Explosion of tuberculin-specific Th1-responses induces immune restoration syndrome in tuberculosis and HIV co-infected patients

被引:234
作者
Bourgarit, A
Carcelain, G
Martinez, V
Lascoux, C
Delcey, V
Gicquel, B
Vicaut, E
Lagrange, PH
Sereni, D
Autran, B
机构
[1] Univ Paris 06, Pitie Salpetriere Hosp, Cellular Immunol Lab, Paris, France
[2] Hop St Louis, Dept Internal Med, Paris, France
[3] Lariboisiere Hosp, Dept Internal Med, Paris, France
[4] Inst Pasteur, Mycobacterial Genet Unit, Paris, France
[5] Hop Fernand Widal, Clin Res Unit, Paris, France
[6] Hop St Louis, Microbiol Lab, Paris, France
关键词
immune restoration syndrome; HIV-1; tuberculosis; HAART; ESAT-6; PPD;
D O I
10.1097/01.aids.0000202648.18526.bf
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 test the hypothesis that an acute exacerbation of mycobacteria-specific Th1 response after HIV infection control by HAART Causes immune restoration syndrome (IRS) in HIV-tuberculosis (TB) coinfected patients. Design: Prospective, multicenter Study of 19 consecutive untreated HIV-TB coinfected patients included when initiating antimycobacterial therapy and sequentially evaluated during HAART and at time of IRS. IRS was defined according to classical clinical diagnostic criteria. Patients were declared IRS- if no IRS occurred within 3 months after HAART initiation. Methods: Mycobacteria-specific [purified protein derivative (PPD), ESAT-6, 85131 Th1 cells producing interferon (IFN)-gamma quantified by ELISpot, in vitro production of 25 cytokines/chemokines in antigen-stimulated peripheral blood mononuclear cell (PBMC) supernatants quantified by chemiluminescence. Results: Seven patients (37%) experienced IRS (IRS+). Mycobacteria-specific (PPD) Th1 IFN-gamma-producing cells increased sharply during IRS (median, 2970 spot forming cells/10(6) PBMC), but not the cytomegalovirus-specific responses tested as control. Only three IRS+ patients had low ESAT-6- but no 85B-specific responses. IRS- patients did not develop acute PPD-specific responses except in one case. In addition, at time of IRS a peak of PPD-specific Th1 cytokines/chemokines [interleukin (IL)-2, IL-12, IFN-gamma, IP10 and monokine-induced by IFN-gamma] without Th2 cytokines, and a peak of non-specific inflammatory cytokines/chemokines (TNF-alpha, IL-6, IL-1 beta, IL-10, RANTES and MCP-1) occurred. These findings were independent from CD4 cell Count, viral loads or time of HAART initiation. Conclusion: An acute exacerbation of Th1 responses against mycobacterial antigens appears to cause IRS in patients co-infected with HIV and TB. This key event provides new evidence valuable for the diagnosis and treatment of IRS. (C) 2006 Lippincott Williams & Wilkins.
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页码:F1 / F7
页数:7
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