Stromal cells in tertiary lymphoid structures: Architects of autoimmunity

被引:31
作者
Asam, Saba [1 ]
Nayar, Saba [1 ,2 ]
Gardner, David [1 ]
Barone, Francesca [1 ]
机构
[1] Univ Birmingham, Inst Inflammat & Ageing, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Univ Hosp Birmingham NHS Fdn Trust, BNIHR Birmingham Biomed Res Ctr, Birmingham, W Midlands, England
关键词
tertiary lymphoid organs; fibroblasts; stromal cells; inflammatory cytokines; autoimmunity; FIBROBLASTIC RETICULAR CELLS; DENDRITIC CELLS; B-CELLS; SJOGREN SYNDROME; IMMUNE CELLS; T-CELLS; LYMPHOTOXIN; CANCER; INFLAMMATION; EXPRESSION;
D O I
10.1111/imr.12987
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The molecular mediators present within the inflammatory microenvironment are able, in certain conditions, to favor the initiation of tertiary lymphoid structure (TLS) development. TLS is organized lymphocyte clusters able to support antigen-specific immune response in non-immune organs. Importantly, chronic inflammation does not always result in TLS formation; instead, TLS has been observed to develop specifically in permissive organs, suggesting the presence of tissue-specific cues that are able to imprint the immune responses and form TLS hubs. Fibroblasts are tissue-resident cells that define the anatomy and function of a specific tissue. Fibroblast plasticity and specialization in inflammatory conditions have recently been unraveled in both immune and non-immune organs revealing a critical role for these structural cells in human physiology. Here, we describe the role of fibroblasts in the context of TLS formation and its functional maintenance in the tissue, highlighting their potential role as therapeutic disease targets in TLS-associated diseases.
引用
收藏
页码:184 / 195
页数:12
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