Biomarkers of CD4+ T-cell activation as risk factors for tuberculosis-associated immune reconstitution inflammatory syndrome

被引:29
|
作者
Chakrabarti, Lisa A. [1 ]
Boucherie, Celine [2 ,3 ]
Bugault, Florence [4 ]
Cumont, Marie-Christine [4 ]
Roussillon, Caroline [2 ,3 ]
Breton, Guillaume [5 ]
Patey, Olivier [6 ]
Chene, Genevieve [2 ,3 ,7 ]
Richert, Laura [2 ,3 ]
Lortholary, Olivier [8 ]
机构
[1] Inst Pasteur, INSERM, U1108, Unite Pathogenie Virale, F-75724 Paris 15, France
[2] Univ Bordeaux, ISPED, Bordeaux, France
[3] INSERM ISPED, Ctr INSERM, Epidemiol Biostat U897, Bordeaux, France
[4] Inst Pasteur, Unite Immunol Cellulaire, F-75724 Paris 15, France
[5] Hop La Pitie Salpetriere, Serv Med Interne, Paris, France
[6] Hop Villeneuve St Georges, Villeneuve St Georges, France
[7] CHU Bordeaux, Pole Sante Publ, Serv Informat Med, Bordeaux, France
[8] Univ Paris 05, Hop Necker Enfants Malad, APHP, Paris, France
关键词
biomarker; HIV; immune reconstitution inflammatory syndrome; interleukin-7; soluble interleukin-2 receptor; tuberculosis; HIV-INFECTED PATIENTS; ANTIRETROVIRAL THERAPY; RESTORATION DISEASE; HIV-1-INFECTED PATIENTS; RESPONSES; IL-7; MENINGITIS; CYTOKINE; RECEPTOR; IMMUNOPATHOGENESIS;
D O I
10.1097/QAD.0000000000000311
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: Patients coinfected with HIV and Mycobacterium tuberculosis frequently experience a paradoxical worsening of tuberculosis (TB) symptoms early after the initiation of combination antiretroviral therapy (cART). This immune reconstitution inflammatory syndrome (TB-IRIS) can lead to significant morbidity and needs to be distinguished from TB recurrence due to ineffective treatment. We investigated whether plasma biomarkers could predict the occurrence of TB-IRIS. Design: ANRS 129 BKVIR is a single-arm multicentre trial that enrolled 69 cART-naive HIV-1-infected patients treated for TB. The patients received once-daily tenofovir/emtricitabine/efavirenz first-line regimen. TB-IRIS cases (IRIS+) were validated by an Event Review Committee. Methods: A panel of 26 plasma biomarkers was monitored longitudinally for 24 weeks from cART initiation onward, using multiplexed assays and high-sensitivity ELISA. Statistical analyses of biomarkers were adjusted for test multiplicity. Results: One-third of patients (n = 23) experienced TB-IRIS. The inflammatory cytokines and chemokines interleukin (IL)-6, IL-8, interferon-gamma-induced protein 10 (IP-10), and tumour necrosis factor-alpha (TNF-alpha) showed increased plasma levels at week 4 in IRIS-positive (IRIS+) patients (P < 0.05 for each biomarker). The soluble IL-2 receptor sCD25, which is released upon CD4(+) T-cell activation, was significantly increased at week 0 in IRIS+ patients (P< 0.05), and remained elevated throughout follow-up. IL-7, a key homeostatic cytokine for CD4(+) T-cells, showed a trend for higher values in the TB-IRIS group. Both sCD25 and IL-7 baseline levels were independently associated with a shorter time to TB-IRIS occurrence (P = 0.005 and P = 0.02, respectively). Conclusion: These findings support a role for CD4(+) T-cell activation prior to massive inflammation in the development of TB-IRIS. (C) 2014 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
引用
收藏
页码:1593 / 1602
页数:10
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