Interferon-α generation and immune reconstitution during antiretroviral therapy for human immunodeficiency virus infection

被引:82
作者
Siegal, FP
Fitzgerald-Bocarsly, P
Holland, BK
Shodell, M
机构
[1] St Vincents Catholic Med Ctr New York, Dept Med, Sect HIV Med, New Hyde Pk, NY USA
[2] Long Isl Jewish Med Ctr AECOM, Div Hematol Oncol, New Hyde Pk, NY 11042 USA
[3] Long Isl Jewish Med Ctr AECOM, Dept Allergy & Clin Immunol, New Hyde Pk, NY 11042 USA
[4] Univ Med & Dent New Jersey, New Jersey Med Sch, Div Biostat & Epidemiol, Dept Pathol & Lab Med, Newark, NJ 07103 USA
[5] Univ Med & Dent New Jersey, New Jersey Med Sch, Div Biostat & Epidemiol, Dept Prevent Med, Newark, NJ 07103 USA
[6] Long Isl Univ, Dept Biol, Brookville, NY USA
关键词
dendritic cells; Th1; cellular immunity; natural immunity; immunocompromised host; plasmacytoid; interferons; T cells; interferon-alpha; HIV; AIDS; natural interferon-producing cell;
D O I
10.1097/00002030-200109070-00002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: To quantify the effect of HIV infection and HIV-suppressive therapy on interferon-alpha (IFN-alpha) production by human blood mononuclear cells; to compare, in parallel, effects on CD4+ T-cell numbers; and to ascertain the relationship of these interferon and CD4 parameters to resistance to opportunistic infections. Design: Serial studies of 294 unselected patients with HIV infection during therapy, with outcomes analysis. Methods: Determination of IFN generation by blood mononuclear cells via bioassay, and T-lymphocyte subset analysis via flow cytometry; serial studies of individual patients; linear regression and chi (2) contingency table analysis. Results: HIV burden is inversely related to interferon-alpha generation, much as it is to CD4+ T-cell counts. Both of these recover during HIV-suppressive therapy. Reconstitution of IFN-alpha generation to levels commensurate with protection against opportunistic infection occurs prior to similar restoration of CD4 counts. In the outcomes analyses, such immune reconstitution was associated with protection from recurrent or new opportunistic infection. Conversely, viral suppression without such immunologic recovery was not protective against opportunistic infection. Conclusions: Rapidly responding IFN-alpha generating cells appear to participate in resistance to opportunistic intracellular infection. Recovery of IFN-alpha generation may be an early marker of immune reconstitution in AIDS. (C) 2001 Lippincott Williams & Wilkins
引用
收藏
页码:1603 / 1612
页数:10
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