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传染性(非)耐受——受挫的共生关系出了差错?

Infectious (Non)tolerance--frustrated commensalism gone awry?

机构信息

Department of Medicine, University of California, San Francisco, 94143, USA.

出版信息

Cold Spring Harb Perspect Biol. 2012 May 1;4(5):a007328. doi: 10.1101/cshperspect.a007328.

Abstract

Despite advances in medicine, infectious diseases remain major causes of death and disability worldwide. Acute or chronic infectious agents mediate host tissue damage and cause a spectrum of disease as diverse as overwhelming sepsis and shock within hours to persistent tissue inflammation causing organ failure or even cancer over years. Although pathogen exposure can cause disease via host-derived inflammation, pathogens share recognized elements with harmless human commensals. Mouse models and organisms with simpler flora are revealing the dialogue between multicellular hosts and commensal flora. In some instances the persistent inflammation associated with pathogens can be interpreted within a framework of frustrated commensalism in which the host and pathogen cannot complete the requisite dialogue that establishes homeostasis. In contrast, coevolved commensals interact cooperatively with the host immune system, resulting in immunotolerance. Attempts to more thoroughly understand the molecular nature of the dialogue may uncover novel approaches to the control of inflammation and tissue damage.

摘要

尽管医学取得了进步,但传染病仍然是全球范围内死亡和残疾的主要原因。急性或慢性传染病可介导宿主组织损伤,并导致一系列疾病,从数小时内导致压倒性的败血症和休克到持续的组织炎症导致器官衰竭甚至数年的癌症不等。尽管病原体暴露可以通过宿主来源的炎症引起疾病,但病原体与无害的人类共生菌有共同的特征。小鼠模型和具有更简单菌群的生物体正在揭示多细胞宿主与共生菌群之间的对话。在某些情况下,与病原体相关的持续炎症可以用受挫共生的框架来解释,在这种框架下,宿主和病原体无法完成建立体内平衡所必需的对话。相比之下,共同进化的共生菌与宿主免疫系统合作,导致免疫耐受。试图更彻底地了解对话的分子本质可能会揭示控制炎症和组织损伤的新方法。

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