Xiong Kunlong, Sun Wenwen, He Yayi, Fan Lin
Shanghai Clinical Research Center for Infectious Disease (Tuberculosis), Department of Tuberculosis, Shanghai Key Laboratory of Tuberculosis, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Department of Tuberculosis, Tongji University, Shanghai, China.
Transl Lung Cancer Res. 2021 Oct;10(10):4012-4026. doi: 10.21037/tlcr-21-465.
We systematically review the molecular mechanism of the interaction between lung cancer (LC) and tuberculosis (TB), and put forward the existing problems in order to provide suggestions for early intervention and future research direction.
TB and LC are two global public health problems affecting human health. LC is the main cause of cancer-related death worldwide and TB is one of the leading causes of death among infectious diseases, especially in resource-poor areas. Previous studies have suggested that a history of TB may be associated with an increased risk of LC. With the improvement of LC treatment, the occurrence of pulmonary tuberculosis in the course of LC treatment is also frequently reported recently.
The molecular immunological mechanisms of interaction between LC and TB, and related epidemiological literature are reviewed. The research progress and problems to be solved are summarized.
Chronic inflammation, immune abnormalities, scar formation, gene mutations and drug effects caused by TB may be associated with the occurrence of LC induced by abnormalities in various molecular pathways. LC and decreased immunity during treatment may also increase the risk of latent TB activation or new TB infection through immune pathways. Data on dual burden areas of TB and LC are still lacking, and more clinical studies are needed to elucidate the association.
系统综述肺癌(LC)与结核病(TB)相互作用的分子机制,并提出存在的问题,为早期干预及未来研究方向提供建议。
结核病和肺癌是影响人类健康的两个全球性公共卫生问题。肺癌是全球癌症相关死亡的主要原因,结核病是传染病死亡的主要原因之一,尤其是在资源匮乏地区。既往研究提示,结核病病史可能与肺癌风险增加有关。随着肺癌治疗的改善,近期在肺癌治疗过程中发生肺结核的报道也屡见不鲜。
综述肺癌与结核病相互作用的分子免疫学机制及相关流行病学文献。总结研究进展及有待解决的问题。
结核病引起的慢性炎症、免疫异常、瘢痕形成、基因突变及药物作用可能与各种分子途径异常诱导的肺癌发生有关。肺癌及治疗期间免疫力下降也可能通过免疫途径增加潜伏性结核激活或新发结核感染的风险。结核病和肺癌双重负担地区的数据仍然缺乏,需要更多的临床研究来阐明两者之间的关联。