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Complement inhibition in C3 glomerulopathy

期刊

SEMINARS IN IMMUNOLOGY
卷 28, 期 3, 页码 241-249

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.smim.2016.06.002

关键词

Membranoproliferative glomerulonephritis; C3 glomerulopathy; Complement; Dense deposit disease; C3 glomerulonephritis; Eculizumab

资金

  1. Stead Family Department of Pediatrics, Carver College of Medicine, University of Iowa

向作者/读者索取更多资源

C3 glomerulopathy (C3G) describes a spectrum of glomerular diseases defined by shared renal biopsy pathology: a predominance of C3 deposition on immunofluorescence with electron microscopy permitting disease sub-classification. Complement dysregulation underlies the observed pathology, a causal relationship that is supported by well described studies of genetic and acquired drivers of disease. In this article, we provide an overview of the features of C3G, including a discussion of disease definition and a review of the causal role of complement. We discuss molecular markers of disease and how biomarkers are informing our evolving understanding of underlying pathology. Research advances are laying the foundation for complement inhibition as a targeted approach to treatment of C3G. (C) 2016 Elsevier Ltd. All rights reserved.

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