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重新审视结核病的自然史。纳入持续再感染、宿主耐受和损伤反应框架,有助于更好地理解潜伏感染及其向活动性疾病的演变。

Revisiting the natural history of tuberculosis. The inclusion of constant reinfection, host tolerance, and damage-response frameworks leads to a better understanding of latent infection and its evolution towards active disease.

机构信息

Unitat de Tuberculosi Experimental, Department of Microbiology, Fundació Institut per a la Investigació en Ciències de la Salut Germans Trias i Pujol, Universitat Autònoma de Barcelona, Crta. del can Ruti, camí de les escoles s/n, Badalona, Catalonia, Spain.

出版信息

Arch Immunol Ther Exp (Warsz). 2010 Feb;58(1):7-14. doi: 10.1007/s00005-009-0062-5. Epub 2010 Jan 5.

Abstract

Once Mycobacterium tuberculosis infects a person it can persist for a long time in a process called latent tuberculosis infection (LTBI). LTBI has traditionally been considered to involve the bacilli remaining in a non-replicating state (dormant) in old lesions but still retaining their ability to induce reactivation and cause active tuberculosis (TB) once a disruption of the immune response takes place. The present review aims to challenge these concepts by including recent experimental data supporting LTBI as a constant endogenous reinfection process as well as the recently introduced concepts of damage-response and tolerance frameworks to explain TB induction. These frameworks highlight the key role of an exaggerated and intolerant host response against M. tuberculosis bacilli which induces the classical TB cavity in immunocompetent adults once the constant endogenous reinfection process has resulted in the presence of bacilli in the upper lobes, where they can grow faster and the immune response is delayed. This essay intends to provide new clues to understanding the induction of TB in non-immunosuppressed patients.

摘要

一旦结核分枝杆菌感染人体,它就可以在潜伏期结核感染(LTBI)过程中长时间存在。LTBI 传统上被认为涉及细菌以非复制状态(休眠)留在旧病灶中,但仍保留其在免疫反应发生破坏时引起活动性结核病(TB)的能力。本综述旨在通过包括最近支持 LTBI 作为持续内源性再感染过程的实验数据以及最近提出的损伤-反应和耐受框架概念来挑战这些概念,以解释 TB 的诱导。这些框架强调了宿主对结核分枝杆菌的过度和不耐受反应的关键作用,一旦持续的内源性再感染过程导致上叶存在细菌,这种反应就会导致经典的 TB 空洞,在那里它们可以更快地生长,免疫反应会延迟。本文旨在为理解非免疫抑制患者 TB 的诱导提供新的线索。

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