Immunological and virological responses in HIV-1-infected adults at early stage of established infection treated with highly active antiretroviral therapy

被引:58
作者
Bart, PA
Rizzardi, GP
Tambussi, G
Chave, JP
Chapuis, AG
Graziois, C
Corpataux, JM
Halkic, N
Meuwly, JY
Munoz, M
Meylan, P
Spreen, W
McDade, H
Yerly, S
Perrin, L
Lazzarin, A
Pantaleo, G
机构
[1] Univ Lausanne, CHU Vaudois, Dept Med, Div Infect Dis,Lab AIDS Immunopathogenesis, CH-1011 Lausanne, Switzerland
[2] Univ Lausanne, CHU Vaudois, Dept Gen Surg, CH-1011 Lausanne, Switzerland
[3] Univ Lausanne, CHU Vaudois, Dept Radiol, CH-1011 Lausanne, Switzerland
[4] Univ Lausanne, CHU Vaudois, Inst Microbiol, CH-1011 Lausanne, Switzerland
[5] Ist Sci San Raffaele, Div Infect Dis, I-20127 Milan, Italy
[6] Clin Source, CH-1004 Lausanne, Switzerland
[7] GlaxoWellcome, Res Triangle Pk, NC 27709 USA
[8] GlaxoWellcome, Greenford UB6 0HE, Middx, England
[9] Univ Geneva, Cent Lab Virol, CH-1211 Geneva, Switzerland
关键词
early established infection; HAART; HIV; HIV-specific CD4 cell responses; immune reconstitution; lymph node; plasma viraemia;
D O I
10.1097/00002030-200009080-00002
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 evaluate the immunological and virological responses ro highly active antiretroviral therapy (HAART) in blood and lymphoid compartments of HIV-1-infected patients at an early stage of infection. Design: An open-label, observational, non-randomized, prospective trial of outpatients attending the Centre of Clinical Investigation in Infectious Diseases, Centre Hospitalier Universitaire Vaudois, University of Lausanne, Switzerland. Subjects: Forty-one antiretroviral-naive HIV-l-infected adults with 400 CD4 T cells/mu l or greater and 5000 plasma HIV-1-RNA copies/ml or greater were enrolled, and 32 finished the study. Forty-nine HIV-negative individuals were included as controls. All subjects gave written informed consent. Interventions: All patients received abacavir 300 mg by mouth every 12 h and amprenavir 1200 mg by mouth every 12 h for 72 weeks. Mainoutcome measures: The extent of immune reconstitution in blood and lymph nodes after 72 weeks of HAART was evaluated, and compared with immunological measures of 49 HIV-negative subjects. Results: Virus replication was effectively suppressed (-3.5 log(10) at week 72). Substantial increments of CD4 T cell count in blood and percentage in lymph nodes were observed over time, and these measures were comparable to HIV-negative subjects by week 24 in blood and by week 48 in lymph nodes. The increase was equally distributed between naive and memory CD4 T cells. Recovery of HIV-specific CD4 responses occurred in 40% of patients. Conclusion: The initiation of HAART at an early stage of established HIV infection induces systemic quantitative normalization of CD4 T cells, a partial recovery of HIV-specific CD4 cell responses, and effective and durable suppression of virus replication. (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码:1887 / 1897
页数:11
相关论文
共 45 条
[11]   Nucleoside analog 1592U89 and human immunodeficiency virus protease inhibitor 141W94 are synergistic in vitro [J].
Drusano, GL ;
D'Argenio, DZ ;
Symonds, W ;
Bilello, PA ;
McDowell, J ;
Sadler, B ;
Bye, A ;
Bilello, JA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (09) :2153-2159
[12]   Unique intracellular activation of the potent anti-human immunodeficiency virus agent 1592U89 [J].
Faletto, MB ;
Miller, WH ;
Garvey, EP ;
Clair, MHS ;
Daluge, SM ;
Good, SS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (05) :1099-1107
[13]   Viral dynamics in HIV-1 infection [J].
Finzi, D ;
Siliciano, RF .
CELL, 1998, 93 (05) :665-671
[14]   Latent infection of CD4+ T cells provides a mechanism for lifelong persistence of HIV-1, even in patients on effective combination therapy [J].
Finzi, D ;
Blankson, J ;
Siliciano, JD ;
Margolick, JB ;
Chadwick, K ;
Pierson, T ;
Smith, K ;
Lisziewicz, J ;
Lori, F ;
Flexner, C ;
Quinn, TC ;
Chaisson, RE ;
Rosenberg, E ;
Walker, B ;
Gange, S ;
Gallant, J ;
Siliciano, RF .
NATURE MEDICINE, 1999, 5 (05) :512-517
[15]   Identification of a reservoir for HIV-1 in patients on highly active antiretroviral therapy [J].
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 .
SCIENCE, 1997, 278 (5341) :1295-1300
[16]   Limited CD4+ T-cell renewal in early HIV-1 infection:: Effect of highly active antiretroviral therapy [J].
Fleury, S ;
de Boer, RJ ;
Rizzardi, GP ;
Wolthers, KC ;
Otto, SA ;
Welbon, CC ;
Graziosi, C ;
Knabenhans, C ;
Soudeyns, H ;
Bart, PA ;
Gallant, S ;
Corpataux, JM ;
Gillet, M ;
Meylan, P ;
Schnyder, P ;
Meuwly, JY ;
Spreen, W ;
Glauser, MP ;
Miedema, F ;
Pantaleo, G .
NATURE MEDICINE, 1998, 4 (07) :794-801
[17]   HIV-protease inhibitors [J].
Flexner, C .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (18) :1281-1292
[18]   Abacavir [J].
Foster, RH ;
Faulds, D .
DRUGS, 1998, 55 (05) :729-736
[19]   Persistence of HIV-1 transcription in peripheral-blood mononuclear cells in patients receiving potent antiretroviral therapy [J].
Furtado, MR ;
Callaway, DS ;
Phair, JP ;
Kunstman, KJ ;
Stanton, JL ;
Macken, CA ;
Perelson, AS ;
Wolinsky, SM .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (21) :1614-1622
[20]   Treatment with indinavir, zidovudine, and lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy [J].
Gulick, RM ;
Mellors, JW ;
Havlir, D ;
Eron, JJ ;
Gonzalez, C ;
McMahon, D ;
Richman, DD ;
Valentine, FT ;
Jonas, L ;
Meibohm, A ;
Emini, EA ;
Chodakewitz, JA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (11) :734-739