Interferon-Gamma Release Assays for the Diagnosis of Latent Tuberculosis Infection in HIV-Infected Individuals: A Systematic Review and Meta-Analysis

被引:230
作者
Cattamanchi, Adithya [1 ,2 ]
Smith, Rachel [1 ]
Steingart, Karen R. [2 ]
Metcalfe, John Z. [1 ,2 ]
Date, Anand [3 ]
Coleman, Courtney [3 ]
Marston, Barbara J. [3 ]
Huang, Laurence [1 ,4 ]
Hopewell, Philip C. [1 ,2 ]
Pai, Madhukar [5 ]
机构
[1] Univ Calif San Francisco, San Francisco Gen Hosp, Div Pulm & Crit Care Med, San Francisco, CA USA
[2] Univ Calif San Francisco, Curry Int TB Ctr, San Francisco, CA 94143 USA
[3] Ctr Dis Control & Prevent, Div Global HIV AIDS, Atlanta, GA USA
[4] Univ Calif San Francisco, San Francisco Gen Hosp, Div HIV AIDS, San Francisco, CA USA
[5] McGill Univ, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ H3A 1A2, Canada
基金
美国国家卫生研究院;
关键词
latent tuberculosis infection; systematic review; interferon-gamma release assay; HIV infection; tuberculin skin test; CELL-BASED ASSAYS; GOLD IN-TUBE; SKIN-TEST; IMMUNODIAGNOSIS; PERFORMANCE; PREVALENCE; UTILITY; ADULTS; TESTS; RISK;
D O I
10.1097/QAI.0b013e31820b07ab
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: To determine whether interferon-gamma release assays (IGRAs) improve the identification of HIV-infected individuals who could benefit from latent tuberculosis infection therapy. Design: Systematic review and meta-analysis. Methods: We searched multiple databases through May 2010 for studies evaluating the performance of the newest commercial IGRAs (QuantiFERON-TB Gold In-Tube [QFT-GIT] and T-SPOT. TB [TSPOT]) in HIV-infected individuals. We assessed the quality of all studies included in the review, summarized results in prespecified subgroups using forest plots, and where appropriate, calculated pooled estimates using random effects models. Results: The search identified 37 studies that included 5736 HIV-infected individuals. In three longitudinal studies, the risk of active tuberculosis was higher in HIV-infected individuals with positive versus negative IGRA results. However, the risk difference was not statistically significant in the two studies that reported IGRA results according to manufacturer-recommended criteria. In persons with active tuberculosis (a surrogate reference standard for latent tuberculosis infection), pooled sensitivity estimates were heterogeneous but higher for TSPOT (72%; 95% confidence interval [CI], 62-81%) than for QFT-GIT (61%; 95% CI, 47-75%) in low-/middle-income countries. However, neither IGRA was consistently more sensitive than the tuberculin skin test in head-to-head comparisons. Although TSPOT appeared to be less affected by immunosuppression than QFT-GIT and the tuberculin skin test, overall, differences among the three tests were small or in conclusive. Conclusions: Current evidence suggests that IGRAs perform similarly to the tuberculin skin test at identifying HIV-infected individuals with latent tuberculosis infection. Given that both tests have modest predictive value and suboptimal sensitivity, the decision to use either test should be based on country guidelines and resource and logistic considerations.
引用
收藏
页码:230 / 238
页数:9
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