Literature DB >> 21490096

Vesicular stomatitis virus-simian retrovirus type 2 vaccine protects macaques from detectable infection and B-cell destruction.

Rajeev Gautam1, Arun Iyer, Meredith Hunter, Arpita Das, Tessa Williams, Jason Dufour, Cristian Apetrei, K Gus Kousoulas, Preston A Marx.   

Abstract

Natural infection with simian retrovirus (SRV) has long been recognized in rhesus macaques (RMs) and may result in an AIDS-like disease. Importantly, SRV infections persist as a problem in recently imported macaques. Therefore, there is a clear need to control SRV spread in macaque colonies. We developed a recombinant vesicular stomatitis virus (VSV)-SRV vaccine consisting of replication-competent hybrid VSVs that express SRV gag and env in separate vectors. The goal of this study was to assess the immunogenicity and protective efficacy of the VSV-SRV serotype 2 vaccine prime-boost approach in RMs. The VSV-SRV vector (expressing either SRV gag or env) vaccines were intranasally administered in 4 RMs, followed by a boost 1 month after the first vaccination. Four RMs served as controls and received the VSV vector alone. Two months after the boost, all animals were intravenously challenged with SRV-2 and monitored for 90 days. After the SRV-2 challenge, all four controls became infected, and viral loads (VLs) ranged from 10(6) to 10(8) SRV RNA copies/ml of plasma. Two animals in the control group developed simian AIDS within 7 to 8 weeks postinfection and were euthanized. Anemia and weight loss were observed in the remaining controls. During acute infection, severe B-cell depletion and no significant changes in T-cell population were observed in the control group. Control RMs with greater preservation of B cells and lower VLs survived longer. SRV-2 was undetectable in vaccinated animals, which remained healthy, with no clinical or biological signs of infection and preservation of B cells. Our study showed that the VSV-SRV vaccine is a strong approach for preventing clinically relevant type D retrovirus infection and disease in RMs, with protection of 4/4 RMs from SRV infection and prevention of B-cell destruction. B-cell protection was the strongest correlate of the long-term survival of all vaccinated and control RMs.

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Year:  2011        PMID: 21490096      PMCID: PMC3126322          DOI: 10.1128/JVI.02523-10

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  41 in total

1.  Protection of macaques against infection with simian type D retrovirus (SRV-1) by immunization with recombinant vaccinia virus expressing the envelope glycoproteins of either SRV-1 or Mason-Pfizer monkey virus (SRV-3).

Authors:  B A Brody; E Hunter; J D Kluge; R Lasarow; M Gardner; P A Marx
Journal:  J Virol       Date:  1992-06       Impact factor: 5.103

2.  Isolation and characterization of the neutralizable epitope of simian retrovirus-1 (SRV-1) and of the cell receptor for the virus.

Authors:  E Benjamini; J V Torres; L L Werner; A Malley
Journal:  Adv Exp Med Biol       Date:  1991       Impact factor: 2.622

Review 3.  Nonhuman primate retrovirus isolates and AIDS.

Authors:  M B Gardner; P Luciw; N Lerche; P Marx
Journal:  Adv Vet Sci Comp Med       Date:  1988

4.  Long-term protection of macaques against high-dose type D retrovirus challenge after immunization with recombinant vaccinia virus expressing envelope glycoproteins.

Authors:  R E Benveniste; L Kuller; S T Roodman; S L Hu; W R Morton
Journal:  J Med Primatol       Date:  1993 Feb-May       Impact factor: 0.667

5.  Neutralization epitope in the envelope glycoprotein of simian retrovirus-1 (SRV-1) and identification of the virus receptor.

Authors:  J V Torres; L L Werner; A Malley; E Benjamin
Journal:  J Med Primatol       Date:  1991-06       Impact factor: 0.667

6.  Protection of macaques against simian AIDS by immunization with a recombinant vaccinia virus expressing the envelope glycoproteins of simian type D retrovirus.

Authors:  S L Hu; J M Zarling; J Chinn; B M Travis; P A Moran; J Sias; L Kuller; W R Morton; G Heidecker; R E Benveniste
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

7.  Viremia, antigenemia, and serum antibodies in rhesus macaques infected with simian retrovirus type 1 and their relationship to disease course.

Authors:  H S Kwang; N C Pedersen; N W Lerche; K G Osborn; P A Marx; M B Gardner
Journal:  Lab Invest       Date:  1987-06       Impact factor: 5.662

8.  Cytoplasmic domain requirement for incorporation of a foreign envelope protein into vesicular stomatitis virus.

Authors:  R J Owens; J K Rose
Journal:  J Virol       Date:  1993-01       Impact factor: 5.103

9.  A plasma membrane localization signal in the HIV-1 envelope cytoplasmic domain prevents localization at sites of vesicular stomatitis virus budding and incorporation into VSV virions.

Authors:  J E Johnson; W Rodgers; J K Rose
Journal:  Virology       Date:  1998-11-25       Impact factor: 3.616

10.  Simian retrovirus-D serotype 1 (SRV-1) envelope glycoproteins gp70 and gp20: expression in yeast cells and identification of specific antibodies in sera from monkeys that recovered from SRV-1 infection.

Authors:  H S Kwang; P J Barr; E A Sabin; S Sujipto; P A Marx; M D Power; I C Bathurst; N C Pedersen
Journal:  J Virol       Date:  1988-05       Impact factor: 5.103

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  3 in total

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Authors:  Gabrielle Scher; Matthias J Schnell
Journal:  Curr Opin Virol       Date:  2020-10-29       Impact factor: 7.090

2.  Simian retrovirus 4 induces lethal acute thrombocytopenia in Japanese macaques.

Authors:  Rokusuke Yoshikawa; Munehiro Okamoto; Shoichi Sakaguchi; So Nakagawa; Tomoyuki Miura; Hirohisa Hirai; Takayuki Miyazawa
Journal:  J Virol       Date:  2015-01-21       Impact factor: 5.103

Review 3.  Specific pathogen free macaque colonies: a review of principles and recent advances for viral testing and colony management.

Authors:  JoAnn L Yee; Thomas H Vanderford; Elizabeth S Didier; Stanton Gray; Anne Lewis; Jeffrey Roberts; Kerry Taylor; Rudolf P Bohm
Journal:  J Med Primatol       Date:  2016-03-01       Impact factor: 0.667

  3 in total

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