| Literature DB >> 24565204 |
Mitsuharu Aga1, Satoru Kondo1, Kazunori Yamada2, Naohiro Wakisaka1, Sayaka Yagi-Nakanishi1, Akira Tsuji1, Kazuhira Endo1, Shigeyuki Murono1, Makoto Ito1, Masamichi Muramatsu3, Mitsuhiro Kawano2, Tomokazu Yoshizaki4.
Abstract
We previously reported a case of immunoglobulin (Ig)G4-related immune inflammation in Warthin tumor. Increased serum IgG4 levels and tissue infiltration of IgG4-positive plasma cells are characteristics of IgG4-related disease (IgG4-RD), a newly emerging clinicopathological entity. However, the relationship between IgG4-RD and Warthin tumor remains to be elucidated. We aimed to investigate the involvement of systemic and local IgG4 production and class-switch recombination in Warthin tumor. We examined serum IgG4 levels and also analyzed the involvement of IgG4-positive plasma cells in Warthin tumors (18 cases) compared with those of pleomorphic adenomas (19 cases) as controls. Furthermore, in specimens of Warthin tumors (3 cases), pleomorphic adenomas (2 cases), and IgG4-RDs (2 cases), we examined messenger RNA expression of activation-induced cytidine deaminase, IgG4 germline transcripts and productive IgG4 by reverse transcription polymerase chain reaction. Serum IgG4 levels were increased in 5 of 18 Warthin tumors and not in any of the 19 pleomorphic adenomas. Infiltration of IgG4-positive plasma cells was detected in 4 Warthin tumors and none in the pleomorphic adenomas. Moreover, activation-induced cytidine deaminase, IgG4 germline transcripts, and productive IgG4 messenger RNA were found to be expressed in 2 of 3 Warthin tumors as well as IgG4-RDs by reverse transcription polymerase chain reaction, but not in pleomorphic adenomas. In conclusion, immunoglobulin class switching to IgG4 may be involved in the pathogenesis of Warthin tumor, and it is possible that certain inflammatory background with an immune reaction is involved in the pathogenesis of Warthin tumor.Entities:
Keywords: Class-switch recombination; IgG4-related disease; Warthin tumor
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Year: 2013 PMID: 24565204 DOI: 10.1016/j.humpath.2013.11.012
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466