Inhibition of B cell activating factor (BAFF) in the management of systemic lupus erythematosus (SLE)

被引:48
|
作者
Stohl, William [1 ]
机构
[1] Univ Southern Calif, Div Rheumatol, Dept Med, Keck Sch Med, Los Angeles, CA USA
关键词
APRIL; atacicept; BAFF; BCMA; belimumab; blisibimod; BR3; tabalumab; TACI; NECROSIS-FACTOR FAMILY; LYMPHOCYTE STIMULATOR LEVELS; NZM; 2328; MICE; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; APRIL-DEFICIENT MICE; AUTOIMMUNE-DISEASE; MATURATION ANTIGEN; RHEUMATOID-ARTHRITIS; CRYSTAL-STRUCTURE; TNF RECEPTOR;
D O I
10.1080/1744666X.2017.1291343
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: The anti-BAFF monoclonal antibody, belimumab, was approved 5+ years ago by the US Food and Drug Administration for the treatment of adult SLE patients. Although BAFF is now a proven therapeutic target in SLE, the limited clinical efficacy both in the clinical trials setting and in real-life' experience begs for further therapeutic improvement.Areas covered: In addition to belimumab, three other BAFF antagonists (atacicept, blisibimod, tabalumab) that biologically differ from belimumab are being or have been evaluated in SLE late-stage clinical trials. Literature search was performed using the search words/phrases, BAFF', BLyS', APRIL', BCMA', TACI', BR3', belimumab', atacicept', blisibimod', tabalumab', lupus clinical trial' along with papers from the author's personal library.Expert commentary: The reasons underlying current lack of enthusiasm among clinicians for BAFF antagonism are discussed, and speculation if offered regarding the use of a BAFF antagonist as part of sequential therapy and regarding the utility of individual or pairs of BAFF receptors as therapeutic targets.
引用
收藏
页码:623 / 633
页数:11
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