| Literature DB >> 29431690 |
Joseph R Podojil1, Iris Hecht2, Ming-Yi Chiang1, Ilan Vaknin2, Inbal Barbiro2, Amit Novik2, Eyal Neria2, Galit Rotman2, Stephen D Miller3.
Abstract
ILDR2 is a member of the Ig superfamily, which is implicated in tricellular tight junctions, and has a putative role in pancreatic islet health and survival. We recently found a novel role for ILDR2 in delivering inhibitory signals to T cells. In this article, we show that short-term treatment with ILDR2-Fc results in long-term durable beneficial effects in the relapsing-remitting experimental autoimmune encephalomyelitis and NOD type 1 diabetes models. ILDR2-Fc also promotes transplant engraftment in a minor mismatch bone marrow transplantation model. ILDR2-Fc displays a unique mode of action, combining immunomodulation, regulation of immune homeostasis, and re-establishment of Ag-specific immune tolerance via regulatory T cell induction. These findings support the potential of ILDR-Fc to provide a promising therapeutic approach for the treatment of autoimmune diseases.Entities:
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Year: 2018 PMID: 29431690 PMCID: PMC6830572 DOI: 10.4049/jimmunol.1700326
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422