Analysis of HIV-1- and CMV-specific memory CD4 T-cell responses during primary and chronic infection

被引:81
|
作者
Harari, A
Rizzardi, GP
Ellefsen, K
Ciuffreda, D
Champagne, P
Bart, PA
Kaufmann, D
Telenti, A
Sahli, R
Tambussi, G
Kaiser, L
Lazzarin, A
Perrin, L
Pantaleo, G [1 ]
机构
[1] Univ Lausanne, CHU Vaudois, Dept Med, Lab AIDS Immunopathogenesis,Div Immunol, CH-1011 Lausanne, Switzerland
[2] Univ Lausanne, CHU Vaudois, Dept Med, Lab AIDS Immunopathogenesis,Div Allergy & Infect, CH-1011 Lausanne, Switzerland
[3] Univ Lausanne, CHU Vaudois, Inst Microbiol, CH-1011 Lausanne, Switzerland
[4] San Raffaele Inst, Div Infect Dis, Milan, Italy
[5] Univ Geneva, Virol Lab, CH-1211 Geneva 4, Switzerland
关键词
D O I
10.1182/blood-2001-11-0080
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CD4 T-cell-specific memory antiviral responses to human immunodeficiency virus type 1 (HIV-1) and cytomegalovirus (CMV) were investigated in 16 patients with documented primary HIV-1 infection (4 of the 16 subjects also had primary CMV infection) and compared with those observed in patients with chronic HIV-1 and CMV coinfection. Virus-specific memory CD4 T cells were characterized on the basis of the expression of the chemokine receptor CCR7. HIV-1- and CMV-specific interferon-gamma-secreting CD4 T cells were detected in patients with primary and chronic HIV-1 and CMV coinfection and were mostly contained in the cell population lacking expression of CCR7. The magnitude of the primary CMV-specific CD4 T-cell response was significantiy greater than that of chronic CMV infection, whereas there were no differences between primary and chronic HIV1-specific CD4 T-cell responses. A substantial proportion of CD4(+)CCR7(-) T cells were infected with HIV-1. These results advance the characterization of antiviral memory CD4 T-cell response and the delineation of the potential mechanisms that likely prevent the generation of a robust CD4 T-cell immune response during primary infection. (C) 2002 by The American Society of Hematology.
引用
收藏
页码:1381 / 1387
页数:7
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