Adenovirus serotype 26 and serotype 35 filovirus vaccines

Abstract

Provided are recombinant adenovirus vectors (serotype 26 and serotype 35) encoding filovirus antigens. The adenovirus vectors can be used to induce protective immune responses against filovirus infection.

Claims

1. A method of inducing a protective immune response against Ebola in a subject, the method comprising: administering to the subject, as a priming vaccination, an immunologically effective amount of a recombinant adenovirus vector comprising a polynucleotide encoding a first filovirus antigenic protein, wherein the recombinant adenovirus vector is an rAd26 vector; followed by administering a boosting vaccination to the subject that includes an adenovirus vector comprising a polynucleotide encoding a second filovirus antigenic protein, wherein the adenovirus vector is an rAd35 vector, so as to induce durable T-cell memory in the subject for the first and second filovirus antigenic proteins and thus immunizing the subject against Ebola, wherein each of the first and second filovirus antigenic proteins is a glycoprotein from an Ebola virus; and wherein, three weeks following the boosting vaccination, the subject has an anti-Ebola glycoprotein EC90 antibody titer of at least 1:32,000.

2. The method according to claim 1, wherein administration is conducted intramuscularly.

3. The method according to claim 1, wherein the Ebola virus is of species Zaire.

4. The method according to claim 3, wherein the first and second filovirus antigenic proteins are encoded by SEQ ID NO: 1.

5. The method according to claim 1, wherein the Ebola virus is of species Sudan/Gulu.

6. The method according to claim 5, wherein a filovirus antigenic protein is encoded by SEQ ID NO: 2.

7. The method according to claim 5, wherein a filovirus antigenic protein is encoded by SEQ ID NO: 3.

8. A method of inducing immune response protective against death due to infection by Ebola in a subject, the method comprising: administering to the subject, as a priming vaccination, an immunologically effective amount of a recombinant adenovirus vector comprising a polynucleotide encoding a first antigenic protein encoded by a nucleic acid molecule selected from the group consisting of SEQ ID NO:1, SEQ ID NO: 2, and SEQ ID NO:3, wherein the recombinant adenovirus vector comprises an adenovirus 26 capsid protein; followed by administering a boosting vaccination to the subject, which includes an adenovirus vector comprising a polynucleotide encoding a second antigenic protein encoded by a nucleic acid molecule selected from the group consisting of SEQ ID NO:1, SEQ ID NO: 2, and SEQ ID NO:3, wherein the adenovirus vector comprises an adenovirus 35 capsid protein.

9. The method according to claim 8, wherein the first and second antigenic proteins are encoded by SEQ ID NO: 1.

10. A method of inducing an immune response protective against death due to infection by Ebola in a subject, the method comprising: administering to the subject a priming vaccination comprising an E1/E3-deleted rAd26 vector with an Ad5 E4orf6 sequence, the rAd26 vector comprising a polynucleotide encoding a first filovirus antigenic protein; and then administering to the subject a boosting vaccination comprising an E1/E3-deleted rAd35 vector with an Ad5 E4orf6 sequence, the rAd35 vector comprising a polynucleotide encoding a second filovirus antigenic protein; so as to induce durable T-cell memory in the subject for the first and second filovirus antigenic proteins and thus protecting the subject against death due to infection by Ebola, wherein each of the first and second filovirus antigenic proteins is a glycoprotein from an Ebola virus.

11. The method according to claim 10, wherein administration is conducted intramuscularly.

12. The method according to claim 10, wherein the Ebola virus is of species Zaire.

13. The method according to claim 12, wherein the first and second filovirus antigenic proteins are encoded by SEQ ID NO: 1.

14. A method of inducing a protective immune response against Ebola in a subject, the method comprising: administering to the subject, as a priming vaccination, an immunologically effective amount of a recombinant adenovirus vector comprising a polynucleotide encoding a first filovirus antigenic protein, wherein the recombinant adenovirus vector is an rAd26 vector; followed by administering a boosting vaccination to the subject that includes an adenovirus vector comprising a polynucleotide encoding a second filovirus antigenic protein wherein the adenovirus vector is an rAd35 vector, so as to induce durable T-cell memory in the subject for the first and second filovirus antigenic proteins and thus immunizing the subject against Ebola, wherein each of the first and second filovirus antigenic proteins is a glycoprotein from an Ebola virus, and wherein at least one of the priming vaccination or the boosting vaccination comprises an adjuvant selected from the group consisting of QS-21, Detox-PC, MPL-SE, MoGM-CSF, TiterMax-G, CRL- 1005, GERBU, TERamide, PSC97B, Adjumer, PG-026, GSK-I, GcMAF, B-alethine, MPC-026, Adjuvax, CpG ODN, Betafectin, MF59, lectins, growth factors, cytokines and lymphokines, alpha-interferon, gamma interferon, platelet derived growth factor (PDGF), granulocyte-colony stimulating factor (gCSF), granulocyte macrophage colony stimulating factor (gMCSF), tumor necrosis factor (TNF), epidermal growth factor (EGF), IL-I, IL-2, IL-4, IL-6, IL-8, IL-I0, IL-12, and encoding nucleic acids of any thereof.

15. A method of inducing a protective immune response against Ebola in a subject, the method comprising: administering to the subject a priming vaccination, the priming vaccination comprising: an immunologically effective amount of a first recombinant adenovirus vector comprising a polynucleotide encoding a first filovirus antigenic protein, and a immunologically effective amount of a second recombinant adenovirus vector comprising a polynucleotide encoding a second filovirus antigen protein; wherein the first and second recombinant adenovirus vectors are rAd26 vectors; followed by administering a boosting vaccination to the subject, the boosting vaccination comprising: an immunologically effective amount of a third adenovirus vector comprising a polynucleotide encoding the first filovirus antigenic protein, and a immunologically effective amount of a fourth recombinant adenovirus vector comprsing a polynucleotide encoding the second filovirus antigen protein wherein the third and fourth adenovirus vectors are rAd35 vectors, so as to induce durable T-cell memory in the subject for the first and second filovirus antigenic proteins and thus immunizing the subject against Ebola, wherein the first and second filovirus antigenic proteins are glycoproteins from different species of Ebola virus.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1. Adenovirus genetic grouping and vector organization. (A) Phylogenetic tree showing the relationship of the adenovirus hexon sequences. The different subgroups A until F are indicated and human adenovirus serotypes 26 and 35 are highlighted. The tree was constructed using the neighbor-joining method of the ClustalX package (Larkin et al., 2007) and drawn using the Phylip Phylogeny Inference package version 3.68. Confidence values are displayed at internal branches as a percent of 1000 times bootstrap. (B) Schematic overview of the genome of recombinant Ad26 and recombinant Ad35 vectors. Both vectors have a full deletion of E1 and contain an expression cassette containing the EBOV glycoprotein gene under control of the CMV promoter. Further deletions were made in the E3 regions and the respective E4 orf6 sequences were replaced by the Ad5 E4orf6 sequences to facilitate the replication of these vaccine vectors on Ad5 E1 complementing cell lines like PER.C6 cells.

(2) FIG. 2. rAd35-GP (using Ad35BSU.Ebo.GP(Z)FL.wt) vaccine-induced immune responses and EBOV challenge. (A) The quantity of anti-EBOV GP IgG in plasma samples obtained 3 weeks after vaccination from Ad5-nave (gray bars) and Ad5-immune (black bars), rAd35-GP vaccinated cynomolgus macaques determined by ELISA. EC90 antibody titers were determined as described in Methods. (B, C) Frequency of antigen-specific CD4.sup.+ and CD8.sup.+ T-lymphocyte responses enumerated in the memory cell subsets by ICS for IL-2 (CD4) or TNF- (CD8), and analysis by flow cytometry after stimulation of week 3 post-vaccine PBMC. (D) Plasma AST liver enzyme levels in rAd35-GP vaccinated (blue, Ad5-nave; red, Ad5-immune) and control (black) macaques after infectious challenge with 1000 PFU ZEBOV.

