Protection Afforded by an HIV Vaccine Candidate in Macaques Depends on the Dose of SIV mac251 at Challenge Exposure

Author:

Vaccari Monica1,Keele Brandon F.2,Bosinger Steven E.3,Doster Melvin N.1,Ma Zhong-Min4,Pollara Justin5,Hryniewicz Anna1,Ferrari Guido5,Guan Yongjun6,Forthal Donald N.7,Venzon David8,Fenizia Claudio1,Morgan Tia1,Montefiori David5,Lifson Jeffrey D.2,Miller Chris J.4,Silvestri Guido3,Rosati Margherita9,Felber Barbara K.10,Pavlakis George N.9,Tartaglia James11,Franchini Genoveffa1

Affiliation:

1. Animal Models and Retroviral Vaccine Section, National Cancer Institute, Bethesda, Maryland, USA

2. AIDS and Cancer Virus Program, SAIC Frederick, Inc., Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA

3. Yerkes National Primate Research Center, Emory Vaccine Center, Emory University, Atlanta, Georgia, USA

4. California National Primate Research Center, University of California Davis, Davis, California, USA

5. Department of Surgery, Duke University, Durham, North Carolina, USA

6. Institute of Human Virology and Department of Microbiology & Immunology, University of Maryland School of Medicine, Baltimore, Maryland, USA

7. University of California, Irvine, Irvine, California, USA

8. Biostatistics and Data Management Section, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA

9. Human Retrovirus Section, Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA

10. Human Retrovirus Pathogenesis Section, Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA

11. Sanofi Pasteur, Inc., Swiftwater, Pennsylvania, USA

Abstract

ABSTRACT We used the simian immunodeficiency virus mac251 (SIV mac251 ) macaque model to study the effect of the dose of mucosal exposure on vaccine efficacy. We immunized macaques with a DNA prime followed by SIV gp120 protein immunization with ALVAC-SIV and gp120 in alum, and we challenged them with SIV mac251 at either a single high dose or at two repeated low-dose exposures to a 10-fold-lower dose. Infection was neither prevented nor modified following a single high-dose challenge of the immunized macaques. However, two exposures to a 10-fold-lower dose resulted in protection from SIV mac251 acquisition in 3 out of 12 macaques. The remaining animals that were infected had a modulated pathogenesis, significant downregulation of interferon responsive genes, and upregulation of genes involved in B- and T-cell responses. Thus, the choice of the experimental model greatly influences the vaccine efficacy of vaccines for human immunodeficiency virus (HIV).

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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