Oxidization of TGFβ-activated kinase by MPT53 is required for immunity to Mycobacterium tuberculosis

Author:

Wang Lin,Liu Zhonghua,Wang Jie,Liu HaipengORCID,Wu Juehui,Tang Tianqi,Li Haohao,Yang Hua,Qin Lianhua,Ma Dapeng,Chen Jianxia,Liu Feng,Wang Peng,Zheng Ruijuan,Song Peng,Zhou Yilong,Cui Zhenling,Wu Xiangyang,Huang Xiaochen,Liang Haijiao,Zhang Shanshan,Cao Jingjing,Wu Chunyan,Chen Yiping,Su Dan,Chen Xinchun,Zeng Gucheng,Ge BaoxueORCID

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Microbiology (medical),Genetics,Applied Microbiology and Biotechnology,Immunology,Microbiology

Reference56 articles.

1. Kaufmann, S. H. E. et al. Progress in tuberculosis vaccine development and host-directed therapies—a state of the art review. Lancet Respir. Med. 2, 301–320 (2014).

2. World Health Organization. WHO Global Tuberculosis Report 2018 (WHO, 2018).

3. Ottenhoff, T. H. & Kaufmann, S. H. E. Vaccines against tuberculosis: where are we and where do we need to go? PLoS Pathog. 8, e1002607 (2012).

4. Khan, N., Vidyarthi, A., Javed, S. & Agrewala, J. N. Innate immunity holding the flanks until reinforced by adaptive immunity against Mycobacterium tuberculosis infection. Front. Microbiol. 7, 328 (2016).

5. Mayer-Barber, K. D. & Sher, A. Cytokine and lipid mediator networks in tuberculosis. Immunol. Rev. 264, 264–275 (2015).

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