B细胞与肠道菌群在时间、空间和地点上的关系

IF 7.4 2区 医学 Q1 IMMUNOLOGY Seminars in Immunology Pub Date : 2023-09-01 DOI:10.1016/j.smim.2023.101806
Oliver Pabst , Carla R. Nowosad
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引用次数: 0

摘要

肠道免疫系统是由与微生物群的持续相互作用形成的。在这里,我们剖析了肠道B细胞反应的时间、空间和上下文层。微生物群影响免疫前B细胞的发育库的选择,该库是B细胞活化、扩增和分化的底物。然而,肠道B细胞反应的各个方面显示出独特的特征。特别是,体细胞突变的B细胞、T细胞缺乏环境中的慢性肠道生发中心以及肠道IgA与微生物群的多反应性结合的出现,对肠道生发中枢的性质和微生物群特异性提出了质疑。我们提出了一个模型来调和这些观察结果,结合了最近证明肠道生发中心微生物群特异性的工作。我们推测,微生物群的佐剂作用可能会改变B细胞进出肠道生发中心的能力。我们提出,时间、空间和地点的分离有助于偶尔令人困惑的肠道B细胞对微生物群反应的讨论。
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B cells and the intestinal microbiome in time, space and place

The gut immune system is shaped by the continuous interaction with the microbiota. Here we dissect temporal, spatial and contextual layers of gut B cell responses. The microbiota impacts on the selection of the developing pool of pre-immune B cells that serves as substrate for B cell activation, expansion and differentiation. However, various aspects of the gut B cell response display unique features. In particular, occurrence of somatically mutated B cells, chronic gut germinal centers in T cell-deficient settings and polyreactive binding of gut IgA to the microbiota questioned the nature and microbiota-specificity of gut germinal centers. We propose a model to reconcile these observations incorporating recent work demonstrating microbiota-specificity of gut germinal centers. We speculate that adjuvant effects of the microbiota might modify permissiveness for B cell to enter and exit gut germinal centers. We propose that separating aspects of time, space and place facilitate the occasionally puzzling discussion of gut B cell responses to the microbiota.

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来源期刊
Seminars in Immunology
Seminars in Immunology 医学-免疫学
CiteScore
11.40
自引率
1.30%
发文量
50
审稿时长
89 days
期刊介绍: Seminars in Immunology is a specialized review journal that serves as a valuable resource for scientists in the field of immunology. The journal's approach is thematic, with each issue dedicated to a specific topic of significant interest to immunologists. It covers a wide range of research areas, from the molecular and cellular foundations of the immune response to the potential for its manipulation, highlighting recent advancements in these areas. Each thematic issue is curated by a guest editor, who is recognized as an expert in the field internationally. The content of each issue typically includes six to eight authoritative invited reviews, which delve into various aspects of the chosen topic. The goal of these reviews is to provide a comprehensive, coherent, and engaging overview of the subject matter, ensuring that the information is presented in a timely manner to maintain its relevance. The journal's commitment to quality and timeliness is further supported by its inclusion in the Scopus database, which is a leading abstract and citation database of peer-reviewed literature. Being indexed in Scopus helps to ensure that the journal's content is accessible to a broad audience of researchers and professionals in immunology and related fields.
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