Feldman Charles, Theron Annette J, Cholo Moloko C, Anderson Ronald
Department of Internal Medicine, Faculty of Health Sciences, University of the Witwatersrand, York Road, Parktown, Johannesburg 2193, South Africa.
Department of Immunology, School of Medicine, Faculty of Health Sciences, University of Pretoria, Bophelo Road, Prinshof, Pretoria 0083, South Africa.
Pathogens. 2024 Feb 7;13(2):151. doi: 10.3390/pathogens13020151.
It has been noted by the World Health Organisation that cases of tuberculosis in 2022 globally numbered 10.6 million, resulting in 1.3 million deaths, such that TB is one of the infectious diseases causing the greatest morbidity and mortality worldwide. Since as early as 1918, there has been an ongoing debate as to the relationship between cigarette smoking and TB. However, numerous epidemiological studies, as well as meta-analyses, have indicated that both active and passive smoking are independent risk factors for TB infection, development of reactivation TB, progression of primary TB, increased severity of cavitary disease, and death from TB, among several other considerations. With this considerable body of evidence confirming the association between smoking and TB, it is not surprising that TB control programmes represent a key potential preventative intervention. In addition to coverage of the epidemiology of TB and its compelling causative link with smoking, the current review is also focused on evidence derived from clinical- and laboratory-based studies of disease pathogenesis, most prominently the protective anti-mycobacterial mechanisms of the alveolar macrophage, the primary intracellular refuge of . This section of the review is followed by an overview of the major strategies utilised by the pathogen to subvert these antimicrobial mechanisms in the airway, which are intensified by the suppressive effects of smoke inhalation on alveolar macrophage function. Finally, consideration is given to a somewhat under-explored, pro-infective activity of cigarette smoking, namely augmentation of antibiotic resistance due to direct effects of smoke per se on the pathogen. These include biofilm formation, induction of cellular efflux pumps, which eliminate both smoke-derived toxicants and antibiotics, as well as gene modifications that underpin antibiotic resistance.
世界卫生组织指出,2022年全球结核病病例达1060万,导致130万人死亡,因此结核病是全球发病率和死亡率最高的传染病之一。早在1918年,关于吸烟与结核病之间的关系就一直存在争论。然而,众多流行病学研究以及荟萃分析表明,主动吸烟和被动吸烟都是结核病感染、复发性结核病发展、原发性结核病进展、空洞性疾病严重程度增加以及结核病死亡等多种情况的独立危险因素。有了大量证据证实吸烟与结核病之间的关联,结核病控制项目成为关键的潜在预防干预措施也就不足为奇了。除了涵盖结核病流行病学及其与吸烟的令人信服的因果关系外,本综述还聚焦于基于临床和实验室的疾病发病机制研究得出的证据,最突出的是肺泡巨噬细胞的保护性抗分枝杆菌机制,肺泡巨噬细胞是结核分枝杆菌的主要细胞内庇护所。本综述的这一部分之后是对病原体在气道中颠覆这些抗菌机制所采用的主要策略的概述,吸入烟雾对肺泡巨噬细胞功能的抑制作用会强化这些策略。最后,考虑了吸烟一种尚未充分探索的促感染活性,即烟雾本身对病原体的直接作用导致抗生素耐药性增加。这些包括生物膜形成、诱导细胞外排泵(其可清除烟雾衍生的毒物和抗生素)以及支撑抗生素耐药性的基因修饰。