(3) FIG. 3. Dose response for rAd35-GP induction of immune responses in macaques (using Ad35BSU.Ebo.GP(Z)FL.wt and Ad35BSU.Ebo.GP(S/G)FL). (A) GP-specific ELISA IgG antibody titers (EC90) in plasma obtained from macaques 3 weeks after vaccination with 10.sup.10 or 10.sup.11 virus particles of each of the rAd35-GP vectors (Ad35BSU.Ebo.GP(Z)FL.wt and Ad35BSU.Ebo.GP(S/G)FL). (B, C) Antigen-specific CD4.sup.+ and CD8.sup.+ T cell frequencies assessed by ICS as in FIG. 2. Gray bars, 10.sup.10 virus particles rAd35-GP; black bars, 10.sup.11 virus particles rAd35-GP. (D, E) Plasma AST liver enzyme levels following challenge with 1000 PFU ZEBOV. Blue, 10.sup.10 virus particles of rAd35-GP; red, 10.sup.11 virus particles rAd35-GP and black, control.

(4) FIG. 4. Ability of rAd26-GP vectors to induce antigen-specific antibody and T-lymphocyte responses in cynomolgus macaques (using Ad26.Ebo.GP(Z)FL.wt and Ad26.Ebo.GP(S/G)FL.wt). (A) ELISA IgG antibody titers (EC90), and (B, C) frequencies of GP-specific CD4.sup.+ and CD8.sup.+ T cells, (D) Plasma AST liver enzymes are shown for individual cynomolgus macaques in two separate studies. Study 1 subjects received a vaccine dose of either 10.sup.10 or 10.sup.11 rAd26 virus particles of each of the rAd26-GP vectors (Ad26.Ebo.GP(Z)FL.wt and Ad26.Ebo.GP(S/G)FL.wt) and Study 2 subjects received a dose of 10.sup.12 virus particles of each of the rAd26-GP vectors (Ad26.Ebo.GP(Z)FL.wt and Ad26.Ebo.GP(S/G)FL.wt).

(5) FIG. 5. Kaplan-Meier survival curves for rAd26-GP vaccinated macaques (using Ad26.Ebo.GP(Z)FL.wt and Ad26.Ebo.GP(S/G)FL.wt). Unvaccinated control and animals vaccinated with rAd26-GP were infected four weeks after vaccination with 1000 PFU ZEBOV in two separate challenge experiments as shown in FIG. 4. Panel A: Black lines show unvaccinated subjects and dark blue lines show Ad26-vaccinated subjects at doses indicated. Panel B: one group of rAd35-vaccinated subjects (light blue) is shown for potency comparison with Ad26 at a dose of 10.sup.11 virus particles of each the rAd26-GP vectors (Ad26.Ebo.GP(Z)FL.wt and Ad26.Ebo.GP(S/G)FL.wt). Panel C: Historical Ad5-vaccinated macaque survival (red) compared to subjects vaccinated with 10.sup.12 virus particles of each the rAd26-GP vectors (Ad26.Ebo.GP(Z)FL.wt and Ad26.Ebo.GP(S/G)FL.wt).

(6) FIG. 6. Comparison of prime and boost immune responses after rAd26-GP/rAd35-GP vaccinations (using Ad26.Ebo.GP(Z)FL.wt and Ad26.Ebo.GP(S/G)FL.wt followed by Ad35BSU.Ebo.GP(Z)FL.wt and Ad35BSU.Ebo.GP(S/G)FL). (A) The quantity of anti-EBOV GP IgG in plasma samples obtained 3 weeks after vaccination from Ad5-nave (gray bars) and Ad5-immune (black bars), rAd35-GP vaccinated cynomolgus macaques determined by ELISA. EC90 antibody titers were determined as described in Methods. (B, C) Frequency of antigen-specific CD4.sup.+ and CD8.sup.+ T-lymphocyte responses enumerated in the memory cell subsets by ICS for IL-2 (CD4) or TNF- (CD8), and analysis by flow cytometry after stimulation of week 3 post-vaccine PBMC. (D, E) EBOV challenge results. Plasma AST liver enzyme levels (D), and Kaplan-Meier survival curve (E) for rAd26-GP/rAd35-GP vaccinated macaques after infectious challenge with 1000 PFU ZEBOV (blue, rAd26-GP/rAd35-GP; red, Ad5-GP and black, unvaccinated control).

DETAILED DESCRIPTION

(7) The disclosure is based upon, at least in part, the finding that rAd35 and rAd26 vectors upon single inoculation as well as heterologous prime-boost combinations generate protective immune responses against filovirus infection. In particular, the disclosure provides evidence that heterologous prime-boost combinations (in particular, Ad26 prime followed by Ad35 boost) are surprisingly effective in generating protective immune responses. The surprising effectiveness of these prime-boost combinations could not have been predicted at the time hereof. Thus, the disclosure provides recombinant adenoviral vectors (rAd35 or rAd26) that express filovirus antigens. The adenoviral vectors can be formulated as vaccines and used to induce protective immunity against filovirus infections either alone or in prime-boost combinations.

(8) Filovirus Antigens

(9) The Ebola viruses, and the genetically-related Marburg virus, are filoviruses associated with outbreaks of highly lethal hemorrhagic fever in humans and primates in North America, Europe, and Africa (Peters, C. J. et al., in: Fields Virology, eds. Fields, B. N. et al., 1161-1176, Philadelphia, Lippincott-Raven, 1996; Peters, C. J. et al., 1994 Semin Virol 5:147-154). Although several subtypes have been defined, the genetic organization of these viruses is similar, each containing seven linearly arrayed genes. Among the viral proteins, the envelope glycoprotein exists in two alternative forms, a 50-70 kilodalton (kDa) secreted protein (sGP) and a 130 kDa transmembrane glycoprotein (GP) generated by RNA editing that mediates viral entry (Peters, C. J. et al., in: Fields Virology, eds. Fields, B. N. et al., 1161-1176, Philadelphia, Lippincott-Raven, 1996; Sanchez, A. et al., 1996 PNAS USA 93:3602-3607). Other structural gene products include the nucleoprotein (NP), matrix proteins VP24 and VP40, presumed nonstructural proteins VP30 and VP35, and the viral polymerase (reviewed in Peters, C. J. et al., in: Fields Virology, eds. Fields, B. N. et al., 1161-1176, Philadelphia, Lippincott-Raven, 1996).

(10) The nucleic acid molecules may encode structural gene products of any filovirus species. There are five species of Ebola viruses, Zaire (type species, also referred to herein as ZEBOV), Sudan (also referred to herein as SEBOV), Reston, Bundibugyo, and Ivory Coast. There is a single species of Marburg virus (also referred to herein as MARV).

(11) The particular antigen expressed in the vectors hereof is not a critical aspect of the disclosure. The adenoviral vectors hereof can be used to express proteins comprising an antigenic determinant of a wide variety of filovirus antigens. In a typical and preferred embodiment, the vectors hereof include nucleic acid encoding the transmembrane form of the viral glycoprotein (GP). In other embodiments, the vectors hereof may encode the secreted form of the viral glycoprotein (SGP), or the viral nucleoprotein (NP).

(12) One of skill will recognize that the nucleic acid molecules encoding the filovirus antigenic protein may be modified, e.g., the nucleic acid molecules set forth herein may be mutated, as long as the modified expressed protein elicits an immune response against a pathogen or disease. Thus, as used herein, the term filovirus antigenic protein refers to a protein that comprises at least one antigenic determinant of a filovirus protein described above. The term encompasses filovirus antigens (i.e., gene products of a filovirus), as well as recombinant proteins that comprise one or more filovirus antigenic determinants.

(13) In some embodiments, the protein may be mutated so that it is less toxic to cells (see e.g., WO/2006/037038). The disclosure also includes vaccines comprising a combination of nucleic acid molecules. For example, and without limitation, nucleic acid molecules encoding GP, SGP and NP of the Zaire, Sudan and Ivory Coast Ebola strains may be combined in any combination, in one vaccine composition.

(14) Adenoviral Vectors

(15) As noted above, exposure to certain adenoviruses has resulted in immune responses against certain adenoviral serotypes, which can affect efficacy of adenoviral vaccines. The disclosure provides adenoviral vectors comprising capsid proteins from two rare serotypes: Ad26 and Ad35. In the typical embodiment, the vector is an rAd26 or rAd35 virus.

(16) Thus, the vectors hereof comprise an Ad26 or Ad35 capsid protein (e.g., a fiber, penton or hexon protein). One of skill will recognize that it is not necessary that an entire Ad26 or Ad35 capsid protein be used in the vectors hereof. Thus, chimeric capsid proteins that include at least a part of an Ad26 or Ad35 capsid protein can be used in the vectors hereof. The vectors hereof may also comprise capsid proteins in which the fiber, penton, and hexon proteins are each derived from a different serotype, so long as at least one capsid protein is derived from Ad26 or Ad35. In preferred embodiments, the fiber, penton and hexon proteins are each derived from Ad26 or each from Ad35.

