| Literature DB >> 18533277 |
Ann Kari Lefvert1, Yaofeng Zhao, Ryan Ramanujam, Shuyang Yu, Ritva Pirskanen, Lennart Hammarström.
Abstract
In order to investigate the potential involvement of PTPN22 R620W in the pathogenesis of myasthenia gravis (MG), we performed a case-control study including 409 Swedish MG patients and 1557 normal controls. The W620 variant was significantly overrepresented in patients (odds ratio, 1.52; 95% confidence interval, 1.21-1.90; p=0.00027). Incubation of patient (n=100) derived PBMC cells with the autoantigen, the acetylcholine receptor, resulted in a significantly higher number of cells producing anti-AChR antibodies and IL-2 in W620 carriers, suggesting that PTPN22 W620 may be a loss-of-function variant in MG.Entities:
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Year: 2008 PMID: 18533277 DOI: 10.1016/j.jneuroim.2008.04.004
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478