Moving Forward With Biologics in Lupus Nephritis

被引:7
|
作者
Hobeika, Liliane [1 ]
Ng, Lauren [1 ]
Lee, Iris J. [1 ]
机构
[1] Temple Univ, Lewis Katz Sch Med, Sect Nephrol Hypertens & Kidney Transplantat, Philadelphia, PA 19122 USA
关键词
Systemic lupus erythematosus; Lupus nephritis; Clinical trials; Biologics; Experimental therapy; B-CELL DEPLETION; LYMPHOCYTE STIMULATOR LEVELS; TUMOR-NECROSIS-FACTOR; STAGE RENAL-DISEASE; RHEUMATOID-ARTHRITIS; DOUBLE-BLIND; MONOCLONAL-ANTIBODY; MURINE LUPUS; PLASMA-CELLS; EMERGING THERAPIES;
D O I
10.1053/j.ackd.2019.08.008
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The majority of patients with systemic lupus erythematosus develop lupus nephritis (LN) which significantly contributes to increased risks of hospitalizations, ESRD, and death. Unfortunately, treatments for LN have not changed over the past 15 years. Despite continued efforts to elucidate the pathogenesis of LN, no new drugs have yet replaced the standard-of-care regimens of cyclophosphamide or mycophenolate mofetil plus high-dose corticosteroids. The significant limitations of standard-of-care are low complete response rates, risk of flares, and ongoing inflammation in the kidney leading to progressive renal dysfunction. Repeat and prolonged treatments are often needed to control disease, leading to a high level of severe side effects. The development of targeted drugs with better efficacy and safety are desperately needed. The rationale for targeting key immunologic pathways in LN continues to be strongly supported by basic and translational research and has generated the hope and excitement of testing these therapies in human LN. This review provides an overview of biologics studied to date in clinical trials of LN, discusses the potential reasons for their failure, and addresses the challenges moving forward. (C) 2019 by the National Kidney Foundation, Inc. All rights reserved.
引用
收藏
页码:338 / 350
页数:13
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