Identification of a reservoir for HIV-1 in patients on highly active antiretroviral therapy

被引:2541
作者
Finzi, D
Hermankova, M
Pierson, T
Carruth, LM
Buck, C
Chaisson, RE
Quinn, TC
Chadwick, K
Margolick, J
Brookmeyer, R
Gallant, J
Markowitz, M
Ho, DD
Richman, DD
Siliciano, RF
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT MED,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH HYG & PUBL HLTH,DEPT MOL MICROBIOL & IMMUNOL,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH HYG & PUBL HLTH,DEPT BIOSTAT,BALTIMORE,MD 21205
[4] AARON DIAMOND AIDS RES CTR,NEW YORK,NY 10016
[5] UNIV CALIF SAN DIEGO,DEPT MED,LA JOLLA,CA 92093
[6] UNIV CALIF SAN DIEGO,DEPT PATHOL,LA JOLLA,CA 92093
关键词
D O I
10.1126/science.278.5341.1295
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The hypothesis that quiescent CD4(+) T lymphocytes carrying proviral DNA provide a reservoir for human immunodeficiency virus-type 1 (HIV-1) in patients on highly active antiretroviral therapy (HAART) was examined. In a study of 22 patients successfully treated with HAART for up to 30 months, replication-competent virus was routinely recovered from resting CD4(+) T lymphocytes. The frequency of resting CD4(+) T cells harboring talent HIV-l was low, 0.2 to 16.4 per 10(6) cells, and, in cross-sectional analysis, did not decrease with increasing time on therapy. The recovered viruses generally did not show mutations associated with resistance to the relevant antiretroviral drugs. This reservoir of nonevolving latent virus in resting CD4(+) T cells should be considered in deciding whether to terminate treatment in patients who respond to HAART.
引用
收藏
页码:1295 / 1300
页数:6
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