Back to Search Start Over

Antibodies to Type IV Collagen Induce Type 1 Autoimmune Pancreatitis.

Authors :
Liu, Qi-cai
Dong, Feng
Pan, Jian-feng
Zhuang, Ze-hao
Gao, Feng
Liu, Guo-zhong
Chen, Qing-quan
Chen, Shu
Weng, Shao-huang
Lin, Li-qing
Chen, Jin-tong
Chen, Min
Wang, Cheng-dan
Lin, Xin-hua
Source :
Inflammation; Apr2016, Vol. 39 Issue 2, p592-600, 9p
Publication Year :
2016

Abstract

Type 1 autoimmune pancreatitis (AIP) is prototypic autoantibody-mediated diseases. Sclerosis accompanied by fiber deposition is generally regarded as the primary lesion in the development of obliterative vasculitis. However, why collagens or their antibodies play a crucial role in the pathogenesis of AIP has not been demonstrated. This study was performed to investigate if anti-collagen type IV antibodies (ACIVAbs) are the key factor of fiber deposition and recruit leukocytes, resulting in obliterative vasculitis in pancreas. Enzyme-linked immunosorbent analyses (ELISA) were used to measure the expression of Col IV and ACIVAbs in serum of patients with and without AIP. In vitro, adhesion and proliferation were determined by human lymphocytes incubated with Col IV and ACIVAbs. In vivo, C57BL0/6 mice were immunized with IgG-ACIVAbs, followed by analysis of clinical phenotype. IgG-ACIVAbs were recognized by the serum specimens from 12 of 22 patients with type 1 AIP, 3 of 9 patients with Crohn's disease, and 2 of 18 patients with pancreatic cancer, but not in healthy controls and acute pancreatitis. In patient's biopsy, ACIVAb staining increased and co-localized with subepithelial IgG4 deposits along the capillary walls and surrounding nerve fibers. In vitro, recombinant IgG-ACIVAbs increased leukocyte adhesion and proliferation. What is more, AIP could be induced in mice by immunization with IgG-ACIVAbs into adult mice. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03603997
Volume :
39
Issue :
2
Database :
Complementary Index
Journal :
Inflammation
Publication Type :
Academic Journal
Accession number :
114149117
Full Text :
https://doi.org/10.1007/s10753-015-0284-0