Control of Human Immunodeficiency Virus Type 1 Is Associated with HLA-B*13 and Targeting of Multiple Gag-Specific CD8<sup>+</sup>T-Cell Epitopes

Isobella Honeyborne(Harvard University), Andrew J. Prendergast(Harvard University), Florencia Pereyra(Harvard University), Alasdair Leslie(Harvard University), Hayley Crawford(Harvard University), Rebecca Payne(Harvard University), Shabashini Reddy(University of KwaZulu-Natal), Karen Bishop(University of KwaZulu-Natal), Eshia Moodley(University of KwaZulu-Natal), K. Narayanan Nair(University of KwaZulu-Natal), Mary van der Stok(University of KwaZulu-Natal), Noel McCarthy(Medawar Building for Pathogen Research), Christine Rousseau(University of Washington), Marylyn M. Addo(Harvard University), James I. Mullins(University of Washington), Christian Brander(Harvard University), Photini Kiepiela(University of KwaZulu-Natal), Bruce D. Walker(Harvard University), Philip Goulder(Harvard University)
Journal of Virology
January 25, 2007
Cited by 145

Abstract

To better understand relationships between CD8+ T-cell specificity and the immune control of human immunodeficiency virus type 1 (HIV-1), we analyzed the role of HLA-B*13, an allele associated with low viremia, in a cohort of 578 C clade-infected individuals in Durban, South Africa. Six novel B*13-restricted cytotoxic T lymphocyte epitopes were defined from analyses of 37 B*13-positive subjects, including three Gag epitopes. These B*13-restricted epitopes contribute to a broad Gag-specific CD8+ response that is associated with the control of viremia. These data are consistent with data from studies of other HLA-class I alleles associated with HIV control that have shown that the targeting of multiple Gag epitopes is associated with relative suppression of viremia.


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