The Role of T Cell Immunoglobulin Mucin Domains 1 and 4 in a Herpes Simplex Virus-Induced Behçet’s Disease Mouse Model

Author:

Shim Ju A.1,Lee Eun-So2ORCID,Choi Bunsoon1ORCID,Sohn Seonghyang13ORCID

Affiliation:

1. Laboratory of Cell Biology, Ajou University Institute for Medical Sciences, Suwon 443-721, Republic of Korea

2. Department of Dermatology, Ajou University, School of Medicine, Suwon 443-721, Republic of Korea

3. Brain Korea 21 Project for Medical Science, Suwon 443-721, Republic of Korea

Abstract

The T cell immunoglobulin mucin (TIM) proteins regulate T cell activation and tolerance. TIM-1 plays an important role in the regulation of immune responses and the development of autoimmune diseases. TIM-4 is a natural ligand of TIM-1, and the interaction of TIM-1 and TIM-4 is involved in the regulation of T helper (Th) cell responses and modulation of the Th1/Th2 cytokine balance. Behçet’s disease (BD) is a chronic, multisystemic inflammatory disorder with arthritic, intestinal, mucocutaneous, ocular, vascular, and central nervous system involvement. Tim-1 expression was lower in a herpes simplex virus-induced BD mouse model compared to that in asymptomatic BD normal (BDN) mice. Tim-4 expression was higher in BD mice than that in BDN mice. In this study, we investigated the Tim expression in a BD mouse model with BD-like symptoms. Tim-1 and Tim-4 expression was regulated by an expression vector or siRNA injected into the BD mouse model. TheTim-1vector injected into BD mice resulted in changes in BD-like symptoms and decreased the severity score. Treatment with Tim-4 siRNA also improved BD-like symptoms and decreased the severity score accompanied by upregulation of regulatory T cells. We showed that regulating Tim-1 or Tim-4 affected BD-like symptoms in mice.

Funder

Korea Science and Engineering Foundation

Publisher

Hindawi Limited

Subject

Cell Biology,Immunology

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