Reconstitution of immune responses to tuberculosis in patients with HIV infection who receive antiretroviral therapy

被引:75
|
作者
Schluger, NW [1 ]
Perez, D [1 ]
Liu, YM [1 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Div Pulm Allergy & Crit Care Med, Dept Med, New York, NY 10032 USA
关键词
AIDS; immunity; treatment; tuberculosis;
D O I
10.1378/chest.122.2.597
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Study objectives: To assess the restoration of immune responses to tuberculosis, as manifested by secretion of T-helper type 1 cytokines (interferon [IFN]-gamma, interleukin [IL]-12, and IL-2) ana T-helper type 2 cytokines (IL-10), in HIV-positive patients who receive antiretroviral therapy (ART). Design: Prospective cohort study. Setting: University hospital. Patients: Ten HIV-positive patients, all naive to ART and all about to start ART for clinical indications, and 11 healthy, HIV-negative control subjects. Interventions: Assessment of T-cell proliferation and cytokine production after administration of ART to patients with HIV infection. Measurements and results: All patients had a negative tuberculin skin test result at baseline and were anergic. Highly active ART reduced the viral load to very low levels in all patients within a short time after starting therapy. Blood samples were drawn every 2 months after starting therapy, and continued for 1 year while the patients continued to receive ART. There were trends toward increased proliferation of peripheral blood mononuclear cells (PBMCs) in response to Mycobacterium tuberculosis-specific stimuli, but these were delayed until several months of ART had elapsed. Similar trends were noted in relation to the secretion of IFN-gamma. Neither PBMC proliferation nor IFN-gamma secretion reached levels seen in healthy control subjects. No consistent trends in IL-2, IL-10, or IL-12 production were noted. Conclusion: ART restores immune responses to M tuberculosis, although this restoration is delayed and does not reach levels seen in healthy, HIV-negative control subjects. These results may explain in part the phenomenon of paradoxic reactions to antituberculosis therapy in patients with HIV infection. A larger study in which patients are followed up for a longer period of time will allow the magnitude and timing of this reconstitution to be more precisely, defined.
引用
收藏
页码:597 / 602
页数:6
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