T-Cell Correlates of Vaccine Efficacy after a Heterologous Simian Immunodeficiency Virus Challenge
Year: 2010
Type: article
Abstract: Determining the "correlates of protection" is one of the challenges in human immunodeficiency virus vaccine design. To date, T-cell-based AIDS vaccines have been evaluated with validated techniques that measure the number of CD8(+) T cells in the blood that secrete cytokines, mainly gamma interferon (IFN-gamma), in response to synthetic peptides. Despite providing accurate and reproducible measurements of immunogenicity, these methods do not directly assess antiviral function and thus may not identify protective CD8(+) T-cell responses. To better understand the correlates of vaccine efficacy, we analyzed the immune responses elicited by a successful T-cell-based vaccine against a heterologous simian immunodeficiency virus challenge. We searched for correlates of protection using a viral suppression assay (VSA) and an IFN-gamma enzyme-linked immunospot assay. While the VSA measured in vitro suppression, it did not predict the outcome of the vaccine trial. However, we found several aspects of the vaccine-induced T-cell response that were associated with improved outcome after challenge. Of note, broad vaccine-induced prechallenge T-cell responses directed against Gag and Vif correlated with lower viral loads and higher CD4(+) lymphocyte counts. These results may be relevant for the development of T-cell-based AIDS vaccines since they indicate that broad epitope-specific repertoires elicited by vaccination might serve as a correlate of vaccine efficacy. Furthermore, the present study demonstrates that certain viral proteins may be more effective than others as vaccine immunogens.
Source: Journal of Virology
DOI: 10.1128/jvi.02365-09
Language: English
Topic: HIV Research and Treatment
Subfield: Virology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: green
Awards: G1344557351, EXTRAMURAL RESEARCH FACILITIES CONSTRUCTION, A Novel, Logical Approach to HIV Vaccine Development, G286789154, MHC Typing of Macaques Used in AIDS Research, The Functional Significance of CTL Escape, Vaccine Regimens to Induce CD4+ and CD8+ T cells against SIV Epitopes, EXTRAMURAL REGIONAL FACILITIES CONSTRUCTION, Minigene Vaccination with Early Presented Viral Proteins, MHC-bound, SIV-derived, CTL and HTL Epitopes, G832415928, G9000017745, Wisconsin National Primate Research Center Support
OpenAlex ID: W2144739516
