HIV-1 actively replicates in naive CD4+ T cells residing within human lymphoid tissues

被引:199
作者
Eckstein, DA
Penn, ML
Korin, YD
Scripture-Adams, DD
Zack, JA
Kreisberg, JF
Roederer, M
Sherman, MP
Chin, PS
Goldsmith, MA [1 ]
机构
[1] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94141 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94141 USA
[3] Univ Calif San Francisco, Sch Med, San Francisco, CA 94141 USA
[4] Univ Calif Los Angeles, Dept Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Sch Med, Dept Microbiol & Mol Genet, Los Angeles, CA 90095 USA
[6] NIH, Vaccine Res Ctr, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S1074-7613(01)00217-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although HIV-1 gene expression is detected in naive, resting T cells in vivo, such cells are resistant to productive infection in vitro. However, we found that the endogenous. microenvironment of human lymphoid tissues supports de novo infection and depletion of this population. Cell cycle analysis and DNA labeling experiments established that these cells were definitively quiescent and thus infected de novo. Quantitation of the "burst size" within naive cells further demonstrated that these cells were productively infected and contributed to the local viral burden. These findings demonstrate that lymphoid tissues support active HIV-1 replication in resting, naive T cells. Moreover, these cells are not solely reservoirs of latent virus but are permissive hosts for viral replication that likely targets them for elimination.
引用
收藏
页码:671 / 682
页数:12
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