| Literature DB >> 34403362 |
Hui Wang1, Xiaofei Li1, Tetsuhiro Kajikawa1, Jieun Shin1, Jong-Hyung Lim1, Ioannis Kourtzelis2,3, Kosuke Nagai2, Jonathan M Korostoff4, Sylvia Grossklaus2, Ronald Naumann5, Triantafyllos Chavakis2,6, George Hajishengallis1.
Abstract
The secreted protein developmental endothelial locus 1 (DEL-1) regulates inflammatory cell recruitment and protects against inflammatory pathologies in animal models. Here, we investigated DEL-1 in inflammatory arthritis using collagen-induced arthritis (CIA) and collagen Ab-induced arthritis (CAIA) models. In both models, mice with endothelium-specific overexpression of DEL-1 were protected from arthritis relative to WT controls, whereas arthritis was exacerbated in DEL-1-deficient mice. Compared with WT controls, mice with collagen VI promoter-driven overexpression of DEL-1 in mesenchymal cells were protected against CIA but not CAIA, suggesting a role for DEL-1 in the induction of the arthritogenic Ab response. Indeed, DEL-1 was expressed in perivascular stromal cells of the lymph nodes and inhibited Tfh and germinal center B cell responses. Mechanistically, DEL-1 inhibited DC-dependent induction of Tfh cells by targeting the LFA-1 integrin on T cells. Overall, DEL-1 restrained arthritis through a dual mechanism, one acting locally in the joints and associated with the anti-recruitment function of endothelial cell-derived DEL-1; the other mechanism acting systemically in the lymph nodes and associated with the ability of stromal cell-derived DEL-1 to restrain Tfh responses. DEL-1 may therefore be a promising therapeutic for the treatment of inflammatory arthritis.Entities:
Keywords: Adaptive immunity; Antigen-presenting cells; Autoimmunity; Inflammation; T cells
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Year: 2021 PMID: 34403362 PMCID: PMC8483759 DOI: 10.1172/JCI150578
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808