Dodd Claire E, Schlesinger Larry S
aDepartment of Microbiology bDepartment of Microbial Infection and Immunity, Center for Microbial Interface Biology, The Ohio State University, Columbus, Ohio, USA.
Curr Opin Infect Dis. 2017 Jun;30(3):316-321. doi: 10.1097/QCO.0000000000000367.
Mycobacterium tuberculosis (M.tb), the etiologic agent of tuberculosis, is a prominent global health threat because of the enormous reservoir of subclinical latent tuberculosis infection (LTBI). Current diagnostic approaches are limited in their ability to predict reactivation risk and LTBI is recalcitrant to antibiotic treatment. The present review summarizes recent advances in our ability to detect, treat and model LTBI as well as our understanding of bacterial physiology during latency.
T-cell subsets and circulating proteins have been identified which could serve as biomarkers for LTBI or indicators of reactivation risk. In addition, experimental and in-silico models have enabled discoveries regarding bacterial physiology during latency and the host immune response following infection with latent M.tb.
Despite recent advances, much more research is needed to bolster our ability to detect, implement treatment and model LTBI. The present work is crucial for the eradication of this global problem.
结核分枝杆菌(M.tb)是结核病的病原体,由于存在大量亚临床潜伏性结核感染(LTBI),它对全球健康构成了重大威胁。目前的诊断方法在预测再激活风险方面能力有限,而且LTBI对抗生素治疗具有抗性。本综述总结了我们在检测、治疗和模拟LTBI以及了解潜伏期间细菌生理学方面的最新进展。
已鉴定出可作为LTBI生物标志物或再激活风险指标的T细胞亚群和循环蛋白。此外,实验模型和计算机模拟模型使我们能够发现潜伏期间的细菌生理学以及潜伏性M.tb感染后的宿主免疫反应。
尽管最近取得了进展,但仍需要更多研究来增强我们检测、实施治疗和模拟LTBI的能力。目前的工作对于根除这一全球性问题至关重要。