Gpp at maximal viral input (1 ng) was set at 100%, and all other infections in that cell line were normalized to this value. For reference, at 1 ng, VSV-G infected 20.2% of CHO, 22.7% of CHO-B2, and 21.6% of CHO-B3 cells. U87 cells and HMVECs were infected with T5F/wt G and T5FΔN3/wt G pseudotypes as described for panels A-C but normalized to VSV-Gpp infection of the same cell line (U87 or HMVECs) at maximal viral input (1 ng) (FIG. 3, panels E & F). For reference, at 1 ng, VSV-G infected 36.5% of U87 cells and 14.4% of HMVECs. Inhibition by 10 nM of soluble ephrinB2 (sEFNB2) was used to demonstrate specificity of NiV receptor-mediated entry. All pseudotyped particle infections, regardless of envelope used, were also abrogated by 5 μM niverapine (NVP), a reverse transcriptase inhibitor (data not shown). Data shown in FIG. 3 are averages±standard deviations for three independent experiments. Statistical analyses were performed using a two-way ANOVA with Bonferroni post-test comparison using GraphPad PRISM™. *: p<0.05, **: p<0.01, ****: p<0.0001. As this figure demonstrates, NiVpp pseudotyped lentivirus is able to effectively infect all cell types tested in an ephrinB2 dependent manner. Moreover, T5FΔN3 showed an improved infectivity versus T5F.

[0051] EphrinB2 is a functional marker of human embryonic, neural, and hematopoietic stem cells (hESC, hNSC and hHSC). To confirm that ephrinB2 is functionally expressed on hESC, hNSC and hHSC, and to confirm that T234F/wtG pseudotype can mediate transfer into these ephrinB2+ cells, we transduced human ESCs, HSCs, and NSCs with NiVpp pseudotyped lentiviruses carrying a marker gene for EGFP. FIG. 4 shows that NiV pseudotypes infected SSEA-4+ hESC (H1 line) (panel A), hNSC (Nestin+) (panel B), and a subpopulation of purified CD34+ cells from human fetal liver (panel C). More specifically, in panel A of FIG. 4, increasing amounts of NiVpp were added to H9 hESCs. Cells were stained for the cell-surface pluripotency marker, SSEA-4, and examined for GFP expression 72 h post-transduction by FACS analysis. 1×10.sup.8 IU of NiVpp produced an infection rate of approximately 36% of SSEA-4+ hESC (FIG. 4, panel A). For panel B of FIG. 4, progenitor cells derived from the medial temporal lobe of a 17-week human fetus were infected with NiVpp. 72 h post-transduction, cells were stained for nestin and GFP expression was quantified by FACS analysis. The results of this analysis suggest that the NiV pseudotypes may infect NSC more efficiently than VSV-G pseudotypes. In panel C of FIG. 4, purified CD34.sup.+ cells from human fetal liver were infected with NiVpp. 72 h post-transduction, cells were stained for the cell-surface marker CD34 and analyzed for GFP expression by FACS analysis. At a multiplicity of infection (MOI) of 10, T234F/wtG pseudotypes specifically transduced ˜12% of purified CD34+ cells from human fetal liver. Moreover, this infection was inhibited with soluble ephrinB2 (10 nM) in all cases (data only shown for fetal liver CD34+ cells, which shows a reduction from ˜12% to <1% infection in the presence of soluble ephrinB2).

[0052] In the ehprinB2+/B2− ratio study, U87 (ephrinB2+) cells were mixed with CHO (ephrinB2−) cells at different ratios (U87:CHO ratios=1:1, 1:10, 1:100, and 1:1000) and seeded at a density of 50,000 cells per well in 24-well plates. The next day, cells were infected with 1 or 10 ng of NiV T5F/wt G, T5FΔN3/wt G, and VSV-G pseudotypes. 72 h post-infection, the cells were harvested and stained with the

[0053] W6/32 anti-human HLA-ABC monoclonal antibody and the infection rate (GFP-positive cells) was determined by FACS analysis. Although the cells were seeded and infected at the indicated ratio, the CHO cells divided faster and outgrew the U87 cells by about ten-fold in each sample. Data from 300,000 cells were acquired for every condition used for analysis. To take into account the differential permissivity of U87 and CHO cells to lentiviral transduction, we first calculated the “cell-specific selectivity index” for U87 cells, the U87 SI as {B/(A+B)}/{D/(C+D)} where B and D represents the % of infected (GFP+) U87 and CHO cells, respectively, and A and C represents their uninfected counterparts, such that the total fraction of U87 (A+B) and CHO (C+D) cells in any given admixture upon analysis must equal 100%. A U87 SI of >1 indicates a selective preference for infecting U87 over CHO cells. For VSV-Gpp, the U87 SI at 1 and 10 ng is 5.14 and 1.93, respectively. This likely reflects the receptor-independent preference for U87 over CHO cells due to the HIV-1 based vector backbone alone. The reduction in U87 SI at a higher inoculum of VSV-Gpp is also consistent with the known ability of VSV-G-delivered gag to saturate non-human post-entry restriction factors. Since VSV-G is not known to have a cell-type specific receptor, we calculated the “NiV receptor-specific selectivity index”, or the “EphrinB2 SI” as the VSV-G or NiV Env specific U87 SI divided by the U87 SI for VSV-G. This normalizes for differences in the intrinsic permissiveness of U87 over CHO cells for lentiviral transduction. This formulation now allows one to evaluate the selectivity of NiVpp for infecting ephrinB2-expressing cells relative to VSV-Gpp under all conditions analysed. The values of the U87 SI and EphrinB2 SI for VSV-G, T5F, and T5FΔN3 pseudotypes are provided in Table 1:

