Normalized CD8+ but not CD4+ lymphocyte IL-2 expression is associated with early treatment with highly active antiretroviral therapy

被引:6
作者
Akerele, Toks [1 ]
Galatowicz, Grazyna [1 ]
Bunce, Catey [1 ]
Calder, Virginia [1 ]
Lynn, William A. [1 ]
Lightman, Susan [1 ]
机构
[1] Moorfields Eye Hosp, Inst Ophthalmol, London EC1V 2PD, England
关键词
HIV; HAART; CD8+T cells; cytokines; interferon gamma;
D O I
10.1016/j.clim.2006.07.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4+ and CD8+ lymphocyte cytokine production in patients with HIV/AIDS and Controls, in response to stimulation with phorbol-12-myristate-13-acetate (PMA) and ionomycin was assessed using single cell flow cytometric methods. Sixty-eight patients with HIV were divided into those on no antiretroviral therapy and those on highly active antiretroviral therapy (HAART). Patients on HAART were analyzed further on the basis of gender, ethnicity, viral load (> or <= 50 copies/ml), CD4 count change from nadir (> 100 or < 100 cells/mm(3)) and CD4 count (> 200 or < 200 cells/mm(3)). Interferon gamma (IFN gamma) expression by CD4+ and CD8+ lymphocytes was elevated in HIV-infected groups as compared to Controls. This elevation was statistically significant for patients on HAART but not for those not on HAART. The most significant difference was seen when the CD4+ count reached > 200 cells/mm(3) (p=0.018 for CD4+ IFN gamma production and p=0.004 for CD8+ IFN gamma production). CD4+ interleukin-2 (IL-2) expression was significantly lower in HIV patients as compared to Controls but did not significantly improve however good the response to HAART. IL-2 expression by CD8+ lymphocytes was also lower in HIV patients as compared to Controls. IL-2 expression by CD8+ lymphocytes significantly improved in all. patients on HAART as compared to HIV patients on no HAART. IL-2 expression was not significantly different from that of the Controls when the HIV viral toad was less than 50 copies/ml. These results demonstrate improvements in both CD4+ and CD8+ responsiveness with HAART. IFN gamma production was elevated in response to HAART and was maximal. only with significant CD4 count recovery. In contrast, normalization of IL-2 production by CD8+ lymphocytes was seen early in patients receiving HAART even when there was only a small increase in CD4+ lymphocyte numbers. (c) 2006 Published by Elsevier Inc.
引用
收藏
页码:191 / 197
页数:7
相关论文
共 38 条
[1]  
Altfeld M, 2000, J ACQ IMMUN DEF SYND, V23, P287
[2]   Positive effects of combined antiretroviral therapy on CD4(+) T cell homeostasis and function in advanced HIV disease [J].
Autran, B ;
Carcelain, G ;
Li, TS ;
Blanc, C ;
Mathez, D ;
Tubiana, R ;
Katlama, C ;
Debre, P ;
Leibowitch, J .
SCIENCE, 1997, 277 (5322) :112-116
[3]  
Bailer RT, 1999, J IMMUNOL, V162, P7534
[4]  
Bernard I, 1998, EUR CYTOKINE NETW, V9, P613
[5]   Decreases in plasma TNF-α level and IFN-γ mRNA level in peripheral blood mononuclear cells (PBMC) and an increase in IL-2 mRNA level in PBMC are associated with effective highly active antiretroviral therapy in HIV-infected patients [J].
Brazille, P ;
Dereuddre-Bosquet, N ;
Leport, C ;
Clayette, P ;
Boyer, O ;
Vildé, JL ;
Dormont, D ;
Benveniste, O .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2003, 131 (02) :304-311
[6]   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
[7]   T cell changes after combined nucleoside analogue therapy in HIV primary infection [J].
Carcelain, G ;
Blanc, C ;
Leibowitch, J ;
Mariot, P ;
Mathez, D ;
Schneider, V ;
Saimot, AG ;
Damond, F ;
Simon, F ;
Debré, P ;
Autran, B ;
Girard, PM .
AIDS, 1999, 13 (09) :1077-1081
[8]   CD28 costimulation and CD28 expression in T lymphocyte subsets in HIV-1 infection with and without progression to AIDS [J].
Choremi-Papadopoulou, H ;
Panagiotou, N ;
Samouilidou, E ;
Kontopidou, F ;
Viglis, V ;
Antoniadou, A ;
Kosmidis, J ;
Kordossis, T .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2000, 119 (03) :499-506
[9]   A T(H)1-]T(H)2 SWITCH IS A CRITICAL STEP IN THE ETIOLOGY OF HIV-INFECTION [J].
CLERICI, M ;
SHEARER, GM .
IMMUNOLOGY TODAY, 1993, 14 (03) :107-110
[10]   Effects of subcutaneous interleukin-2 therapy on CD4 subsets and in vitro cytokine production in HIV plus subjects [J].
De Paoli, P ;
Zanussi, S ;
Simonelli, C ;
Bortolin, MT ;
D'Andrea, M ;
Crepaldi, C ;
Talamini, R ;
Comar, M ;
Giacca, M ;
Tirelli, U .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (11) :2737-2743