利格列汀
医学
二肽基肽酶-4
自身抗体
大疱性类天疱疮
二肽基肽酶
类天疱疮
抗体
胃肠病学
抗原
糖尿病
免疫学
皮肤病科
内科学
内分泌学
2型糖尿病
化学
酶
生物化学
作者
Mei Suezawa,Teruki Dainichi,Yo Kaku,Maiko Izumi,Koki Kataoka,Norito Ishii,Hiroshi Koga,Kentaro Izumi,Wataru Nishie
标识
DOI:10.1111/1346-8138.16061
摘要
Dipeptidyl peptidase 4 inhibitors (DPP-4i) are associated with an increased risk of developing bullous pemphigoid (BP) in patients with diabetes. Autoantibodies targeting epitopes on the processed BP180, 120-kDa (LAD-1), and 97-kDa (LABD97) linear immunoglobulin (Ig)A dermatosis antigens are the major autoantibodies in DPP-4i-associated BP. However, no case of mucous membrane pemphigoid (MMP) developing during treatment with DPP-4i has been reported. We report a case of MMP associated with DPP-4i. A man in his late 70s presented with oral mucous membrane erosion and a few blisters on his upper chest and back. He had used linagliptin for diabetes for over 1 year when he presented. The immunological characteristics were similar to DPP4i-associated BP: higher reactivity to LAD-1 and LABD97 than to the full-length BP180. The aphthae achieved remission after oral linagliptin was replaced with sitagliptin. However, 6 months later, the aphthae relapsed and any DPP-4i was discontinued. The aphthae disappeared, and now he is completely free from lesions associated with MMP. This case suggests that the DPP-4i may have shared roles in the production of IgG antibodies to LAD-1 or to LABD97 in the pathogenesis of DPP-4i-associated BP and MMP. Our case highlights the possibility of overlooking the mild MMP in DPP-4i-treated diabetes patients with mucosal lesions.
科研通智能强力驱动
Strongly Powered by AbleSci AI