(17) One of skill will recognize that elements derived from multiple serotypes can be combined in a single recombinant adenovirus vector. Thus, a chimeric adenovirus that combines desirable properties from different serotypes can be produced. Thus, in some embodiments, a chimeric adenovirus hereof could combine the absence of pre-existing immunity of the Ad26 and Ad35 serotypes with characteristics, such as temperature stability, assembly, anchoring, production yield, redirected or improved infection, stability of the DNA in the target cell, and the like.

(18) In certain embodiments the recombinant adenovirus vector hereof is derived mainly or entirely from Ad35 or from Ad26 (i.e., the vector is rAd35 or rAd26). In some embodiments, the adenovirus is replication deficient, e.g., because it contains a deletion in the E1 region of the genome. For the adenoviruses hereof, being derived from Ad26 or Ad35, it is typical to exchange the E4-orf6 coding sequence of the adenovirus with the E4-orf6 of an adenovirus of human subgroup C, such as Ad5. This allows propagation of such adenoviruses in well known complementing cell lines that express the E1 genes of Ad5, such as, for example, 293 cells, PER.C6 cells, and the like (see, e.g., Havenga et al., 2006, J Gen Virol 87: 2135-43; WO 03/104467). In certain embodiments, the adenovirus is a human adenovirus of serotype 35, with a deletion in the E1 region into which the nucleic acid encoding the antigen has been cloned, and with an E4 orf6 region of Ad5. In certain embodiments, the adenovirus is a human adenovirus of serotype 26, with a deletion in the E1 region into which the nucleic acid encoding the antigen has been cloned, and with an E4 orf6 region of Ad5. For the Ad35 adenovirus, it is typical to retain the 3 end of the E1B 55K open reading frame in the adenovirus, for instance the 166 bp directly upstream of the pIX open reading frame or a fragment comprising this, such as a 243 bp fragment directly upstream of the pIX start codon, marked at the 5 end by a Bsu36I restriction site, since this increases the stability of the adenovirus because the promoter of the pIX gene is partly residing in this area (see, e.g., Havenga et al., 2006, supra; WO 2004/001032).

(19) The preparation of recombinant adenoviral vectors is well known in the art. Preparation of rAd26 vectors is described, for example, in WO 2007/104792 and in Abbink et al., (2007) Virol 81(9): 4654-63. Exemplary genome sequences of Ad26 are found in GenBank Accession EF 153474 and in SEQ ID NO:1 of WO 2007/104792. Preparation of rAd35 vectors is described, for example, in U.S. Pat. No. 7,270,811 and in Vogels et al., (2003) J Virol 77(15): 8263-71. An exemplary genome sequence of Ad35 is found in GenBank Accession AC_000019.

(20) Typically, a vector hereof is produced using a nucleic acid comprising the entire recombinant adenoviral genome (e.g., a plasmid, cosmid, or baculovirus vector). Thus, the invention also provides isolated nucleic acid molecules that encode the adenoviral vectors hereof. The nucleic acid molecules hereof may be in the form of RNA or in the form of DNA obtained by cloning or produced synthetically. The DNA may be double-stranded or single-stranded.

(21) The adenovirus vectors hereof are typically replication defective. In these embodiments, the virus is rendered replication-defective by deletion or inactivation of regions critical to replication of the virus, such as the E1 region. The regions can be substantially deleted or inactivated by, for example, inserting the gene of interest (usually linked to a promoter). In some embodiments, the vectors hereof may contain deletions in other regions, such as the E2, E3 or E4 regions or insertions of heterologous genes linked to a promoter. For E2- and/or E4-mutated adenoviruses, generally E2- and/or E4-complementing cell lines are used to generate recombinant adenoviruses. Mutations in the E3 region of the adenovirus need not be complemented by the cell line, since E3 is not required for replication.

(22) A packaging cell line is typically used to produce sufficient amount of adenovirus vectors hereof. A packaging cell is a cell that comprises those genes that have been deleted or inactivated in a replication-defective vector, thus allowing the virus to replicate in the cell. Suitable cell lines include, for example, PER.C6, 911, 293, and E1 A549.

(23) As noted above, a wide variety of filovirus antigenic proteins can be expressed in the vectors hereof. If required, the heterologous gene encoding the filovirus antigenic protein can be codon-optimized to ensure proper expression in the treated host (e.g., human). Codon-optimization is a technology widely applied in the art. Typically, the heterologous gene is cloned into the E1 and/or the E3 region of the adenoviral genome.

(24) The heterologous filovirus gene may be under the control of (i.e., operably linked to) an adenovirus-derived promoter (e.g., the Major Late Promoter) or may be under the control of a heterologous promoter. Examples of suitable heterologous promoters include the CMV promoter and the RSV promoter. Preferably, the promoter is located upstream of the heterologous gene of interest within an expression cassette.

(25) As noted above, the adenovirus vectors hereof can comprise a wide variety of filovirus antigens known to those of skill in the art. Table 1 provides a summary of exemplary vectors hereof.

(26) TABLE-US-00001 TABLE 1 VRC number of source plasmid for Sequence of Vector name insert insert Description Ad5.Ebo.GP(Z)FL.wt 6001 SEQ ID NO: 1 ZEBOV GP wild type Ad5.Ebo.GP(S/G)FL.wt 6610 SEQ ID NO: 3 SEBOV GP wild type Ad5.Mar.GP(A)FL 6712 SEQ ID NO: 4 MARV Angola codon optimized Ad26.Ebo.GP(Z)FL.wt 6001 SEQ ID NO: 1 ZEBOV GP wild type Ad26.Ebo.GP(S/G)FL.wt 6610 SEQ ID NO: 3 SEBOV GP wild type Ad26.Mar.GP(A)FL 6712 SEQ ID NO: 4 MARV Angola codon optimized Ad35BSU.Ebo.GP(Z)FL.wt 6001 SEQ ID NO: 1 ZEBOV GP wild type Ad35BSU.Ebo.GP(S/G)FL 6611 SEQ ID NO: 2 SEBOV GP codon optimized Ad35BSU.Mar.GP(A)FL 6712 SEQ ID NO: 4 MARV Angola codon optimized
Immunogenic Compositions

(27) Purified or partially purified adenovirus vectors hereof may be formulated as a vaccine (also referred to as an immunogenic composition) according to methods well known in the art. Such compositions may include adjuvants to enhance immune responses. The optimal ratios of each component in the formulation may be determined by techniques well known to those skilled in the art.

(28) The preparation and use of immunogenic compositions are well known to those of skill in the art. Liquid pharmaceutical compositions generally include a liquid carrier, such as water, petroleum, animal or vegetable oils, mineral oil or synthetic oil. Physiological saline solution, dextrose or other saccharide solution or glycols, such as ethylene glycol, propylene glycol or polyethylene glycol may be included.

(29) The compositions are suitable for single administrations or a series of administrations. When given as a series, inoculations subsequent to the initial (priming) administration are given to boost the immune response and are typically referred to as booster inoculations. The compositions hereof can be used as a boosting composition primed by antigen using any of a variety of different priming compositions, or as the priming composition. Thus, one aspect of the disclosure provides a method of priming and/or boosting an immune response to an antigen in an individual. For example, in some preferred embodiments, a priming administration of one adenoviral vector hereof (e.g., rAd26) is followed by a booster inoculation of the second adenoviral vector (e.g., rAd35).

(30) The timing of the administration of boosting compositions is well within the skill in the art. Boosting composition are generally administered weeks or months after administration of the priming composition, for example, about 2-3 weeks or 4 weeks, or 8 weeks, or 16 weeks, or 20 weeks, or 24 weeks, or 28 weeks, or 32 weeks or one to two years.

(31) The compositions hereof may comprise other filovirus antigens or the priming or boosting inoculations may comprise other antigens. The other antigens used in combination with the adenovirus vectors hereof are not critical to the invention and may be, for example, filovirus antigens, nucleic acids expressing them, virus like particles (VLPs), or prior art viral vectors. Such viral vectors include, for example, other adenoviral vectors, vaccinia virus vectors, avipox vectors, such as fowlpox or canarypox, herpes virus vectors, a vesicular stomatitis virus vectors, or alphavirus vectors. One of skill will recognize that the immunogenic compositions hereof may comprise multiple antigens and vectors.

(32) The antigens in the respective priming and boosting compositions (however many boosting compositions are employed) need not be identical, but should share antigenic determinants.

