B lymphocytes are resistant to death receptor 5-induced apoptosis

被引:4
|
作者
Crowder, Roslyn N. [1 ]
Zhao, Hong [2 ]
Chatham, W. Winn [2 ]
Zhou, Tong [2 ]
Carter, Robert H. [3 ]
机构
[1] Penn State Coll Med, Penn State Milton S Hershey Med Ctr, Hershey, PA USA
[2] Univ Alabama, Dept Med, Birmingham, AL USA
[3] Natl Inst Arthrit & Musculoskeletal & Skin Dis, Bethesda, MD USA
关键词
Death receptor 5; B lymphocyte; Systemic lupus erythematosus; Cancer; SYSTEMIC-LUPUS-ERYTHEMATOSUS; CYTOTOXIC LIGAND TRAIL; NF-KAPPA-B; RHEUMATOID-ARTHRITIS; T-CELLS; C-FLIP; MEDIATED APOPTOSIS; TUMOR-CELLS; SYNOVIAL FIBROBLASTS; TUMORICIDAL ACTIVITY;
D O I
10.1016/j.clim.2010.12.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Death Receptor 5 (DR5) induces apoptosis in various types of cells and is a potential therapeutic target. We have investigated whether targeting DR5 could be used to eliminate pathogenic B lymphocytes from systemic lupus erythematosus (SLE) patients. We examined DR5 expression and function on B lymphocytes from healthy controls subjects, SLE patients, and human tonsil. DR5 was expressed similarly on all B cell subpopulations, including resting and activated B cells. Expression of DR5 was equivalent on B cells from SLE patients and healthy subjects. Additionally, DR5 expression was unchanged after B lymphocyte stimulation. However, B cells were resistant to DR5-induced apoptosis, including after in vitro activation. No changes in subsets of B cells were observed in subjects of a trial of CS-1008, an agonist anti-DR5. While DR5 shows promise as a way to selectively eliminate tumor cells and activated synoviocytes, these data suggest DR5 alone cannot be used as a target to remove pathogenic SLE B cells. Published by Elsevier Inc.
引用
收藏
页码:21 / 31
页数:11
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