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Regulatory T Cells in Type 1 Autoimmune Pancreatitis
Author(s) -
Kazushige Uchida,
Takeo Kusuda,
Masanori Koyabu,
Hideaki Miyoshi,
Norimasa Fukata,
Kimi Sumimoto,
Yuri Fukui,
Yutaku Sakaguchi,
Tsukasa Ikeura,
Masaaki Shimatani,
Toshiro Fukui,
Mitsunobu Matsushita,
Makoto Takaoka,
Akiyoshi Nishio,
Kazuichi Okazaki
Publication year - 2012
Publication title -
international journal of rheumatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.8
H-Index - 33
eISSN - 1687-9279
pISSN - 1687-9260
DOI - 10.1155/2012/795026
Subject(s) - autoimmune pancreatitis , medicine , pancreatitis , computational biology , immunology , biology
Autoimmune pancreatitis (AIP) is a newly recognized pancreatic disorder. Recently, International Consensus Diagnostic Criteria for AIP (ICDC) was published. In this ICDC, AIP was classified into Type 1 and Type 2. Patients with Type 1 AIP have several immunologic and histologic abnormalities specific to the disease, including increased levels of serum IgG4 and storiform fibrosis with infiltration of lymphocytes and IgG4-positive plasmacytes in the involved organs. Among the involved organs showing extrapancreatic lesions, the bile duct is the most common, exhibiting sclerosing cholangitis (IgG4-SC). However, the role of IgG4 is unclear. Recently, it has been reported that regulatory T cells (Tregs) are involved in both the development of various autoimmune diseases and the shift of B cells toward IgG4, producing plasmacytes. Our study showed that Tregs were increased in the pancreas with Type 1 AIP and IgG4-SC compared with control. In the patients with Type 1 AIP and IgG4-SC, the numbers of infiltrated Tregs were significantly positively correlated with IgG4-positive plasma cells. In Type 1 AIP, inducible costimulatory molecule (ICOS) + and IL-10 + Tregs significantly increased compared with control groups. Our data suggest that increased quantities of ICOS + Tregs may influence IgG4 production via IL-10 in Type 1 AIP.

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