Shan Li, Lin Ding, Yan-Jiang Yang, Xiang-Dong Yang
{"title":"Telitacicept for minimal change disease.","authors":"Shan Li, Lin Ding, Yan-Jiang Yang, Xiang-Dong Yang","doi":"10.1002/kjm2.12719","DOIUrl":null,"url":null,"abstract":"Minimal change disease (MCD) is a common pathological type of idiopathic nephrotic syndrome. The first-line therapy is prednisone, but steroid-sensitive forms frequently relapse. Telitacicept, a B lymphocyte stimulator and a proliferation-inducing ligand dual inhibitor, has been investigated for several autoimmune diseases. A 44-year-old female presented with edema of both lower extremities for 20 days in July 2020. Urine protein was +++, 24-h urine protein was 5055 mg, and serum albumin was 25.5 g/L; other laboratory test results were unremarkable. The patient received Tripterygium wilfordii, irbesartan, and antihydropic diuretic agents for 2 months. The edema was not completely alleviated. Renal pathology showed no obvious pathological changes. Immunofluorescence revealed no obvious immunofluorescence distribution. Electron microscopy showed a diffuse foot process fusion of the podocytes,","PeriodicalId":49946,"journal":{"name":"Kaohsiung Journal of Medical Sciences","volume":"39 7","pages":"748-749"},"PeriodicalIF":2.7000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kaohsiung Journal of Medical Sciences","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/kjm2.12719","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 1
Abstract
Minimal change disease (MCD) is a common pathological type of idiopathic nephrotic syndrome. The first-line therapy is prednisone, but steroid-sensitive forms frequently relapse. Telitacicept, a B lymphocyte stimulator and a proliferation-inducing ligand dual inhibitor, has been investigated for several autoimmune diseases. A 44-year-old female presented with edema of both lower extremities for 20 days in July 2020. Urine protein was +++, 24-h urine protein was 5055 mg, and serum albumin was 25.5 g/L; other laboratory test results were unremarkable. The patient received Tripterygium wilfordii, irbesartan, and antihydropic diuretic agents for 2 months. The edema was not completely alleviated. Renal pathology showed no obvious pathological changes. Immunofluorescence revealed no obvious immunofluorescence distribution. Electron microscopy showed a diffuse foot process fusion of the podocytes,
期刊介绍:
Kaohsiung Journal of Medical Sciences (KJMS), is the official peer-reviewed open access publication of Kaohsiung Medical University, Taiwan. The journal was launched in 1985 to promote clinical and scientific research in the medical sciences in Taiwan, and to disseminate this research to the international community. It is published monthly by Wiley. KJMS aims to publish original research and review papers in all fields of medicine and related disciplines that are of topical interest to the medical profession. Authors are welcome to submit Perspectives, reviews, original articles, short communications, Correspondence and letters to the editor for consideration.