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Regulatory T cells in type 1 autoimmune pancreatitis.

Authors :
Uchida K
Kusuda T
Koyabu M
Miyoshi H
Fukata N
Sumimoto K
Fukui Y
Sakaguchi Y
Ikeura T
Shimatani M
Fukui T
Matsushita M
Takaoka M
Nishio A
Okazaki K
Source :
International journal of rheumatology [Int J Rheumatol] 2012; Vol. 2012, pp. 795026. Date of Electronic Publication: 2012 Mar 28.
Publication Year :
2012

Abstract

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.

Details

Language :
English
ISSN :
1687-9279
Volume :
2012
Database :
MEDLINE
Journal :
International journal of rheumatology
Publication Type :
Academic Journal
Accession number :
22536257
Full Text :
https://doi.org/10.1155/2012/795026