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中国防痨杂志 ›› 2026, Vol. 48 ›› Issue (3): 419-425.doi: 10.19982/j.issn.1000-6621.20250397

• 综述 • 上一篇    下一篇

脓肿分枝杆菌复合群感染导致肺损伤的机制研究进展

倪盛1, 沙巍2, 王丽2()   

  1. 1同济大学医学院,上海 200092
    2同济大学附属上海市肺科医院结核科,上海 200433
  • 收稿日期:2025-10-09 出版日期:2026-03-10 发布日期:2026-03-06
  • 通信作者: 王丽 E-mail:wangli_shph@tongji.edu.cn
  • 基金资助:
    科技部重点研发计划“病原学专项”子课题(2023YFC2307303);中央高校基本科研业务费专项资金资助(同济大学自主原创基础研究22120240329);上海市申康医院发展中心市级医院诊疗推广及优化管理项目(SHDC12022108)

Research progress on the mechanisms of lung injury caused by Mycobacterium abscessus

Ni Sheng1, Sha Wei2, Wang Li2()   

  1. 1Tongji University School of Medicine, Shanghai 200092, China
    2Department of Tuberculosis, Shanghai Pulmonary Hospital, School of Medicine, TongJi University, Shanghai 200433, China
  • Received:2025-10-09 Online:2026-03-10 Published:2026-03-06
  • Contact: Wang Li E-mail:wangli_shph@tongji.edu.cn
  • Supported by:
    National Key R&D Program of China (Pathogen Research)-Sub-project(2023YFC2307303);Fundamental Research Funds for the Central Universities(Tongji University Independent Original Basic Research 22120240329);Shanghai Shenkang Hospital Development Center Municipal Hospital Clinical Research and Management Optimization Program(SHDC12022108)

摘要:

脓肿分枝杆菌复合群(Mycobacterium abscessus complex, MABC)具有高毒力、高耐药性,其导致肺损伤的机制较为复杂,主要由宿主免疫应答失衡及组织修复异常共同驱动。笔者对近年来有关MABC导致肺损伤的机制进行综述,重点聚焦于过度炎症反应及异常修复,以厘清疾病发展的关键节点,为未来针对特定环节的深入研究奠定基础。

关键词: 分枝杆菌,脓肿, 感染, 免疫, 综述

Abstract:

Mycobacterium abscessus complex (MABC) has high virulence and high drug resistance. The mechanisms of lung injury causing by MABC are complicated, mainly caused by the imbalance of host immune response and abnormal tissue repair. This review summarizes current researches on the mechanisms of MABC-induced lung injury, focusing especially on the roles of excessive inflammatory responses and abnormal repair processes, to identify crucial points of the disease development, to set the stage for more focused researches into particular pathogenic stages.

Key words: Mycobacterium abscessus, Infection, Immunity, Review

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