结核性肉芽肿与既往免疫。

IF 26.9 1区 医学 Q1 IMMUNOLOGY Annual review of immunology Pub Date : 2022-04-26 Epub Date: 2022-02-07 DOI:10.1146/annurev-immunol-093019-125148
Sara B Cohen, Benjamin H Gern, Kevin B Urdahl
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引用次数: 16

摘要

肺肉芽肿被广泛认为是对结核分枝杆菌(Mtb)免疫反应的中心,结核分枝杆菌是结核病的病原体。最近的动物研究揭示了促进或限制肉芽肿内结核病免疫的因素。然而,这些模型通常忽略了先前存在的免疫对细胞组织和功能的影响,这是一个重要的考虑因素,因为大多数结核病可能是通过先前暴露的个体的再感染发生的。前抗生素时代的人类死后研究表明,Mtb-naïve个体(原发结核)感染与先前接触结核分枝杆菌(原发结核后)的感染具有明显的病理特征。我们回顾了最近在结核病肉芽肿生物学中的动物发现,这些发现在很大程度上反映了原发性结核病。我们还讨论了我们目前对原发后结核病病变的理解,关于这一点我们知之甚少。许多知识空白仍然存在,特别是关于先前存在的免疫如何影响肉芽肿结构和结核分枝杆菌感染部位的局部免疫反应。
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The Tuberculous Granuloma and Preexisting Immunity.

Pulmonary granulomas are widely considered the epicenters of the immune response to Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis (TB). Recent animal studies have revealed factors that either promote or restrict TB immunity within granulomas. These models, however, typically ignore the impact of preexisting immunity on cellular organization and function, an important consideration because most TB probably occurs through reinfection of previously exposed individuals. Human postmortem research from the pre-antibiotic era showed that infections in Mtb-naïve individuals (primary TB) versus those with prior Mtb exposure (postprimary TB) have distinct pathologic features. We review recent animal findings in TB granuloma biology, which largely reflect primary TB. We also discuss our current understanding of postprimary TB lesions, about which much less is known. Many knowledge gaps remain, particularly regarding how preexisting immunity shapes granuloma structure and local immune responses at Mtb infection sites.

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来源期刊
Annual review of immunology
Annual review of immunology 医学-免疫学
CiteScore
57.20
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Immunology, in publication since 1983, focuses on basic immune mechanisms and molecular basis of immune diseases in humans. Topics include innate and adaptive immunity; immune cell development and differentiation; immune control of pathogens (viruses, bacteria, parasites) and cancer; and human immunodeficiency and autoimmune diseases. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license.
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