(33) As noted above, the immunogenic compositions hereof may comprise adjuvants. Adjuvants suitable for co-administration in accordance with the disclosure should be ones that are potentially safe, well tolerated and effective in people including QS-21, Detox-PC, MPL-SE, MoGM-CSF, TiterMax-G, CRL-1005, GERBU, TERamide, PSC97B, Adjumer, PG-026, GSK-I, GcMAF, B-alethine, MPC-026, Adjuvax, CpG ODN, Betafectin, Alum, and MF59.

(34) Other adjuvants that may be administered include lectins, growth factors, cytokines and lymphokines, such as alpha-interferon, gamma interferon, platelet derived growth factor (PDGF), granulocyte-colony stimulating factor (gCSF), granulocyte macrophage colony stimulating factor (gMCSF), tumor necrosis factor (TNF), epidermal growth factor (EGF), IL-I, IL-2, IL-4, IL-6, IL-8, IL-IO, and IL-12 or encoding nucleic acids therefore.

(35) As noted above, the compositions hereof may comprise a pharmaceutically acceptable excipient, carrier, buffer, stabilizer or other materials well known to those skilled in the art. Such materials should be non-toxic and should not interfere with the efficacy of the active ingredient. The precise nature of the carrier or other material may depend on the route of administration, e.g., oral, intravenous, cutaneous or subcutaneous, intramucosal (e.g., gut), intranasal, intramuscular, or intraperitoneal routes. Administration is typically intramuscular.

(36) Intramuscular administration of the immunogenic compositions may be achieved by using a needle to inject a suspension of the adenovirus vector. An alternative is the use of a needless injection device to administer the composition (using, e.g., BIOJECTOR) or a freeze-dried powder containing the vaccine.

(37) For intravenous, cutaneous or subcutaneous injection, or injection at the site of affliction, the adenovirus vector will be in the foam of a parenterally acceptable aqueous solution which is pyrogen-free and has suitable pH, isotonicity and stability. Those of skill in the art are well able to prepare suitable solutions using, for example, isotonic vehicles, such as Sodium Chloride Injection, Ringer's Injection, and Lactated Ringer's Injection. Preservatives, stabilizers, buffers, antioxidants and/or other additives may be included, as required. A slow-release formulation may also be employed.

(38) Typically, administration will have a prophylactic aim to generate an immune response against a filovirus antigen before infection or development of symptoms. Diseases and disorders that may be treated or prevented in accordance with the disclosure include those in which an immune response may play a protective or therapeutic role. In other embodiments, the adenovirus vectors can be administered for post-exposure prophylactics.

(39) The immunogenic compositions containing the adenovirus vectors are administered to a subject, giving rise to an anti-filovirus immune response in the subject. An amount of a composition sufficient to in induce a detectable immune response is defined to be an immunologically effective dose. As shown below, the immunogenic compositions hereof induce a humoral as well as a cell-mediated immune response. In a typical embodiment the immune response is a protective immune response.

(40) The actual amount administered, and rate and time-course of administration, will depend on the nature and severity of what is being treated. Prescription of treatment, e.g., decisions on dosage etc., is within the responsibility of general practitioners and other medical doctors, or in a veterinary context a veterinarian, and typically takes account of the disorder to be treated, the condition of the individual patient, the site of delivery, the method of administration and other factors known to practitioners. Examples of the techniques and protocols mentioned above can be found in Remington's Pharmaceutical Sciences, 16th edition, Osol, A. ed., 1980.

(41) Following production of adenovirus vectors and optional formulation of such particles into compositions, the adenovirus vectors may be administered to an individual, particularly human or other primate. Administration may be to humans, or another mammal, e.g., mouse, rat, hamster, guinea pig, rabbit, sheep, goat, pig, horse, cow, donkey, monkey, dog or cat. Delivery to a non-human mammal need not be for a therapeutic purpose, but may be for use in an experimental context, for instance in investigation of mechanisms of immune responses to the adenovirus vector.

(42) In one exemplary regimen, the adenovirus vector is administered (e.g., intramuscularly) in the range of from about 100 l to about 10 ml of saline solution containing concentrations of from about 10.sup.4 to 10.sup.12 virus particles/ml. Typically, the adenovirus vector is administered in an amount of about 10.sup.9 to about 10.sup.12 viral particles (vp) to a human subject during one administration, more typically from about 10.sup.10 to about 10.sup.12 vp. An initial vaccination can be followed by a boost as described above. The composition may, if desired, be presented in a kit, pack or dispenser, which may contain one or more unit dosage forms containing the active ingredient. The kit, for example, may comprise metal or plastic foil, such as a blister pack. The kit, pack, or dispenser may be accompanied by instructions for administration.

(43) The compositions hereof may be administered alone or in combination with other treatments, either simultaneously or sequentially dependent upon the condition to be treated.

EXAMPLES

(44) The following examples are offered to illustrate, but not to limit the claimed invention.

(45) There are distinct advantages associated with either single-shot or prime-boost immunization depending on the need for immediate versus long-term immunity must be taken into account when optimizing immunization regimens. EBOV and other filovirus outbreaks tend to occur suddenly and spread quickly among populations in which medical facilities are scarce. Thus, under these circumstances, short vaccine regimens may be desirable. For this reason, single-shot vaccinations with rAd5 vectors containing EBOV glycoprotein (GP) and nucleoprotein (NP) genes have been developed in non-human primates (Sullivan, et al., 2006). Such vaccines have been shown to elicit strong immune responses within one month (Sullivan, et al., 2003), probably due to high expression levels of the inserts and the tropism of Ad5 for dendritic cells. On the other hand, long-term protective immunity will likely require a prime-boost vaccine regimen comprising two or more administrations that can induce durable T-cell memory. Therefore, we designed a series of experiments to test immunogenicity and potency for both single inoculation and a prime-boost combinations using rAd35 and rAd26 vectors, and the results of these studies are presented herein.

(46) Materials and Methods

(47) Generation rAd Ebola vaccines. Low seroprevalent E1/E3-deleted rAd26 and rAd35 vaccine vectors expressing EBOV GPs were constructed, grown and purified as described previously (Abbink, et al., 2007). An Ad5 vector, not expressing EBOV GP, was constructed, grown and purified by the same method and used to induce immunity to Ad5 in selected animals as indicated in each experiment. EBOV GP inserts spanning the open reading frames of Zaire (SEQ ID NO:1) and Sudan/Gulu (SEQ ID NO:2) species were cloned under transcriptional control of the human CMV promoter and the SV-40 polyadenylation sequence into a plasmid containing the left portion of the Ad genome, including left ITR and packaging signal. Co-transfection of this plasmid with a cosmid containing the remaining Ad sequence (E3-deleted) to PER.C6 cells yielded an E1/E3-deleted replication deficient recombinant Ad26 or Ad35 vaccine vector. To facilitate replication of rAd26 and rAd35 vectors on PER.C6 cells, the native E4 orf6 regions were replaced by the Ad5 E4orf6 sequence (Havenga, et al., 2006). The rAd viruses were plaque purified and one plaque of each was expanded up to a production scale of approximately 2.4 L. A two step cesium chloride gradient ultracentrifugation procedure was used to purify the rAd EBOV vectors. The purified rAd EBOV vaccines were stored as single use aliquots below 65 C. Virus particle titers were determined measuring the optical density at 260 nm (Maizel, et al., 1968 Virology 36(1): 115-25). Infectivity was assessed by TCID50 using 911 cells (Fallaux, et al., (1996) Hum Gene Ther 7(2): 215-22). Adenovirus-mediated EBOV GP expression was assessed by infection of A549 cells followed by analysis of culture lysates on Western blot. The identity of the purified vectors was confirmed by PCR and the complete transgene regions, including flanking sequences were checked using DNA sequencing.

(48) Phylogenetic Analysis. The phylogenetic tree was constructed using full length adenovirus hexon amino acid sequences. Amino acid sequences were aligned using the Clustal X programme (Larkin, et al., (2007) Bioinformatics 23(21): 2947-8) and the tree was built using the Clustal X Neighbour-Joining method and the tree was bootstrapped 1000 times. The tree was visualized and plotted using the Drawtree programme from the Phylip Phylogeny Inference package version 3.68.

