Membranous nephropathy: Mechanistic insights and therapeutic perspectives

膜性肾病 免疫系统 发病机制 免疫学 肾病综合征 医学 生物信息学 肾小球肾炎 生物 内科学
作者
Meng-Ru Hua,Yanlong Zhao,Junzheng Yang,Liang Zou,Ying‐Yong Zhao,Xia Li
出处
期刊:International Immunopharmacology [Elsevier]
卷期号:120: 110317-110317 被引量:13
标识
DOI:10.1016/j.intimp.2023.110317
摘要

Membranous nephropathy (MN) is one of the most common causes of non-diabetic nephrotic syndrome in adults. About 80% of cases are renal limited (primary MN) and 20% are associated with other systemic diseases or exposures (secondary MN). Autoimmune reaction is the main pathogenic factor of MN, and the discovery of autoantigens including the phospholipase A2 receptor and thrombospondin type-1 domain-containing protein 7A has led to new insights into the pathogenesis, they can induce humoral immune responses led by IgG4 makes them suitable for the diagnosis and monitoring of MN. In addition, complement activation, genetic susceptibility genes and environmental pollution are also involved in MN immune response. In clinical practice, due to the spontaneous remission of MN, the combination of supportive therapy and pharmacological treatment is widely used. Immunosuppressive drugs are the cornerstone of MN treatment, and the dangers and benefits of this approach vary from person to person. In summary, this review provides a more comprehensive review of the immune pathogenesis, interventions and unresolved issues of MN in the hope of providing some new ideas for clinical and scientific researchers in the treatment of MN.
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