Longitudinal Analysis of Human Immunodeficiency Virus Type 1‐Specific Cytotoxic T Lymphocyte Responses: A Predominant Gag‐Specific Response Is Associated with Nonprogressive Infection
Author(s) -
Oscar Pontesilli,
Michèl R. Klein,
Susana R. KerkhofGarde,
Nadine G. Pakker,
Frank de Wolf,
Hanneke Schuitemaker,
Frank Miedema
Publication year - 1998
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/515659
Subject(s) - ctl* , cytotoxic t cell , immunology , virology , cellular immunity , virus , biology , group specific antigen , t lymphocyte , immune system , immunity , peripheral blood mononuclear cell , hiv antigens , lymphocyte , lentivirus , cd8 , viral disease , in vitro , biochemistry
To establish correlates of protective immunity during human immunodeficiency virus type 1 (HIV-1) infection, the frequencies of circulating cytotoxic T lymphocyte (CTL) precursors (p) directed against 4 HIV-1 gene products (reverse transcriptase, gag, nef, and env) were evaluated in HIV-1-infected homosexual men who progressed to AIDS and in long-term survivors over time. For both groups, HIV-1-specific CTL responses had similar kinetics and magnitude. At maximum expansion, HIV-1-specific CTLp had a median frequency of 0.2% mononuclear cells in both progressors and long-term survivors, with peaks of 0.5% and 2%, respectively. Long-term survivors maintained the established CTLp pool and presented a persistently predominant gag-specific response. The fraction and, to a lesser extent, the frequency of gag-specific CTLp were inversely correlated with virus load. In progressors, general T cell function and measurable HIV-1-specific CTLp frequencies dropped simultaneously, suggesting a further loss of virus control due to the ensuing immunodeficiency.
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