| Literature DB >> 34071896 |
Ling-Sai Chang1, Hong-Ren Yu1, Chiao-Lun Chu1, Kuang-Den Chen2, Ying-Hsien Huang1, Mindy Ming-Huey Guo1, Ken-Pen Weng3,4,5, Ho-Chang Kuo1.
Abstract
The Fc gamma receptor family contains several activating receptors and the only inhibitory receptor, FcγR2B. In this study, we investigated the dynamic methylation change of FcγR2B in different stages of Kawasaki disease (KD). We enrolled a total of 116 participants, which included patients with febrile diseases as controls and KD patients. Whole blood cells of KD patients were collected prior to intravenous immunoglobulin (IVIG) treatment (KD1), three to seven days after IVIG (KD2), three weeks after IVIG treatment (KD3), six months after IVIG (KD4), and one year after IVIG treatment (KD5). In total, 76 KD patients provided samples in every stage. Leukocytes of controls were also recruited. We performed DNA extraction and pyrosequencing. FcγR2B methylation levels were higher in KD3 compared to both the controls and KD1. A significantly higher methylation of FcγR2B was found in KD5 when compared with KD1. FcγR2B methylation levels in the IVIG-resistant group were lower than those in the IVIG-responsive group at KD1-3 (p = 0.004, 0.004, 0.005 respectively). This study is the first to report the dynamic change of FcγR2B methylation and to demonstrate long-term hypermethylation one year after disease onset. Hypomethylation of FcγR2B is associated with IVIG resistance.Entities:
Keywords: FcγR2B methylation; IVIG resistance; Kawasaki disease
Year: 2021 PMID: 34071896 DOI: 10.3390/jcm10112347
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241