(49) Animal Challenge Study and Safety. Animal experiments were conducted in full compliance with all relevant federal guidelines and NIH policies. Cynomolgus macaques (Macaca fascicularis) 3-5 years of age and weighing between 2-3 kg were obtained from Covance for all studies. Monkeys were housed individually and given enrichment regularly as recommended by the Guide for the Care and Use of Laboratory Animals (DHEW number NIH 86-23). Animals were anesthetized with ketamine prior to blood sampling or vaccination. Each vaccine group in this study contained three cynomolgus macaques, and each control group contained a single cynomolgus macaque. Four weeks post EBOV vaccination, animals were transferred to the Maximum Containment Laboratory (BSL-4) for infection with a target dose of 1,000 PFU of Zaire EBOV delivered by the intramuscular route into the caudal thigh. The ZEBOV challenge stock was prepared from a human fatality in the 1995 outbreak in the former Zaire. Animals remained there until the completion of the study. While in the BSL-4 facility the monkeys were fed and checked at a minimum of once daily.

(50) Animal studies performed in BSL-4 biocontainment at USAMRIID were approved by the USAMRIID Institutional Animal Care and Use Committee. Animal research was conducted in compliance with the Animal Welfare Act and other Federal statutes and regulations relating to animals and experiments involving animals and adheres to the principles stated in the Guide for the Care and Use of Laboratory Animals, National Research Council, 1996. The facilities used are fully accredited by the Association for Assessment and Accreditation of Laboratory Animal Care International.

(51) Animal Immunization. Subjects received intramuscular vaccinations in the bi-lateral deltoids by needle and syringe with doses and vectors indicated in each experiment. Selected animals, as indicated in each experiment, were pre-immunized with 10.sup.11 PFU of an empty Ad5 vector to induce Ad5 immunity. Ad5 ELISA antibody titers were established in these animals prior to EBOV vaccination.

(52) Anti-EBOV GP IgG ELISA. Polyvinyl chloride ELISA plates (Dynatech, Vienna, Va., or Nunc, Rochester, N.Y.) were coated with 100 l of antigen per well and incubated at 4 C. overnight. Subsequent incubations were performed at room temperature. Transmembrane-deleted EBOV GP (EBOV GPTM) generated by calcium phosphate-mediated transient transfection of 293T cells served as the antigen. Plates were washed six times with PBS containing Tween 20 after antigen coating. Test sera were serially diluted to 7 concentrations ranging from 1:50 to 1:50,000 and added to the antigen-coated wells for 60 minutes. The plates were washed six times followed by incubation with detection antibody, goat anti-human IgG (H+L; Chemicon/Millipore, Billerica, Mass.) conjugated to horseradish peroxide. Sigma Fast o-Phenylenediamine Dihydrochloride (Sigma, St. Louis, Mo.) substrate was added to the wells and the optical density was determined (450 nm). A prevaccination serum sample for each animal was run every time the assay was performed. A positive control serum sample from a single animal with a known Zaire EBOV GP IgG response was run every time the assay was performed. Background-subtracted ELISA titers are expressed as EC90, reciprocal optical density values, which represent the dilution at which there is a 90% decrease in antigen binding.

(53) Intracellular Cytokine Staining. Whole blood samples from cynomolgus macaques were subjected to density gradient centrifugation over Ficoll to isolate peripheral blood mononuclear cells (PBMC). Approximately 110.sup.6 cells were stimulated in 100 l RPMI medium containing 10% heat inactivated fetal calf serum for 6 hours at 37 C. with anti-CD28 (clone CD28.2) and -CD49d (clone L25) antibodies (BD Biosciences), Brefeldin-A (Sigma-Aldrich, St. Louis, Mo.), and either DMSO or a pool of peptides spanning the entire Zaire EBOV GP open reading frame. The peptides were 15-mers overlapping by 11 amino acids reconstituted in fresh sterile DMSO at a final concentration of 2.5 g/ml for each peptide. For each sample equivalent an aliquot was stimulated with SEB as a positive control. After the six hour stimulation, PBMC were stained with a mixture of antibodies against lineage markers (CD3-Cy7-APC, clone SP34-2 (BD Biosciences), CD4-QD605 clone M-T477 (BD Biosciences), CD8-TRPE clone RPA-T8, CD95 Cy5-PE, clone DX2 (BD Biosciences), CD45RA QD655, clone 5H3, at room temperature for 20 min. The CD45RA QD655 and CD8-TRPE antibodies were conjugated according to standardized protocols as previously described (Koup et al., 2010 Priming Immunization with DNA Augments Immunogenicity of Recombinant Adenoviral Vectors for Both HIV-1 Specific Antibody and T-Cell Responses. PLoS One 5(2): e9015. doi:10.1371/journal.pone.0009015). After 2 washes the cells were fixed and permeabilized with Cytofix/Cytoperm (BD Biosciences) followed by staining with antibodies against cytokines TNF-APC, clone MAb11 (BD Biosciences), and IL-2 PE, clone MQ17H12 (BD Biosciences). The viability dye ViViD (Invitrogen) was included to allow discrimination between live and dead cells (Perfetto, et al., (2006) J Immunol Methods 313(1-2): 199-208). Samples were acquired on an LSR II cytometer (BD Biosciences), collecting up to 1,000,000 events and analyzed using FlowJo 9.1 and SPICE 5.0 software (Tree Star). Cytokine positive cells were defined as a percentage within CD4.sup.+ and CD8.sup.+ T cell memory subsets. Memory subsets were defined as CD45RA/CD95+ or CD28/CD95+. In the later case, CD28 Alexa488 (clone 28.2, BioLegend) was used for stimulation instead of unconjugated CD28 mAb.

(54) Serum Biochemistry. For challenge studies, blood was collected from the NHP on days 0, 3, 6, 10, 14 and 28 post Zaire EBOV infection. Total white blood cell counts, white blood cell differentials, red blood cell counts, platelet counts, hematocrit values, total hemoglobin, mean cell volume, mean corpuscular volume, and mean corpuscular hemoglobin concentration were determined from blood samples collected in tubes containing EDTA, by using a laser-based hematologic Analyzer (Coulter Electronics, Hialeah, Fla., USA). Serum samples were tested for concentrations of aspartate aminotransferase (AST), by using a Piccolo Point-Of-Care Blood Analyzer (Abaxis, Sunnyvale, Calif., USA).

(55) Detection of EBOV. Virus titration was performed by plaque assay on Vero cells. Briefly, increasing 10-fold dilutions of plasma samples were adsorbed to Vero monolayers in duplicate wells (0.2 ml per well); thus, the limit for detection was 25 pfu/ml.

(56) Statistics. Comparison of anti-GP ELISA IgG titers, and intracellular cytokine production by T cells memory subsets was done using a two-tailed T test in GraphPad Prism software.

(57) Results

(58) Adenovirus Phylogeny and Vector Construction. rAd5 genetic vaccines for EBOV provide potent protective immunity in macaques, and have been proven safe and immunogenic in human clinical trials (Asmuth, et al.; Kibuuka, et al.; Harro, et al., 2009;). Studies in macaques and humans have shown that-pre-existing vector directed immunity can limit the potency of viral vector-based vaccines (McCoy, et al., 2007; Buchbinder, et al., 2008). Since seroprevalence data suggest that a large proportion of humans worldwide have experienced natural infection with Ad5we evaluated other adenovirus serotypes for use as vaccine vectors (FIG. 1A). Ad35, a group B and Ad26, a group D adenovirus segregate genetically from rAd5, Group C, so we hypothesized that vaccine vectors derived from these serotypes will be less sensitive to Ad5 immunity in primates. Although Ad35 and Ad26 vectors use receptors distinct from Ad5 usage, they nonetheless demonstrate efficient transduction of monocyte-derived dendritic cells, and circumvent Ad5 immunity in mice. Therefore, GP inserts from the Zaire or Sudan/Gulu species of EBOV were cloned under transcriptional control of the human CMV promoter into the E1 region of rAd35 and rAd26 vectors (FIG. 1B). Both vector genomes have been deleted in the E1 genes in order to render them replication deficient and reduce the potential for recombination in vaccinated subjects.

