Restoration of normal interleukin-2 production by CD4+ T cells of human immunodeficiency virus-infected patients after 9 months of highly active antiretroviral therapy
被引:40
作者:
Weiss, L
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机构:Hop Broussais, INSERM, U430, F-75014 Paris, France
Weiss, L
Ancuta, P
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机构:Hop Broussais, INSERM, U430, F-75014 Paris, France
Ancuta, P
Girard, PM
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机构:Hop Broussais, INSERM, U430, F-75014 Paris, France
Girard, PM
Bouhlal, H
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机构:Hop Broussais, INSERM, U430, F-75014 Paris, France
Bouhlal, H
Roux, A
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机构:Hop Broussais, INSERM, U430, F-75014 Paris, France
Roux, A
Cavaillon, NH
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机构:Hop Broussais, INSERM, U430, F-75014 Paris, France
Cavaillon, NH
Kazatchkine, MD
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机构:Hop Broussais, INSERM, U430, F-75014 Paris, France
Kazatchkine, MD
机构:
[1] Hop Broussais, INSERM, U430, F-75014 Paris, France
[2] Univ Paris 06, Hop Broussais, F-75014 Paris, France
[3] Hop Rothschild, Serv Malad Infect, F-75571 Paris, France
The present study investigated immune restoration in patients at intermediate stages of human immunodeficiency virus (HIV) disease after initiation of highly active antiretroviral therapy (HAART). A progressive increase in both memory and naive CD4(+) T cells was observed from the first weeks of therapy, concomitant with a decrease in the expression of activation markers on CD8(+) T cells. The early-activation marker CD69 remained, however, overexpressed on T cells after suboptimal stimulation in vitro, indicative of persistent immune activation. The percentage of interleukin (IL)-2-producing CD4(+) T cells significantly increased from 9 months of HAART In most patients, CD4(+) T cells recovered an ability to produce IL-2 on stimulation, similar to that of HIV-seronegative controls. Reversal of T-cell anergy may be a key event in immune restoration for achieving long-term clinical benefit with HAART.