PILRα negatively regulates mouse inflammatory arthritis

Paired Ig-like type 2 receptor (PILR)α inhibitory receptor and its counterpart PILRβ activating receptor are coexpressed on myeloid cells. In this article, we report that PILRα, but not PILRβ, is elevated in human rheumatoid arthritis synovial tissue and correlates with inflammatory cell infiltratio...

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Published in:The Journal of immunology (1950) Vol. 193; no. 2; pp. 860 - 870
Main Authors: Sun, Yonglian, Caplazi, Patrick, Zhang, Juan, Mazloom, Anita, Kummerfeld, Sarah, Quinones, Gabriel, Senger, Kate, Lesch, Justin, Peng, Ivan, Sebrell, Andrew, Luk, Wilman, Lu, Yanmei, Lin, Zhonghua, Barck, Kai, Young, Judy, Del Rio, Mariela, Lehar, Sophie, Asghari, Vida, Lin, WeiYu, Mariathasan, Sanjeev, DeVoss, Jason, Misaghi, Shahram, Balazs, Mercedesz, Sai, Tao, Haley, Benjamin, Hass, Philip E, Xu, Min, Ouyang, Wenjun, Martin, Flavius, Lee, Wyne P, Zarrin, Ali A
Format: Journal Article
Language:English
Published: United States 15-07-2014
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Summary:Paired Ig-like type 2 receptor (PILR)α inhibitory receptor and its counterpart PILRβ activating receptor are coexpressed on myeloid cells. In this article, we report that PILRα, but not PILRβ, is elevated in human rheumatoid arthritis synovial tissue and correlates with inflammatory cell infiltration. Pilrα(-/-) mice produce more pathogenic cytokines during inflammation and are prone to enhanced autoimmune arthritis. Correspondingly, engaging PILRα with anti-PILRα mAb ameliorates inflammation in mouse arthritis models and suppresses the production of proinflammatory cytokines. Our studies suggest that PILRα mediates an important inhibitory pathway that can dampen inflammatory responses.
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ISSN:0022-1767
1550-6606
DOI:10.4049/jimmunol.1400045