Human immunodeficiency virus type 1 (HIV-1) antigen secretion by latently infected resting CD4+ T lymphocytes from HIV-1-infected individuals

被引:16
作者
Fondere, JM
Petitjean, G
Huguet, MF
Salhi, SL
Baillat, V
Macura-Biegum, A
Becquart, P
Reynes, J
Vendrell, JP
机构
[1] Hop Lapeyronie, Virol Lab, F-34295 Montpellier, France
[2] CNRS, UMR 5160, Ctr Pharmacol & Biotechnol Sante, Fac Pharm, Montpellier, France
[3] Hop Gui De Chauliac, Dept Maladies Infect & Trop, Montpellier, France
[4] Inst Rech Dev, UR 36, Montpellier, France
[5] INSERM, U475, Montpellier, France
[6] Jagiellonian Univ, Dept Clin Immunol, Polish Amer Inst Pediat, Coll Med, Krakow, Poland
关键词
D O I
10.1128/JVI.78.19.10536-10542.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In resting CD4(+) T lymphocytes harboring human immunodeficiency virus type 1 (HIV-1), replication-competent virus persists in patients responding to highly active antiretroviral therapy (HAART). This small latent reservoir represents between 10(3) and 10(7) cells per patient. However, the efficiency of HIV-1 DNA-positive resting CD4(+) T cells in converting to HIV-1-antigen-secreting cells (HIV-1-Ag-SCs) after in vitro CD4(+)-T-cell polyclonal stimulation has not been satisfactorily evaluated. By using an HIV-1-antigen enzyme-linked immunospot assay, 8 HIV-1-Ag-SCs per 10(6) CD4(+) resting T cells were quantified in 25 patients with a plasma viral load of <20 copies/ml, whereas 379 were enumerated in 10 viremic patients. In parallel, 369 and 1,238 copies of HIV-1 DNA per 10(6) CD4(+) T cells were enumerated in the two groups of patients, respectively. Only a minority of latently HIV-1 DNA-infected CD4(+) T cells could be stimulated in vitro to become HIV-1-Ag-SCs, particularly in aviremic patients. The difference between the number of HIV-1 immunospots in viremic versus aviremic patients could be explained by HIV-1 unintegrated viral DNA that gave additional HIV-1-Ag-SCs after in vitro CD4(+)-T-cell polyclonal stimulation. The ELISPOT approach to targeting the HIV-1-Ag-SCs could be a useful method for identifying latently RIV-1-infected CD4(+) T cells carrying replication-competent HIV-1 in patients responding to HAART.
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页码:10536 / 10542
页数:7
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