APRIL and TALL-I and receptors BCMA and TACI: system for regulating humoral immunity

被引:316
作者
Yu, G
Boone, T
Delaney, J
Hawkins, N
Kelley, M
Ramakrishnan, M
McCabe, S
Qiu, W
Kornuc, M
Xia, XZ
Guo, J
Stolina, M
Boyle, WJ
Sarosi, I
Hsu, HL
Senaldi, G
Theill, LE
机构
[1] Amgen Inc, Dept Inflammat, Thousand Oaks, CA 91320 USA
[2] Amgen Inc, Dept Proc Sci, Thousand Oaks, CA 91320 USA
[3] Amgen Inc, Dept Prot Chem, Thousand Oaks, CA 91320 USA
[4] Amgen Inc, Dept Pharmacol & Pathol, Thousand Oaks, CA 91320 USA
关键词
D O I
10.1038/79802
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We report that the tumor neurosis factor homolog APRIL (a proliferation-inducing ligand) stimulates in vitro proliferation of primary B and T cells and increases spleen weight due to accumulation of B cells in vivo. APRIL functions via binding to BCMA (B cell maturation antigen) and TACI (transmembrane activator and CAML-interactor) and competes with TALL-I (also called BLyS or BAFF) for receptor binding. Soluble BCMA and TACI specifically prevent binding of APRIL and block APRIL-stimulated proliferation of primary B cells. BCMA-Fc also inhibits production of antibodies against keyhole limpet hemocyanin and Pneumovax in mice, indicating that APRIL and/or TALL-I signaling via BCMA and/or TACI are required for generation of humoral immunity. Thus, APRIL-TALL-I and BCMA-TACI form a two ligands-two receptors pathway involved in stimulation of B and T cell function.
引用
收藏
页码:252 / 256
页数:5
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