Shah Javeed A, Musvosvi Munyaradzi, Shey Muki, Horne David J, Wells Richard D, Peterson Glenna J, Cox Jeffery S, Daya Michelle, Hoal Eileen G, Lin Lin, Gottardo Raphael, Hanekom Willem A, Scriba Thomas J, Hatherill Mark, Hawn Thomas R
1 University of Washington School of Medicine, Seattle, Washington.
2 Veterans Affairs Puget Sound Health Care System, Seattle, Washington.
Am J Respir Crit Care Med. 2017 Aug 15;196(4):502-511. doi: 10.1164/rccm.201611-2346OC.
The molecular mechanisms that regulate tuberculosis susceptibility and bacillus Calmette-Guérin (BCG)-induced immunity are mostly unknown. However, induction of the adaptive immune response is a critical step in host control of Mycobacterium tuberculosis. Toll-interacting protein (TOLLIP) is a ubiquitin-binding protein that regulates innate immune responses, including Toll-like receptor signaling, which initiate adaptive immunity. TOLLIP variation is associated with susceptibility to tuberculosis, but the mechanism by which it regulates tuberculosis immunity is poorly understood.
To identify functional TOLLIP variants and evaluate the role of TOLLIP variation on innate and adaptive immune responses to mycobacteria and susceptibility to tuberculosis.
We used human cellular immunology approaches to characterize the role of a functional TOLLIP variant on monocyte mRNA expression and M. tuberculosis-induced monocyte immune functions. We also examined the association of TOLLIP variation with BCG-induced T-cell responses and susceptibility to latent tuberculosis infection.
We identified a functional TOLLIP promoter region single-nucleotide polymorphism, rs5743854, which was associated with decreased TOLLIP mRNA expression in infant monocytes. After M. tuberculosis infection, TOLLIP-deficient monocytes demonstrated increased IL-6, increased nitrite, and decreased bacterial replication. The TOLLIP-deficiency G/G genotype was associated with decreased BCG-specific IL-2 CD4 T-cell frequency and proliferation. This genotype was also associated with increased susceptibility to latent tuberculosis infection.
TOLLIP deficiency is associated with decreased BCG-specific T-cell responses and increased susceptibility to tuberculosis. We hypothesize that the heightened antibacterial monocyte responses after vaccination of TOLLIP-deficient infants are responsible for decreased BCG-specific T-cell responses. Activating TOLLIP may provide a novel adjuvant strategy for BCG vaccination.
调节结核病易感性和卡介苗(BCG)诱导免疫的分子机制大多未知。然而,适应性免疫反应的诱导是宿主控制结核分枝杆菌的关键步骤。Toll相互作用蛋白(TOLLIP)是一种泛素结合蛋白,可调节包括Toll样受体信号传导在内的先天免疫反应,而Toll样受体信号传导可启动适应性免疫。TOLLIP变异与结核病易感性相关,但其调节结核病免疫的机制尚不清楚。
鉴定功能性TOLLIP变异体,并评估TOLLIP变异对分枝杆菌先天和适应性免疫反应以及结核病易感性的作用。
我们采用人类细胞免疫学方法来表征功能性TOLLIP变异体对单核细胞mRNA表达和结核分枝杆菌诱导的单核细胞免疫功能的作用。我们还研究了TOLLIP变异与卡介苗诱导的T细胞反应以及潜伏性结核感染易感性之间的关联。
我们鉴定出一个功能性TOLLIP启动子区域单核苷酸多态性rs5743854,它与婴儿单核细胞中TOLLIP mRNA表达降低相关。结核分枝杆菌感染后,缺乏TOLLIP的单核细胞表现出IL-6增加、亚硝酸盐增加和细菌复制减少。缺乏TOLLIP的G/G基因型与卡介苗特异性IL-2 CD4 T细胞频率和增殖降低相关。该基因型还与潜伏性结核感染易感性增加相关。
TOLLIP缺乏与卡介苗特异性T细胞反应降低和结核病易感性增加相关。我们推测,TOLLIP缺乏的婴儿接种疫苗后单核细胞抗菌反应增强是卡介苗特异性T细胞反应降低的原因。激活TOLLIP可能为卡介苗接种提供一种新的佐剂策略。