Correlates of nontransmission in US women at high risk of human immunodeficiency virus type 1 infection through sexual exposure

被引:56
作者
Skurnick, JH
Palumbo, P
DeVico, A
Shacklett, BL
Valentine, FT
Merges, M
Kamin-Lewis, R
Mestecky, J
Denny, T
Lewis, GK
Lloyd, J
Praschunus, R
Baker, A
Nixon, DF
Stranford, S
Gallo, R
Vermund, SH
Louria, DB
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Prevent Med & Community Hlth, Newark, NJ 07103 USA
[2] Univ Maryland, Dept Microbiol & Immunol, Baltimore, MD 21201 USA
[3] Univ Maryland, Inst Human Virol, Baltimore, MD 21201 USA
[4] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10021 USA
[5] NYU, Sch Med, Dept Med, New York, NY USA
[6] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[7] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[8] Univ Alabama Birmingham, Div Geog Med, Birmingham, AL 35294 USA
[9] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
关键词
D O I
10.1086/338830
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Seventeen women who were persistently uninfected by human immunodeficiency virus type 1 (HIV-1), despite repeated sexual exposure, and 12 of their HIV-positive male partners were studied for antiviral correlates of nontransmission. Thirteen women had greater than or equal to 1 immune response in the form of CD8 cell noncytotoxic HIV-1 suppressive activity, proliferative CD4 cell response to HIV antigens, CD8 cell production of macrophage inflammatory protein-1beta, or ELISPOT assay for HIV-1-specific interferon-gamma secretion. The male HIV-positive partners without AIDS had extremely high CD8 cell counts. All 8 male partners evaluated showed CD8 cell-related cytotoxic HIV suppressive activity. Reduced CD4 cell susceptibility to infection, neutralizing antibody, single-cell cytokine production, and local antibody in the women played no apparent protective role. These observations suggest that the primary protective factor is CD8 cell activity in both the HIV-positive donor and the HIV-negative partner. These findings have substantial implications for vaccine development.
引用
收藏
页码:428 / 438
页数:11
相关论文
共 51 条
[1]   Human immunodeficiency virus (HIV)-specific cytotoxic T lymphocyte activity in HIV-exposed seronegative persons [J].
Bernard, NF ;
Yannakis, CM ;
Lee, JS ;
Tsoukas, CM .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (03) :538-547
[2]   Epidemiologic and biologic characterization of a cohort of human immunodeficiency virus type I highly exposed, persistently seronegative female sex workers in northern Thailand [J].
Beyrer, C ;
Artenstein, AW ;
Rugpao, S ;
Stephens, H ;
VanCott, TC ;
Robb, ML ;
Rinkaew, M ;
Birx, DL ;
Khamboonruang, C ;
Zimmerman, PA ;
Nelson, KE ;
Natpratan, C .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (01) :59-67
[3]   Factors contributing to the lack of human immunodeficiency virus type 1 (HIV-1) transmission in HIV-1-discordant partners [J].
Bienzle, D ;
MacDonald, KS ;
Smaill, FM ;
Kovacs, C ;
Baqi, M ;
Courssaris, B ;
Luscher, MA ;
Walmsley, SL ;
Rosenthal, KL .
JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (01) :123-132
[4]   OPTIMAL CONDITIONS FOR RECOVERY OF THE HUMAN IMMUNODEFICIENCY VIRUS FROM PERIPHERAL-BLOOD MONONUCLEAR-CELLS [J].
CASTRO, BA ;
WEISS, CD ;
WIVIOTT, LD ;
LEVY, JA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (11) :2371-2376
[5]   IDENTIFICATION OF RANTES, MIP-1-ALPHA, AND MIP-1-BETA AS THE MAJOR HIV-SUPPRESSIVE FACTORS PRODUCED BY CD8(+) T-CELLS [J].
COCCHI, F ;
DEVICO, AL ;
GARZINODEMO, A ;
ARYA, SK ;
GALLO, RC ;
LUSSO, P .
SCIENCE, 1995, 270 (5243) :1811-1815
[6]  
Denny T N, 1998, Int J Infect Dis, V2, P186, DOI 10.1016/S1201-9712(98)90050-9
[8]  
DEVITO C, 2000, 9 INT C INF DIS BUEN, P113
[9]   Absence of specific mucosal antibody responses in HIV-exposed uninfected sex workers from the Gambia [J].
Dorrell, L ;
Hessell, AJ ;
Wang, M ;
Whittle, H ;
Sabally, S ;
Rowland-Jones, S ;
Burton, DR ;
Parren, PWHI .
AIDS, 2000, 14 (09) :1117-1122
[10]  
FERRARI G, 1995, CLIN EXP IMMUNOL, V101, P239