RECONSTITUTION OF LONG-TERM T-HELPER CELL-FUNCTION AFTER ZIDOVUDINE THERAPY IN HUMAN IMMUNODEFICIENCY VIRUS-INFECTED PATIENTS

被引:40
作者
CLERICI, M
LANDAY, AL
KESSLER, HA
PHAIR, JP
VENZON, DJ
HENDRIX, CW
LUCEY, DR
SHEARER, GM
机构
[1] NCI,CLIN ONCOL PROGRAM,BETHESDA,MD 20892
[2] RUSH PRESBYTERIAN ST LUKES MED CTR,DEPT IMMUNOL MICROBIOL,CHICAGO,IL 60612
[3] RUSH PRESBYTERIAN ST LUKES MED CTR,DEPT MED,CHICAGO,IL 60612
[4] NORTHWESTERN UNIV,SCH MED,DEPT MED,CHICAGO,IL 60611
[5] WILFORD HALL USAF MED CTR,HIV UNIT,LACKLAND AFB,TX 78236
基金
美国国家卫生研究院;
关键词
D O I
10.1093/infdis/166.4.723
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Peripheral blood mononuclear cells from 12 asymptomatic patients infected with human immunodeficiency virus (HIV) and 4 patients with AIDS were analyzed before and during therapy with zidovudine for T helper cell (Th) function. Th function improved by more than fourfold to one or more of three stimuli tested in 9 (75%) of 12 asymptomatic patients on zidovudine therapy and in 3 of 4 patients with AIDS. Only 6 (7.4%) of 80 untreated HIV-infected control patients showed spontaneous improvement in Th function (P < 10(-6)). Improved Th function was detected as early as 5 weeks into therapy in 6 patients and continued to be evident for > 1 year after start of therapy in 6 patients and for > 2 years in 2 patients. No correlation was observed between improved Th function and changes in CD4+ or CD8+ cell numbers or in levels of serum HIV p24 antigen or beta2-microglobulin. These results suggest inclusion of in vitro Th function as a useful marker in determining the efficacy of antiretroviral drug therapy of HIV-infected patients.
引用
收藏
页码:723 / 730
页数:8
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