Regulatory T Cells in Type 1 Autoimmune Pancreatitis

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 specifi...

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Veröffentlicht in:International Journal of Rheumatology 2012-01, Vol.2012 (2012), p.314-319
Hauptverfasser: Koyabu, Masanori, Kusuda, Takeo, Uchida, Kazushige, Miyoshi, Hideaki, Fukata, Norimasa, Sumimoto, Kimi, Fukui, Yuri, Sakaguchi, Yutaku, Ikeura, Tsukasa, Shimatani, Masaaki, Fukui, Toshiro, Matsushita, Mitsunobu, Takaoka, Makoto, Nishio, Akiyoshi, Okazaki, Kazuichi
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Sprache:eng
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Zusammenfassung: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.
ISSN:1687-9260
1687-9279
DOI:10.1155/2012/795026