T cell activation is associated with lower CD4+ T cell gains in human immunodeficiency virus-infected patients with sustained viral suppression during antiretroviral therapy

被引:696
作者
Hunt, PW
Martin, JN
Sinclair, E
Bredt, B
Hagos, E
Lampiris, H
Deeks, SG
机构
[1] Vet Affairs Med Ctr, GIM Sect 111A1, San Francisco, CA 94121 USA
[2] San Francisco Gen Hosp, Dept Med, Posit Hlth Program, San Francisco, CA 94110 USA
[3] San Francisco Gen Hosp, Dept Med, Gen Clin Res Ctr, San Francisco, CA 94110 USA
[4] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Ctr AIDS Prevent Studies, San Francisco, CA 94143 USA
关键词
D O I
10.1086/374786
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 T cell activation is associated with disease progression in untreated human immunodeficiency virus type 1 ( HIV-1) infection, its significance in antiretroviral- treated patients is unknown. Activated ( CD38(+) HLA-DR+) T cell counts were measured in 99 HIV-infected adults who had maintained a plasma HIV RNA level less than or equal to1000 copies/mL for a median of 21 months while receiving antiretroviral therapy. Patients with sustained viral suppression had lower levels of T cell activation than untreated patients but higher levels than HIV-uninfected control subjects. Persistent T cell activation was associated with decreased CD4(+) T cell gains during therapy. For every 5% increase in the proportion of activated CD8(+) T cells, 35 fewer CD4(+) T cells/ mm(3) were gained. Increased T cell activation was associated with shorter duration of viral suppression, hepatitis C virus coinfection, frequent low-level viremia, and lower nadir CD4(+) T cell counts. Interventions that directly target T cell activation or the determinants of activation may prove to be useful adjuvants to antiretroviral therapy.
引用
收藏
页码:1534 / 1543
页数:10
相关论文
共 60 条
[1]  
*AIDS, 2002, DEP HLTH HUM SERV KA
[2]  
AMEISEN JC, 1991, IMMUNOL TODAY, V12, P102
[3]   REGULATION OF HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION - IMPLICATIONS FOR PATHOGENESIS [J].
ANTONI, BA ;
STEIN, SB ;
RABSON, AB .
ADVANCES IN VIRUS RESEARCH, VOL 43, 1994, 43 :53-145
[4]  
ASCHER MS, 1988, CLIN EXP IMMUNOL, V73, P165
[5]   The HIV coreceptors CXCR4 and CCR5 are differentially expressed and regulated on human T lymphocytes [J].
Bleul, CC ;
Wu, LJ ;
Hoxie, JA ;
Springer, TA ;
Mackay, CR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) :1925-1930
[6]   Increased numbers of primed activated CD8+CD38+CD45RO+ T cells predict the decline of CD4+ T cells in HIV-1-infected patients [J].
Bofill, M ;
Mocroft, A ;
Lipman, M ;
Medina, E ;
Borthwick, NJ ;
Sabin, CA ;
Timms, A ;
Winter, M ;
Baptista, L ;
Johnson, MA ;
Lee, CA ;
Phillips, AN ;
Janossy, G .
AIDS, 1996, 10 (08) :827-834
[7]   Initial increase in blood CD4+ lymphocytes after HIV antiretroviral therapy reflects redistribution from lymphoid tissues [J].
Bucy, RP ;
Hockett, RD ;
Derdeyn, CA ;
Saag, MS ;
Squires, K ;
Sillers, M ;
Mitsuyasu, RT ;
Kilby, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (10) :1391-1398
[8]  
Calabrese LH, 2002, J ACQ IMMUN DEF SYND, V29, P356, DOI 10.1097/00126334-200204010-00005
[9]  
Capobianchi MR, 1996, J BIOL REG HOMEOS AG, V10, P83
[10]   Increased levels of activated subsets of CD4 T cells add to the prognostic value of low CD4 T cell counts in a cohort of HIV-infected drug users [J].
Carbone, J ;
Gil, J ;
Benito, JM ;
Navarro, J ;
Muñóz-Fernández, A ;
Bartolomé, J ;
Zabay, JM ;
López, F ;
Fernández-Cruz, E .
AIDS, 2000, 14 (18) :2823-2829