Effect of baseline- and treatment-related factors on immunologic recovery after initiation of antiretroviral therapy in HIV-1-positive subjects: Results from ACTG 384

被引:138
作者
Gandhi, Rajesh T.
Spritzler, John
Chan, Ellen
Asmuth, David M.
Rodriguez, Benigno
Merigan, Thomas C.
Hirsch, Martin S.
Shafer, Robert W.
Robbins, Gregory K.
Pollard, Richard B.
机构
[1] Massachusetts Gen Hosp, Infect Dis Unit, Boston, MA 02114 USA
[2] Harvard Univ, Sch Publ Hlth, Cambridge, MA 02138 USA
[3] Univ Calif Davis, Med Ctr, Davis, CA 95616 USA
[4] Case Western Reserve Univ, Sch Med, Cleveland, OH 44106 USA
[5] Stanford Univ, Med Ctr, Stanford, CA 94305 USA
关键词
HIV-1; antiretroviral therapy; immunologic outcomes; CD4 cell recovery; T-cell activation; memory and naive CD4 cell subsets;
D O I
10.1097/01.qai.0000226789.51992.3f
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To assess the effect of baseline- and treatment-related factors on immunologic recovery after initiation of antiretroviral therapy (ART). Methods: Nine hundred eighty antiretroviral-naive HIV-1+ subjects were randomized to start stavudine/didanosine or zidovudine/lamivudine with nelfinavir, efavirenz, or both nelfinavir and efavirenz. Results: Greater CD4 cell recovery was associated with age of 40 years or younger, female sex, higher baseline naive/memory CD4 cell ratio, higher baseline virus load (VL), and virologic suppression (VS). Most subjects who maintained an undetectable VL had a substantial increase in CD4 cell count, but 13% of the subjects did not, even after 3 years of VS. Persistent T-cell activation was associated with lower CD4 cell recovery, even in subjects who achieved VS. Initial treatment assignment did not affect total CD4 cell recovery, naive/memory CD4 cell reconstitution, or decline in T-cell activation. In addition to CD4 cell recovery, B-cell counts rose substantially after ART initiation. Conclusions: In this large randomized trial, younger age, female sex, higher naive/memory CD4 cell ratio, higher baseline VL, and VS were associated with greater CD4 cell increase, whereas per sistent T-cell activation was associated with impaired CD4 cell recovery after ART initiation. Initial treatment assignment did not affect CD4 cell reconstitution.
引用
收藏
页码:426 / 434
页数:9
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