Messenger RNA expression of IL-8, FOXP3, and IL-12β differentiates latent tuberculosis infection from disease

被引:58
作者
Wu, Bo
Huang, Chunhong
Kato-Maeda, Midori
Hopewell, Philip C.
Daley, Charles L.
Krensky, Alan M.
Clayberger, Carol
机构
[1] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Div Pulm & Crit Care Med, San Francisco, CA 94110 USA
[3] Natl Jewish Med & Res Ctr, Div Mycobacterial & Resp Infect, Denver, CO 80206 USA
关键词
D O I
10.4049/jimmunol.178.6.3688
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Differentiation of active from latent tuberculosis (TB) is a major. challenge in the control of TB. In this study, PBMC from latent TB-infected subjects, TB patients, and tuberculin skin test-negative donors stimulated with the Mycobacterium tuberculosis (Mtb)-specific Ag, early secretory antigenic target 6, and mRNA for 45 immune-related genes was measured by quantitative real-time PCR. Univariate analysis showed significant differences in the expression of 10 genes (IFN-gamma, FOXP3, IL-1 alpha, IL-1 beta, IL-2, IL-6, IL-8, IL-12 alpha, IL-12 beta, and IL-24) in PBMC from TB patients vs latent TB-infected subjects (p < 0.01). Multivariate logistic regression and classification and regression tree analyses revealed that expression of three genes, IL-8, FOXP3, and IL-12 beta, is predictive for TB vs latent Mtb infection. Thus, measurement of Ag-specific expression of these three genes may offer a specific and noninvasive means of differentiating between latent Mtb infection and TB.
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收藏
页码:3688 / 3694
页数:7
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