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肺外对呼吸防御的控制。

Extra-pulmonary control of respiratory defense.

机构信息

Department of Medicine, Division of Immunology and Infectious Disease, UMass Chan Medical School, Worcester, MA 01602, United States.

Department of Medicine, Division of Immunology and Infectious Disease, UMass Chan Medical School, Worcester, MA 01602, United States.

出版信息

Cell Immunol. 2024 Jul-Aug;401-402:104841. doi: 10.1016/j.cellimm.2024.104841. Epub 2024 Jun 7.

DOI:10.1016/j.cellimm.2024.104841
PMID:38878619
Abstract

Pneumonia persists as a public health crisis, representing the leading cause of death due to infection. Whether respiratory tract infections progress to pneumonia and its sequelae such as acute respiratory distress syndrome and sepsis depends on numerous underlying conditions related to both the causative agent and host. Regarding the former, pneumonia burden remains staggeringly high, despite the effectiveness of pathogen-targeting strategies such as vaccines and antibiotics. This demands a greater understanding of host features that collaborate to promote immune resistance and tissue resilience in the infected lung. Such features inside the pulmonary compartment have drawn much attention, where major advances have been made related to resident and recruited immune activity. By comparison, extra-pulmonary processes guiding pneumonia susceptibility are relatively elusive, constituting the focus of this review. Here we will highlight examples of when, how, and why tissues outside of the lungs dispatch signals that modulate local immunity in the airspaces. Topics include the liver, gut, bone marrow, brain and more, all of which contribute in direct and indirect ways to pneumonia outcome. When tuned appropriately, it has become clear that these responses can serve protective roles, and this will be considered distinctly from what would otherwise be aberrant responses characteristic of pneumonia-induced organ injury and sepsis. Further advances in this area may reveal novel targetable areas for clinical intervention that are not confined to the intra-pulmonary space.

摘要

肺炎仍然是一个公共卫生危机,是感染导致死亡的主要原因。呼吸道感染是否会发展为肺炎及其后遗症,如急性呼吸窘迫综合征和败血症,取决于与病原体和宿主都相关的许多潜在条件。尽管针对病原体的策略(如疫苗和抗生素)非常有效,但肺炎的负担仍然高得惊人。这就需要更多地了解宿主的特征,这些特征有助于促进感染肺部的免疫抵抗和组织弹性。肺部内的这些特征引起了广泛关注,在这些特征方面已经取得了重大进展,涉及驻留和募集的免疫活性。相比之下,指导肺炎易感性的肺外过程相对难以捉摸,这构成了本综述的重点。在这里,我们将重点介绍肺部以外的组织发出信号调节肺部局部免疫的时间、方式和原因的例子。这些话题包括肝脏、肠道、骨髓、大脑等,所有这些都以直接和间接的方式影响肺炎的结果。当这些反应被适当调节时,很明显,这些反应可以起到保护作用,这将与肺炎引起的器官损伤和败血症的异常反应明显区分开来。在这一领域的进一步进展可能会揭示新的可靶向的临床干预领域,而不仅仅局限于肺内空间。

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本文引用的文献

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Prevention of respiratory virus transmission by resident memory CD8 T cells.通过驻留记忆 CD8 T 细胞预防呼吸道病毒传播。
Nature. 2024 Feb;626(7998):392-400. doi: 10.1038/s41586-023-06937-1. Epub 2023 Dec 12.
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Neurological disorders after severe pneumonia are associated with translocation of endogenous bacteria from the lung to the brain.严重肺炎后的神经紊乱与内源性细菌从肺部转移到大脑有关。
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Butyrate protects against MRSA pneumonia via regulating gut-lung microbiota and alveolar macrophage M2 polarization.
丁酸盐通过调节肠道-肺部微生物群和肺泡巨噬细胞 M2 极化来预防耐甲氧西林金黄色葡萄球菌肺炎。
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Genetically determined thymic function affects strength and duration of immune response in COVID patients with pneumonia.遗传决定的胸腺功能影响肺炎 COVID 患者免疫反应的强度和持续时间。
Sci Adv. 2023 Sep 22;9(38):eadh7969. doi: 10.1126/sciadv.adh7969.
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Maternal diet modulates the infant microbiome and intestinal Flt3L necessary for dendritic cell development and immunity to respiratory infection.母体饮食可调节婴儿微生物群和肠道 Flt3L,这对于树突状细胞发育和呼吸道感染免疫至关重要。
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Re-defining the Gut Heart Axis: A Systematic Review of the Literature on the Role of Gut Microbial Dysbiosis in Patients With Heart Failure.重新定义肠道-心脏轴:关于肠道微生物群失调在心力衰竭患者中作用的文献系统综述
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9
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Lung epithelial cell-derived C3 protects against pneumonia-induced lung injury.肺上皮细胞衍生的 C3 可预防肺炎引起的肺损伤。
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