BLyS and APRIL form biologically active heterotrimers that are expressed in patients with systemic immune-based rheumatic diseases

被引:204
作者
Roschke, V
Sosnovtseva, S
Ward, CD
Hong, JS
Smith, R
Albert, V
Stohl, W
Baker, KP
Ullrich, S
Nardelli, B
Hilbert, DM
Migone, TS
机构
[1] Human Genome Sci, Dept Preclin Dev, Rockville, MD 20850 USA
[2] Human Genome Sci, Dept Antibody Dev, Rockville, MD 20850 USA
[3] Human Genome Sci, Dept Preclin Discovery, Rockville, MD 20850 USA
[4] Human Genome Sci, Dept Prot Dev, Rockville, MD 20850 USA
[5] Div Rheumatol, Dept Med, Los Angeles, CA 90033 USA
[6] Univ So Calif, Med Ctr, Los Angeles, CA 90033 USA
[7] Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USA
关键词
D O I
10.4049/jimmunol.169.8.4314
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BLyS and APRIL are two members of the TNF superfamily that are secreted by activated myeloid cells and have costimulatory activity on B cells. BLyS and APRIL share two receptors, TACI and BCMA, whereas a third receptor, BAFF-R, specifically binds BLyS. Both BLyS and APRIL have been described as homotrimeric molecules, a feature common to members of the TNF superfamily. In this study, we show that APRIL and BLyS can form active heterotrimeric molecules when coexpressed and that circulating heterotrimers are present in serum samples from patients with systemic immune-based rheumatic diseases. These findings raise the possibility that active BLyS/APRIL heterotrimers may play a role in rheumatic and other autoimmune diseases and that other members of the TNF ligand superfamily may also form active soluble heterotrimers.
引用
收藏
页码:4314 / 4321
页数:8
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