(59) rAd35 vaccination and induction of immune responses in macaques. Initial studies were conducted with a single EBOV species-vaccine encoding the GP from ZaireEbolavirus (ZEBOV), GP(Z), to test the ability of rAd35 vectors to induce immune responses in Ad5 nave macaques, and also to evaluate vector potency within the context of pre-existing immunity to Ad5. Six cynomolgus macaques, three Ad5-nave and three Ad5-immune, were each vaccinated intramuscularly with 10.sup.10 particles of rAd35-GP(Z) (Ad35BSU.Ebo.GP(Z)FL.wt) by needle injection. At three weeks post-vaccination, antigen-specific antibody and T-cell responses were evaluated in peripheral blood samples obtained from individual subjects. Antibodies against EBOV-GP(Z) assessed by ELISA were induced in all subjects, demonstrating that rAd35-GP(Z) vectors mediated successful in vivo transduction of target cells and efficient antigen presentation (FIG. 2A). Ad5-nave and Ad5-immune subjects generated serum antibody titers ranging from approximately 1:700 to 1:3000. These antibody levels are in the range that has been observed for Ad5-based vaccines containing GP(Z) inserts and exceed the minimum value (1:500) that has been associated with immune protection against EBOV infection in this macaque-Ad vaccine model (Sullivan, 2009). Although significant antibody titers were induced in all vaccinees, none of the subjects exceeded the threshold titer (ca. 1:3500) that predicts 100% protection following administration of Ad5-GP vaccine vectors in macaques. It is noteworthy, however, that comparison of antibody titers in Ad5-nave versus Ad5-immune subjects showed that there was no significant difference in average titers elicited among these groups (1:1600 vs 1:1800 respectively), suggesting that rAd35 vectors are effective vaccines in subjects who have been exposed previously to Ad5.

(60) Cellular immune responses were evaluated by intracellular cytokine staining (ICS) for either TNF- (CD8.sup.+) or IL-2 (CD4.sup.+) after stimulation of subject PBMC with overlapping peptides spanning the EBOV GP(Z) open reading frame. Surface staining of lymphocytes using CD45RA and CD95 was performed to assess antigen-specific immune responses in the memory subpopulations of CD4.sup.+ and CD8.sup.+ T-cells (FIGS. 2B and 2C). As observed for antibody responses, macaques vaccinated with the rAd35 vector generated cellular immunity against EBOV-GP, and the frequency of antigen-specific T-cells was not affected by Ad5 immune status. The rank order magnitude of cellular responses in both CD4.sup.+ and CD8.sup.+ lymphocytes across subjects was similar to antibody responses, although the frequency of antigen-specific T-cells for one subject V3 was below detectable levels. Previous studies in macaques have shown that rAd5-based vaccine vectors induce CD8.sup.+ T cell frequencies that are dominant over CD4.sup.+ responses. In the present study, rAd35-vaccinated subjects generated GP-specific CD4.sup.+ and CD8.sup.+ lymphocyte at similar frequencies. However, given the relatively small number of subjects tested, it is possible that differences, if present, could not be revealed. All-together these results demonstrate that rAd35-GP is immunogenic in cynomolgus macaques and that vector potency for the induction of antigen-specific humoral and cell-mediated immune responses is not reduced in subjects with pre-existing immunity to Ad5.

(61) Challenge of rAd35-Vaccinated Macaques with ZEBOV. We next tested whether vaccination with rAd35-GP provides protection against infectious challenge with a high dose of ZEBOV. One week after the assessment of immune responses shown above, the six rAd35-GP vaccinated and one nave cynomolgus macaque were exposed to 1000 PFU of the 1995 Kikwit strain of ZEBOV by intramuscular injection. Hepatic enzymes were measured regularly after infectious challenge since elevations in these markers are characteristic of productive EBOV infection in macaques. Circulating levels of aspartate transaminase (AST) were evaluated every 3-4 days during the acute infection period, through day 10-14 (FIG. 2D), and then on the last day of the 28-day follow up period (not shown). Plasma AST remained at baseline levels through day 3 after infection in all subjects, indicating normal liver function immediately following infectious EBOV challenge. By day 6 after EBOV exposure, the unvaccinated control subject displayed a 10-fold increase in enzyme levels indicating active infection in this subject. Blood samples from two subjects in the Ad5-nave/rAd35-vaccinated group (V1, V3) also exhibited dramatic increases in AST, while the third subject in this group V2 showed only a marginal increase at a single time point prior to resolution back to baseline levels. Similarly, two of three subjects in the Ad5-immune/rAd35-vaccinated group (V4, V5) displayed elevations in AST, though much lower than the unvaccinated control, while one subject V6 remained normal for this parameter of infection. Overall, AST levels were higher in Ad5-naive than in the Ad5-immune vaccinated subjects. It is noteworthy mentioning that each subject who remained normal for this clinical observation displayed the highest prechallenge, antigen-specific CD8.sup.+ and antibody responses within its respective vaccine group. Plasma viremia levels (FIG. 2E) confirmed EBOV infection in all animals who displayed elevated AST.

(62) The results of this experiment show that rAd35 is immunogenic when administered at a dose of 10.sup.10 particles per subject. The vaccine generated protective immune responses but this dose and regimen was suboptimal for uniform protection of all subjects. Within vaccine groups, protective immunity was associated with the highest magnitude antigen-specific antibody and CD8.sup.+ T-cell responses.

(63) rAd35-GP dose response effects on induction of protective immunity. rAd-based vectors are commonly administered to macaques in doses ranging from 10.sup.10 to 10.sup.12 particles. Previous results with rAd5-GP have demonstrated 10.sup.10 virus particles as the minimal dose to achieve 100% protection of cynomolgus macaques against EBOV infection (Sullivan, 2006). Since the studies described above were performed at the lower end of this dose range and did not result in uniform protection, it is possible that even marginally lower in vivo antigen expression achieved with the rAd35 vector when compared to that of rAd5 vectors could result in suboptimal immune responses. Therefore, we asked whether administration of a higher vaccine dose could elicit a greater degree of immune protection. The vaccine in this experiment also included rAd35 expressing GP from the Sudan EBOV species (S/G) in order to compare efficacy to historical data with rAd5 vaccines that comprised GP from both Sudan and Zaire species. In the present study, cynomolgus macaques (n=3 per group) were vaccinated with 10.sup.10 or 10.sup.11 virus particles each of Ad35BSU.Ebo.GP(Z)FL.wt and Ad35BSU.Ebo.GP(S/G)FL and immune responses were measured three weeks after vaccination in the previous experiment.

(64) GP-specific antibodies were generated in all subjects (FIG. 3A), an expected result since the vaccine dose was equal to or higher than that in the previous experiment. However, the titers in two subjects vaccinated with 10.sup.10 particles in this experiment (V8, V9) were 1:340 and 1:500, respectively, levels near or below the minimum cutoff previously observed to predict protection in Ad5-GP vaccinated subjects (Sullivan, et al., 2009). The maximum antibody titer observed was 1:2,900 (subject V10) which is the same as the maximum titers observed in the rAd35 subjects shown in FIG. 2. Average antibody titers were higher in the 10.sup.11 dose group (1:1500 vs 1:700) but the difference did not reach statistical significance (p=0.02). As observed in the lower dose group, there was one subject whose titer was near the rAd5-GP vaccine cutoff for immune protection (subject V11, 1:540).

(65) CD4.sup.+ and CD8.sup.+ T-cell responses were present in both dose groups at three weeks post vaccination. There was no clear dose response in either CD4.sup.+ or CD8.sup.+ T cell responses. Since the kinetics of cellular immune responses varies between subjects, especially in outbred animals, and the response measurement is not cumulative over time as it is with antibody levels, group trends are sometimes difficult to capture at a single time point. Within each individual, antigen-specific T-cell frequencies were higher for CD4.sup.+ than for CD8.sup.+ cells, but when combined with the results from the first experiment, there was no trend toward either CD4.sup.+ or CD8.sup.+ cell dominance induced by rAd35-GP vectors in these experiments.

(66) One week following the assessment of immune responses, all six vaccinated macaques and one unvaccinated subject were exposed to 1000 PFU ZEBOV by intramuscular injection and observed for signs of productive infection. Hemorrhagic manifestations of EBOV infection routinely result in the appearance of a maculopapular rash on the face and extremities of infected macaques; subjects also typically reduce food intake and become dehydrated. The earliest appearance of symptoms for the two unvaccinated subjects occurred on day 6 after EBOV exposure; each displayed a full constellation of symptoms by day 7 (data not shown). Table 2 shows the infectious challenge outcomes and the day of death in nonsurvivors for both rAd35 studies. The unvaccinated subjects succumbed to the lethal effects of infection on days 9 and 8 (Experiment 1 and 2, respectively). Vaccinated subjects who died were similar to control, unvaccinated subjects, except that they survived on average two days longer than controls, suggesting a potential partial immune benefit of vaccination even though mortality was ultimately observed. The number of survivors was greater in the subjects who received rAd35-GP(Z) only, compared to those receiving GP(Z) plus GP(S/G) irrespective of the vaccine dose, but differences in survival rates were not significant across any vaccine groups in the two challenge experiments.

