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ID 31715
JaLCDOI
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Author
Hirai, Michio
Mizuno, Motowo
Morisue, Yoshiko
Yoshioka, Masao
Shimada, Morizou
Nasu, Junichirou
Shimomura, Hiroyuki
Yamamoto, Kazuhide ORCID Kaken ID publons
Tsuji, Takao
Abstract

Anti-idiotype antibodies (Ab2) play an important role in the homeostasis of immune responses and are related to the development and the disease activity of certain autoimmune diseases. The asialoglycoprotein receptor (ASGPR) is considered one of the target antigens in the pathogenesis of autoimmune chronic active hepatitis (AIH). We previously developed a mouse monoclonal antibody (clone 8D7) which recognizes rat and human ASGPR. In this study, to help investigate the anti-ASGPR antibody-anti-idiotype antibody network in patients with AIH, we developed a syngeneic mouse monoclonal Ab2 to the 8D7 anti-ASGPR antibody (Ab1). One clone, designated as 3C8, tested positive for specific reactivity to 8D7-Ab1 and did not bind to other irrelevant immunoglobulins. By competitive inhibition assays, the binding of 8D7-Ab1 to liver membrane extracts, i.e., the crude antigen preparation, was inhibited by 3C8-Ab2 in a dose-dependent manner, and the binding of 8D7-Ab1 to 3C8-Ab2 was inhibited by the liver membrane extracts. In the immunohistochemical analysis, 3C8-Ab2 blocked the specific staining of sinusoidal margins of rat hepatocytes by 8D7-Ab1. These results suggest that 3C8 anti-idiotype antibody recognizes the specific idiotypic determinants within the antigen-binding site of 8D7-Ab1.

Keywords
anti-idiotype antibody
autoimmune hepatitis
asialoglycoprotein receptor
monoclonall antibody
Amo Type
Article
Publication Title
Acta Medica Okayama
Published Date
2002-06
Volume
volume56
Issue
issue3
Publisher
Okayama University Medical School
Start Page
135
End Page
139
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
English
File Version
publisher
Refereed
True
PubMed ID
Web of Science KeyUT