| Literature DB >> 30089633 |
Masahiro Shiokawa1, Yuzo Kodama2, Kiyotoshi Sekiguchi3, Takeshi Kuwada1, Teruko Tomono1, Katsutoshi Kuriyama1, Hajime Yamazaki4, Toshihiro Morita1, Saiko Marui1, Yuko Sogabe1, Nobuyuki Kakiuchi1, Tomoaki Matsumori1, Atsushi Mima1, Yoshihiro Nishikawa1, Tatsuki Ueda1, Motoyuki Tsuda1, Yuki Yamauchi1, Yojiro Sakuma1, Takahisa Maruno1, Norimitsu Uza1, Tatsuaki Tsuruyama5, Tsuneyo Mimori6, Hiroshi Seno1, Tsutomu Chiba1,7.
Abstract
Autoimmune pancreatitis (AIP), a major manifestation of immunoglobulin G4-related disease (IgG4-RD), is an immune-mediated disorder, but the target autoantigens are still unknown. We previously reported that IgG in patients with AIP induces pancreatic injuries in mice by binding the extracellular matrix (ECM). In the current study, we identified an autoantibody against laminin 511-E8, a truncated laminin 511, one of the ECM proteins, in patients with AIP. Anti-laminin 511-E8 IgG was present in 26 of 51 AIP patients (51.0%), but only in 2 of 122 controls (1.6%), by enzyme-linked immunosorbent assay. Because truncated forms of other laminin family members in other organs have been reported, we confirmed that truncated forms of laminin 511 also exist in human and mouse pancreas. Histologic studies with patient pancreatic tissues showed colocalization of patient IgG and laminin 511. Immunization of mice with human laminin 511-E8 induced antibodies and pancreatic injury, fulfilling the pathologic criteria for human AIP. Four of 25 AIP patients without laminin 511-E8 antibodies had antibodies against integrin α6β1, a laminin 511 ligand. AIP patients with laminin 511-E8 antibodies exhibited distinctive clinical features, as the frequencies of malignancies or allergic diseases were significantly lower in patients with laminin 511-E8 antibodies than in those without. The discovery of these autoantibodies should aid in the understanding of AIP pathophysiology and possibly improve the diagnosis of AIP.Entities:
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Year: 2018 PMID: 30089633 DOI: 10.1126/scitranslmed.aaq0997
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956