(67) TABLE-US-00002 TABLE 2 Subject Experiment ID Vaccine Group Symptoms Outcome 1 V1 Naive/ Rash d6, anorexia d6, Died day 7 Ad35BSU.Ebo.GP(Z)FL.wt dehydration d6 at 10.sup.10 V2 Naive/ Anorexia d6 Survived Ad35BSU.Ebo.GP(Z)FL.wt at 10.sup.10 V3 Naive/ Rash d6, anorexia d6, Died day 8 Ad35BSU.Ebo.GP(Z)FL.wt dehydration d6 at 10.sup.10 V4 Immune/ Rash d7, anorexia d6, Died day 8 Ad35BSU.Ebo.GP(Z)FL.wt dehydration d7 at 10.sup.10 V5 Immune/ Rash d6, anorexia d6, Died day 9 Ad35BSU.Ebo.GP(Z)FL.wt dehydration d7 at 10.sup.10 V6 Immune/ Anorexia d6 Survived Ad35BSU.Ebo.GP(Z)FL.wt at 10.sup.10 2 V7 Ad35BSU.Ebo.GP(Z)FL.wt Rash d6, anorexia d6, Died day 6 and dehydration d6 Ad35BSU.Ebo.GP(S/G)FL, each at 10.sup.10 V8 Ad35BSU.Ebo.GP(Z)FL.wt Rash d6, anorexia d6, Died day 10 and dehydration d9 Ad35BSU.Ebo.GP(S/G)FL, each at 10.sup.10 V9 Ad35BSU.Ebo.GP(Z)FL.wt Rash d6, anorexia d6, Died day 6 and dehydration d6 Ad35BSU.Ebo.GP(S/G)FL, each at 10.sup.10 V10 Ad35BSU.Ebo.GP(Z)FL.wt Rash d6, anorexia d6, Died day 7 and dehydration d7 Ad35BSU.Ebo.GP(S/G)FL, each at 10.sup.11 V11 Ad35BSU.Ebo.GP(Z)FL.wt Rash d6, anorexia d6, Died day 7 and dehydration d7 Ad35BSU.Ebo.GP(S/G)FL, each at 10.sup.11 V12 Ad35BSU.Ebo.GP(Z)FL.wt Rash d6, anorexia d6, Died day 8 and dehydration d6 Ad35BSU.Ebo.GP(S/G)FL, each at 10.sup.11 1 C1 None Rash d6, anorexia d6, Died day 9 dehydration d6 2 C2 None Rash d7, anorexia d6, Died day 8 dehydration d6

(68) Altogether, the studies using rAd35 as a vaccine vector with GP(Z) alone or in combination with GP(S/G) showed that antigen delivery and presentation was sufficient to generate antigen-specific immune responses, but at levels below what is required for absolute immune protection. Lower protective immunity was associated with the antibody levels detected in some animals consistent with what has been shown using rAd5 vectors to be marginal for protection.

(69) rAd26-GP vaccine immunogenicity and potency for protection against EBOV infection. We next evaluated a recombinant Ad26-based vaccine, a group D adenovirus, for its ability to generate protective immunity against EBOV infection. This serotype uses the same cellular receptor (CD46) as Ad35 but has been shown to generate slightly higher immune responses when used as a priming vaccine vector (Liu, et al., 2009). For these studies, dose escalation was conducted over a range of three orders of magnitude in two separate infectious challenge experiments. In the first study we tested the vaccine at doses of 10.sup.10 or 10.sup.11 particles for each vector, Ad26.Ebo.GP(Z)FL.wt and Ad26.Ebo.GP(S/G)FL.wt, and in the second study we used a dose of 10.sup.12 particles each. The first study tested the vaccine in Ad5-immune cynomolgus macaques in order to evaluate whether rAd26, like rAd35, could elicit antigen-specific immune response in the presence of pre-existing immunity to Ad5. Four Ad5-immune cynomolgus macaques per group were vaccinated by intramuscular injection, and blood samples were obtained three weeks later to assess circulating humoral and cellular immune responses against EBOV GP (FIG. 4A). The average circulating anti-GP antibody titers showed a dose response across dose groups; 1:700 for 10.sup.10 vaccinees and 1:4500 for subjects receiving 10.sup.11 particles (p=0.06). The average titer for three of four subjects in the 10.sup.10 dose group was just above the minimum threshold for immune protection in rAd5-vaccinated subjects (1:500), but subject V16 generated only a marginal antibody response, 1:100, which was well below the predicted protection cutoff for an Ad5-GP vaccine. In contrast, subject V19 who was vaccinated with 10.sup.11 particles of the rAd26 vaccine generated a very high antibody titer, 1:10,500, exceeding by nearly three-fold the level that has been associated with complete immune protection (1:3,500), while the others in this vaccine group displayed intermediate titers that do not definitively predict survival outcome. In study two, four subjects received 10.sup.12 particles of each rAd26 vector and generated antibody responses very similar to those in the 10.sup.11 dose group, with the majority of subject's titers between 1:1000-1:4000. The average anti-GP antibody titer for this group was 1:3000.

(70) T-cell immune responses (FIGS. 4B and 4C) were measured by ICS as in the rAd35 studies and also trended toward a dose response in study one, but the difference between 10.sup.10 and 10.sup.11 dose groups was not significant (p=0.12 and 0.26 for CD4.sup.+ and CD8.sup.+, respectively). Average antigen-specific CD4.sup.+ T-cell frequencies were 0.14% for vaccinees receiving 10.sup.10 particles rAd26-GP versus 0.24% at the higher vaccine dose, and one vaccinee in the lower dose group, subject V14, had an undetectable CD4.sup.+ response (FIG. 4B). The rAd26 vaccine did not skew cellular immune responses toward either CD4.sup.+ or CD8.sup.+ dominance; the CD8.sup.+ frequencies, 0.13% and 0.25% (10.sup.10 and 10.sup.11 vaccine doses, respectively) essentially mirrored the magnitude of CD4.sup.+ responses. In the case of CD8.sup.+ T cells, there were two subjects in the low dose group, V13 and V14, with undetectable antigen-specific responses (FIGS. 4B and 4C). In rAd26 study two, average antigen-specific CD8.sup.+ frequencies (0.34%) were higher than CD4.sup.+ responses (0.08%) but this apparent skewing toward CD8.sup.+ responses was driven primarily by a single subject, V24, who had very high CD8.sup.+ frequencies and low CD4.sup.+ responses. Otherwise, overall cellular immune responses were similar to those observed in rAd26 study one.

(71) Infectious EBOV challenges were performed by IM injection of 1000 PFU ZEBOV at 4 weeks after vaccination for each of the rAd26 vaccine studies, and liver enzyme levels were measured to monitor disease (FIG. 4D). Unvaccinated subjects exhibited manifestations of hepatic injury between days 3 and 6 of infection. All subjects receiving the lowest dose rAd26 vaccine, 10.sup.10 particles, showed similar signs disease, though AST levels increased at a slower rate. As predicted from this clinical indicator, all subjects in this group succumbed to the lethal effects of infection by day 8 post ZEBOV challenge (FIG. 5A). The antibody and T-cell responses were low or undetectable in some subjects in this group. Differences in the magnitude of immune responses between the dose groups in Ad26 study one (10.sup.10 and 10.sup.11) were generally reflected in the survival rates, with a higher survival outcome, 2 out of 4 protected, in subjects vaccinated with 10.sup.11 particles of rAd26-GP (p=0.01). Ad26 at 10.sup.11 particles was superior not only to the lower dose, but also provided greater protection than rAd35-GP when matched for dosage (FIG. 5B). Finally, rAd26 given at a dose of 10.sup.12 particles yielded the highest number of survivors (3 out of 4) for any vaccine regimen tested in these studies, and the level of immune protection did not differ significantly from what has been observed previously with rAd5 vectors (p=0.32, FIG. 5C); however, this survival rate was obtained using a higher dose for rAd26 than for rAd5, 10.sup.12 vs. 10.sup.10 particles, respectively, suggesting a potential potency difference between these vectors in this animal model.

