| Literature DB >> 19857863 |
Yuki Fujii1, Hiroki Kawamura, Toshihiko Kawamura, Yasuhiro Kanda, Hiroaki Matsumoto, Takahiro Kobayashi, Takashi Yamamoto, Takashi Aoyama, Toru Abo.
Abstract
Severe hepatic injury is induced by Concanavalin A (Con A) administration in mice, the major effector cells being CD4(+) T cells, NKT cells and macrophages. Since autologous lymphocyte subsets are associated with tissue damage, Con A-induced hepatic injury is considered to be autoimmune hepatitis. However, it has remained to be investigated how autoantibodies and B-1 cells are responsible for this phenomenon. In this study, it was demonstrated that autoantibodies which were detected using Hep-2 cells in immunofluorescence tests and using double-strand (ds) DNA in the ELISA method, appeared after Con A administration (a peak at day 14). Moreover, autoantibody-producing B220(low) cells (i.e., B-1 cells) also appeared at this time. Purified B220(low) cells were found to have a potential to produce autoantibodies. These results suggest that Con A-induced hepatic injury indeed includes the mechanism of autoimmune hepatitis.Entities:
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Year: 2010 PMID: 19857863 DOI: 10.1016/j.cellimm.2009.09.009
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868