Targeted therapies for lupus nephritis: Current perspectives and future directions

被引:4
作者
Jia, Xiuzhi [1 ,2 ,3 ]
Lu, Yuewen [1 ,2 ,3 ]
Zheng, Xunhua [1 ,2 ,3 ]
Tang, Ruihan [1 ,2 ,3 ]
Chen, Wei [1 ,2 ,3 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Nephrol, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, NHC Key Lab Clin Nephrol, Guangzhou 510080, Guangdong, Peoples R China
[3] Guangdong Prov Key Lab Nephrol, Guangzhou 510080, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Lupus nephritis; Molecular targeted therapies; Adaptive immunity; Immunity; Innate; Cytokines; B-LYMPHOCYTE STIMULATOR; DOUBLE-BLIND; MONOCLONAL-ANTIBODY; SAFETY; EFFICACY; ERYTHEMATOSUS; BELIMUMAB; ABATACEPT; RITUXIMAB; EVALUATE;
D O I
10.1097/CM9.0000000000002959
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Lupus nephritis (LN), a severe manifestation of systemic lupus erythematosus, poses a substantial risk of progression to end-stage renal disease, with increased mortality. Conventional therapy for LN relies on broad-spectrum immunosuppressants such as glucocorticoids, mycophenolate mofetil, and calcineurin inhibitors. Although therapeutic regimens have evolved over the years, they have inherent limitations, including non-specific targeting, substantial adverse effects, high relapse rates, and prolonged maintenance and remission courses. These drawbacks underscore the need for targeted therapeutic strategies for LN. Recent advancements in our understanding of LN pathogenesis have led to the identification of novel therapeutic targets and the emergence of biological agents and small-molecule inhibitors with improved specificity and reduced toxicity. This review provides an overview of the current evidence on targeted therapies for LN, elucidates the biological mechanisms of responses and failure, highlights the challenges ahead, and outlines strategies for subsequent clinical trials and integrated immunomodulatory approaches.
引用
收藏
页码:34 / 43
页数:10
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