(72) Heterologous Prime-Boost with rAd26 and rAd35 Vectors. The dose-response characteristics for rAd26-GP-mediated immune protection and the high survival outcome using 10.sup.12 vector particles suggested that this vector efficiently induces GP-antigen expression. Since it has been shown for EBOV and other pathogens, in both nonhuman and human subjects, that heterologous prime-boost vaccination can elicit more potent immunity than single shot immunization (Sullivan Nature 2000; Sampra et al., Vaccine 27 (2009) 5837-5845; Koup, et al, PLoS One 2010; Geisbert et al., (2010) Virol 84(19): 10386-94), we asked whether rAd26-GP immune responses could be boosted with a heterologous vector to improve protection against EBOV infection. Four cynomolgus macaques were inoculated with 10.sup.11 particles each of Ad26.Ebo.GP(Z)FL.wt and Ad26.Ebo.GP(S/G)FL.wt. One month later, all subjects received a boost vaccination with the same dose of Ad35BSU.Ebo.GP(Z)FL.wt and Ad35BSU.Ebo.GP(S/G)FL. Immune responses were assessed immediately prior to, and three weeks following the boost. FIG. 6A shows that antibody responses against EBOV-GP(Z) were efficiently induced by the priming vaccination. Individual subjects generated EC90 antibody titers against GP from 1:2700 to 1:7100, and the average titer for the group was 1:4000, consistent with the responses observed in the previous study testing 10.sup.11 rAd26 as a single inoculation vaccine (1:4500). This study included for comparison a single subject inoculated with 10.sup.10 particles each of rAd5-GP(Z) and rAd5-GP(S/G), whose post vaccination antibody titer was 1:6800. Subsequent inoculation of the rAd26-GP-primed subjects with 10.sup.11 particles of rAd35-GP vectors boosted antigen-specific antibody levels approximately one order of magnitude for most vaccinees to an average titer of 1:32,000, except subject V27 whose post-prime antibody titers were exceptionally high. Interestingly, the boost vaccination generated more uniform titers across subjects, with a standard deviation across subjects of just under 10%, compared to the post prime titers that exhibited a standard deviation of 54%.

(73) Cellular immune responses were also boosted markedly by rAd35-GP administration to rAd26-vaccinated macaques (FIGS. 6B and 6C). CD4.sup.+ T cells were boosted in all except in one subject, V25; the average increase after rAd35-GP administration was 2-fold across all subjects and boosting revealed a measurable response in subject V27 whose response was undetectable prior to boosting. Final, post-boost CD4.sup.+ T-cell frequencies were comparable to those generated by rAd5-GP vaccination. The boost effect was greatest for CD8.sup.+ T cells and all subjects exhibited the boost effect in this cellular compartment yielding, in two subjects (V27 and V28), responses exceeding those generated by rAd5-GP vaccination. Average GP-specific CD8+ T-cell frequencies measured by ICS were 0.09% after primary immunization, and increased 4.7-fold to 0.41%, 3 weeks after secondary vaccination with rAd35-GP.

(74) Altogether, the immunogenicity results above showed that rAd35-GP vectors are potent for boosting rAd26-GP primed macaques. Post-boost GP-directed antibodies were induced to an average level that is nearly a log higher than the level predictive for 100% immune protection in rAd5-GP vaccinated primates (Sullivan, et al., 2009). Importantly, rAd35-GP boost provided a substantial enhancement of CD8.sup.+ T-cell frequencies, also shown to associate with immune protection against EBOV infection. Therefore, one week after assessment of immune responses (4-weeks post boost) all vaccinated subjects and one unvaccinated control macaque were exposed to 1000 PFU of ZEBOV by intramuscular injection. The control subject exhibited clinical symptoms characteristic of EBOV infection and succumbed to lethal effects at day 6 after challenge (FIGS. 6C and 6D). In contrast, all vaccinated subjects remained normal for circulating AST levels (FIG. 6C), and exhibited no evidence of hemorrhagic disease in gross pathology evaluation at study termination (not shown). All four vaccinated subjects survived infectious challenge and remained symptom-free throughout the 28-day follow up period until study termination. These results showed that rAd26/rAd35 vectors administered as a heterologous prime boost vaccine regimen provides uniform immune protection against ZEBOV infection, and demonstrate the potential utility of this approach for achieving additive or synergistic results with combination vaccines.

(75) Discussion

(76) Adenoviruses perform well as vaccine vectors for the delivery of a variety of viral bacterial and parasitic antigens (Lasaro et al., (2009) Mol Ther 17(8): 1333-9). rAd5 vectors in particular generate potent antigen-specific immune responses in mice, nonhuman primates, and humans, as we have observed when EBOV-GP is the target antigen. However, preclinical and human clinical studies have suggested that the potency of rAd5-based vectors may be compromised in individuals who have been exposed previously to Ad5 if they have high level of immunity against the vector. The aim of the studies herein was to identify rAd vectors that can deliver the EBOV GP antigen in both nave and Ad5-immune subjects. Since pre-existing immunity against any viral vector has the potential to limit its effectiveness, we focused our attention on viruses that infect humans relatively rarely, as indicated by the prevalence of seropositive subjects and/or the low levels of neutralizing antibodies. The rare human adenovirus serotypes, Ad35 and Ad26 were selected for vaccine development in the current work.

(77) rAd35-GP vaccination of macaques generated antigen-specific antibody and T-cell responses in individual subjects within the range observed previously when rAd5 was used as the delivery vector. The average anti-GP antibody titer for all rAd35 vaccinees (irrespective of dose), 1:1400 was lower than the average for all historical subjects vaccinated with 10.sup.10 rAd5-GP (1:11,000, n=17), providing an initial indication that vector potency might differ between the two serotypes if antibody titer is the same correlate for rAd35 as it is for rAd5 EBOV vaccines. CD4.sup.+ and CD8.sup.+ T-cell responses were detectable in most subjects prior to infectious challenge, though the absolute magnitude cannot be compared to rAd5 vaccinees not included in these studies in the absence of PBMC samples for assay bridging controls.

(78) Vaccination with rAd35 vectors effectively induced antigen-specific antibody and T-lymphocyte immune responses in either rAd5-nave or rAd5-immune subjects, suggesting that rare serotype vector genomes are sufficiently distant from common serotypes to resist heterologous vector-directed immunity. This feature of vector performance will be important to circumvent pre-existing immunity stemming not only from natural viral infection, but also from the use of heterologous vectors in priming immunizations or vaccination against other pathogens. Indeed, rAd35-GP inoculation provided a potent boost of both cell-mediated and antibody responses in macaques primed with rAd26-GP. This result was intriguing since it demonstrates a clear difference in vector potency for the induction of secondary versus primary immune responses; the ability of rAd35-GP to boost the immune response was not predicted by the magnitude of responses observed after the priming immunization. These data may indicate that rAd35 and other rAd vectors have a higher transduction efficiency in certain populations or activation states of target dendritic cells, as suggested recently by Lindsay et al., J Immunol 185 (3): 1513-21, that may, in this case, be more abundant or accessible during secondary immune responses.

(79) rAd26 proved to be more potent than rAd35 as a single shot vaccine against EBOV infection, mediating survival in up to 75% of vaccinated macaques at the highest dose tested. rAd26-GP vaccines demonstrated a clear dose-response for the induction of protective immunity, suggesting that marginal improvements in antigen expression could increase the potency of rAd26-based vaccines to generated uniform protection against high doses of EBOV challenge, such as those used herein. Interestingly, the higher degree of protection offered by rAd26-GP vectors compared to rAd35-GP at a matched dose (10.sup.11 particles) associated with higher ELISA anti-GP titers, 1:4500 versus 1:1400, respectively. These data highlight the possibility that prechallenge antibody titers may serve as an immune correlate of protection against ZEBOV infection across rAd serotypes in addition to within vector groups as has been observed for rAd5-GP vaccines. The order of potency for induction of antibody responses predicted the rank order for protection across vector groups.

(80) The studies herein tested vaccine vectors that were compared singly and in combination and demonstrate the utility of alternative serotype rAds for use as vaccine vectors in primates. The results suggest that these vaccines may be most useful in a prime-boost combination.

(81) Because of the high magnitude of antigen-specific responses achieved by heterologous prime-boost, it has been proposed that long term-immunity may be optimally achieved by priming rAd with DNA (Santra, et al., (2005). J Virol 79(10): 6516-22). Since DNA requires multiple primes and does not induce rapid protection like rAd vectors do, heterologous rAd prime-boost may provide an optimal opportunity to generate a balance between the induction of rapid, and long lasting protective immunity.

(82) It is understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and scope of the appended claims. All publications, patents, and patent applications cited herein are hereby incorporated by reference in their entirety for all purposes.