Key Laboratory of Regional Characteristic Agricultural Resources, College of Life Sciences, Neijiang Normal University, Neijiang, Sichuan 641100, China.
Key Laboratory of Molecular Biology for Infectious Diseases (Ministry of Education), Institute for Viral Hepatitis, Department of Infectious Diseases, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
J Immunol Res. 2018 Oct 22;2018:1535194. doi: 10.1155/2018/1535194. eCollection 2018.
Tuberculosis, caused by , remains a leading cause of morbidity and mortality globally, with nearly 10.4 million new cases of incidence and over 1.7 million deaths annually. Drug-resistant strains, especially multidrug-resistant or extensively drug-resistant strains, have further intensified the problem associated with tuberculosis control. Host-directed therapy is a promising alternative for tuberculosis control. IL-32 is increasingly recognized as an important host molecule against tuberculosis. In this review, we highlight the proinflammatory properties of IL-32 and the mode of action of IL-32 in mycobacterial infections to inspire the development of novel immunity-based countermeasures and host-directed therapies against tuberculosis.
结核病是由 引起的,仍然是全球发病率和死亡率的主要原因,每年有近 1040 万例新发病例和超过 170 万人死亡。耐药菌株,特别是耐多药或广泛耐药菌株,进一步加剧了与结核病控制相关的问题。宿主导向治疗是结核病控制的一种有前途的替代方法。IL-32 被认为是对抗结核病的重要宿主分子。在这篇综述中,我们强调了 IL-32 的促炎特性和 IL-32 在分枝杆菌感染中的作用模式,以激发针对结核病的新型基于免疫的对策和宿主导向疗法的开发。