このエントリーをはてなブックマークに追加
ID 61950
FullText URL
fulltext.pdf 3.09 MB
Author
Nishikori, Asami Division of Pathophysiology, Okayama University Graduate School of Health Sciences
Nishimura, Yoshito Department of General Medicine, Okayama University Hospital ORCID publons researchmap
Shibata, Rei Department of Pathology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
Ohshima, Koh-Ichi Department of Ophthalmology, National Hospital Organization Okayama Medical Center
Gion, Yuka Division of Pathophysiology, Okayama University Graduate School of Health Sciences Kaken ID researchmap
Ikeda, Tomoka Department of Pathology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
Nishimura, Midori Filiz Department of Pathology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
Yoshino, Tadashi Department of Pathology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences Kaken ID publons researchmap
Sato, Yasuharu Division of Pathophysiology, Okayama University Graduate School of Health Sciences ORCID Kaken ID researchmap
Abstract
Immunoglobulin G4-related disease (IgG4-RD) is a systemic disorder characterized by tissue fibrosis and intense lymphoplasmacytic infiltration, causing progressive organ dysfunction. Activation-induced cytidine deaminase (AID), a deaminase normally expressed in activated B-cells in germinal centers, edits ribonucleotides to induce somatic hypermutation and class switching of immunoglobulin. While AID expression is strictly controlled under physiological conditions, chronic inflammation has been noted to induce its upregulation to propel oncogenesis. We examined AID expression in IgG4-related ophthalmic disease (IgG4-ROD; n = 16), marginal zone lymphoma with IgG4-positive cells (IgG4+ MZL; n = 11), and marginal zone lymphoma without IgG4-positive cells (IgG4- MZL; n = 12) of ocular adnexa using immunohistochemical staining. Immunohistochemistry revealed significantly higher AID-intensity index in IgG4-ROD and IgG4+ MZL than IgG4- MZL (p < 0.001 and = 0.001, respectively). The present results suggest that IgG4-RD has several specific causes of AID up-regulation in addition to inflammation, and AID may be a driver of oncogenesis in IgG4-ROD to IgG4+ MZL.
Keywords
activation-induced cytidine deaminase
IgG4-related disease
IgG4-positive marginal zone lymphoma
Published Date
2021-04-15
Publication Title
International Journal of Molecular Sciences
Volume
volume22
Issue
issue8
Publisher
MDPI
Start Page
4083
ISSN
1422-0067
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
File Version
publisher
PubMed ID
NAID
DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.3390/ijms22084083
License
https://creativecommons.org/licenses/by/4.0/