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Chinese Journal of Antituberculosis ›› 2026, Vol. 48 ›› Issue (8): 1214-1219.doi: 10.19982/j.issn.1000-6621.20260098

• Review Articles • Previous Articles     Next Articles

Advances in Mycobacterium tuberculosis regulation of host lipid metabolism reprogramming

Zeng Lina1,2, Li Wensi2,3, Lu Hailin2,3, Wang Wenfei2, Chen Xinchun3, Deng Guofang4(), Xie Shuixiang1()   

  1. 1 School of Basic Medicine, Gannan Medical University, Ganzhou 341000, China
    2 National Clinical Research Center for Infectious Diseases, Shenzhen 518000, China
    3 Shenzhen University School of Medicine, Shenzhen 518000, China
    4 Division Two of Pulmonary Diseases, The Third People’s Hospital of Shenzhen, Shenzhen 518000, China
  • Received:2026-02-25 Online:2026-08-01 Published:2026-07-30
  • Contact: Deng Guofang, Email: jxxk1035@yeah.net; Xie Shuixiang, Email: xsxw2002@163.com
  • Supported by:
    Research Fund of The Third People’s Hospital of Shenzhen(G202205);Research Fund of The Third People’s Hospital of Shenzhen(G2022003);Research Fund of The Third People’s Hospital of Shenzhen(G2022155);Research Fund of The Third People’s Hospital of Shenzhen(24250G1025)

Abstract:

Tuberculosis is a major global infectious disease caused by Mycobacterium tuberculosis (MTB). The pathogen’s ability to establish long-term persistence and evade host immunity is central to the development of chronic infection. Lipid metabolism plays a pivotal role in host-pathogen interactions: MTB not only actively hijacks host lipids as a nutrient source but also systematically reprograms the host lipid metabolic network to evade immune clearance and establish persistent infection. A deeper understanding of the molecular mechanisms by which MTB hijacks and reprograms host lipid metabolism provides important theoretical foundations and potential targets for the development of host-directed therapies focusing on host lipid metabolism. This review systematically summarizes the molecular mechanisms by which MTB hijacks host lipids as a nutrient source and reprograms host lipid metabolism to achieve immune evasion, and discusses future research directions and clinical translation prospects in this field.

Key words: Mycobacterium tuberculosis, Macrophages, Lipid metabolism, Host-pathogen interactions

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