TABLE-US-00001 TABLE 1 Specificity Index Infection rate VSV-G T5F T5FΔN3 U87 SI 1 ng 5.14 258.7 292.5 U87 SI 10 ng 1.93 362.8 342.9 EphrinB2 SI 1 ng 1.00 50.3 56.9 Ephrin B2 SI 10 ng 1.00 188.0 177.7

[0054] The EphrinB2 Selectivity Index calculated for VSV-Gpp, and NiVpp bearing T5F or T5F-ΔN3 for all the indicated conditions is shown in FIG. 5. Data shown are averages±standard deviations for triplicates done at 1 ng, and average±range for duplicates done at 10 ng. As these results demonstrate, the NiVpp pseudotyped lentivirus vectors have a greatly increased specificity for EphrinB2 bearing cells as compared to VSV-Gpp pseudotyped lentivirus.

[0055] For in vivo analysis, the FvcFlw (firefly luciferase) vector was pseudotyped with VSV-G and two variant NiV pseudotypes, T234F and T234FΔN3 , as discussed above, as discussed above. 10 ng of p24 equivalents of each pseudotyped lentivirus was injected into C57/BL6 mice through the tail vein. At 5 days post-injection, luciferase expression was imaged. Following whole-body imaging (see FIG. 6), each organ was isolated to image luciferase expression (see FIG. 7). As the images demonstrate, the NiVpp pseudotyped lentivirus is able to avoid the liver sink and to effectively infect cells and deliver genetic payloads in other tissues.

[0056] In addition to the other publications cited throughout this application, the following references are incorporated herein in their entireties for all purposes: [0057] 1. An D S, Donahue R E, Kamata M, et al. Stable reduction of CCR5 by RNAi through hematopoietic stem cell transplant in non-human primates. Proc Natl Acad Sci U S A. 2007; 104:13110-13115. [0058] 2. Shimizu S, Kamata M, Kittipongdaja P, et al. Characterization of a potent non-cytotoxic shRNA directed to the HIV-1 co-receptor CCR5. Genet Vaccines Ther. 2009; 7:8. [0059] 3. Palmer A, Klein R. Multiple roles of ephrins in morphogenesis, neuronal networking, and brain function. Genes Dev. 2003; 17:1429-1450. [0060] 4. Bowden T A, Aricescu A R, Gilbert R J, Grimes J M, Jones E Y, Stuart D I. Structural basis of Nipah and Hendra virus attachment to their cell-surface receptor ephrin-B2. Nat Struct Mol Biol. 2008; 15:567-572. [0061] 5. Graf T, Stadtfeld M. Heterogeneity of embryonic and adult stem cells. Cell Stem Cell. 2008; 3:480-483. [0062] 6. Hough S R, Laslett A L, Grimmond S B, Kolle G, Pera M F. A continuum of cell states spans pluripotency and lineage commitment in human embryonic stem cells. PLoS One. 2009; 4:e7708. [0063] 7. Kullander K, Klein R. Mechanisms and functions of Eph and ephrin signalling. Nat Rev Mol Cell Biol. 2002; 3:475-486. [0064] 8. Berges B K, Akkina S R, Folkvord J M, Connick E, Akkina R. Mucosal transmission of R5 and X4 tropic HIV-1 via vaginal and rectal routes in humanized Rag2−/− gammac −/− (RAG-hu) mice. Virology. 2008; 373:342-351. [0065] 9. Damoiseaux R, Sherman S P, Alva J A, Peterson C, Pyle A D. Integrated chemical genomics reveals modifiers of survival in human embryonic stem cells. Stem Cells. 2009; 27:533-542. [0066] 10. Pyle A D, Lock L F, Donovan P J. Neurotrophins mediate human embryonic stem cell survival. Nat Biotechnol. 2006; 24:344-350. [0067] 11. Scehnet J S, Ley E J, Krasnoperov V, et al. The role of Ephs, Ephrins, and growth factors in Kaposi sarcoma and implications of EphrinB2 blockade. Blood. 2009; 113:254-263. [0068] 12. Fortunel N O, Otu H H, Ng H H, et al. Comment on “‘Stemness’: transcriptional profiling of embryonic and adult stem cells” and “a stem cell molecular signature”.

[0069] Science. 2003; 302:393; author reply 393. [0070] 13. Levroney E L, Aguilar H C, Fulcher J A, et al. Novel innate immune functions for galectin-1: galectin-1 inhibits cell fusion by Nipah virus envelope glycoproteins and augments dendritic cell secretion of proinflammatory cytokines. J Immunol. 2005; 175:413-420. [0071] 14. Arvanitis D, Davy A. Eph/ephrin signaling: networks. Genes Dev. 2008; 22:416-429. [0072] 15. Ng E S, Davis R P, Azzola L, Stanley E G, Elefanty A G. Forced aggregation of defined numbers of human embryonic stem cells into embryoid bodies fosters robust, reproducible hematopoietic differentiation. Blood. 2005; 106:1601-1603.