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PMID: 10878387 Published · ppublish English Journal Article

Maintenance of large numbers of virus-specific CD8+ T cells in HIV-infected progressors and long-term nonprogressors.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 165 ·No. 2 ·2000-07-15 ·Pages 1082-92

Gea-Banacloche JC, Migueles SA, Martino L, Shupert WL, McNeil AC, Sabbaghian MS, Ehler L, Prussin C, Stevens R, Lambert L, Altman J, Hallahan CW, de Quiros JC, Connors M

Abstract

The virus-specific CD8+ T cell responses of 21 HIV-infected patients were studied including a unique cohort of long-term nonprogressors with low levels of plasma viral RNA and strong proliferative responses to HIV Ags. HIV-specific CD8+ T cell responses were studied by a combination of standard cytotoxic T cell (CTL) assays, MHC tetramers, and TCR repertoire analysis. The frequencies of CD8+ T cells specific to the majority of HIV gene products were measured by flow cytometric detection of intracellular IFN-gamma in response to HIV-vaccinia recombinant-infected autologous B cells. Very high frequencies (0.8-18.0%) of circulating CD8+ T cells were found to be HIV specific. High frequencies of HIV-specific CD8+ T cells were not limited to long-term nonprogressors with restriction of plasma virus. No correlation was found between the frequency of HIV-specific CD8+ T cells and levels of plasma viremia. In each case, the vast majority of cells (up to 17.2%) responded to gag-pol. Repertoire analysis showed these large numbers of Ag-specific cells were scattered throughout the repertoire and in the majority of cases not contained within large monoclonal expansions. These data demonstrate that high numbers of HIV-specific CD8+ T cells exist even in patients with high-level viremia and progressive disease. Further, they suggest that other qualitative parameters of the CD8+ T cell response may differentiate some patients with very low levels of plasma virus and nonprogressive disease.

MeSH Terms
Adult Amino Acid Sequence Cytotoxicity Tests, Immunologic Cytotoxicity, Immunologic Disease Progression Epitopes, T-Lymphocyte/analysis,genetics,immunology Female HIV Antigens/immunology HIV Infections/immunology,metabolism,pathology,virology Humans Interferon-gamma/metabolism Lymphocyte Count Male Middle Aged Molecular Sequence Data Receptors, Antigen, T-Cell, alpha-beta/analysis,genetics T-Lymphocytes, Cytotoxic/immunology,metabolism,virology
Chemicals
Epitopes, T-Lymphocyte HIV Antigens Receptors, Antigen, T-Cell, alpha-beta Interferon-gamma
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Gea-Banacloche J C
Laboratories ofImmunoregulation and Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Migueles S A
Martino L
Shupert W L
McNeil A C
Sabbaghian M S
Ehler L
Prussin C
Stevens R
Lambert L
Altman J
Hallahan C W
de Quiros J C
Connors M
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
2000-07-15
Pages
1082-92
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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