| Literature DB >> 24791699 |
Ning Ma1, He Xiao2, Bernadette Marrero3, Chen Xing2, Xiaoqian Wang2, Mingke Zheng4, Gencheng Han2, Guojiang Chen2, Chunmei Hou2, Beifen Shen2, Yan Li2, Renxi Wang2, Zhenyu Jiang5.
Abstract
Clinical trials suggest that BAFF inhibitors such as atacicept (TACI-IgG) and belimumab (anti-BAFF antibody) could not reduce memory B-cell numbers, although they reduced the numbers of CD20(+) naïve B cells and activated B cells. In the present study, we explored the way to reduce memory B-cell numbers. First, we used TACI-IgG to treat murine lupus. We found that TACI-IgG was effective in reducing mature B cell numbers. Accordingly it controlled the level of the anti-dsDNA antibody in lupus-like mice. In addition, TACI-IgG up-regulated memory B cells in murine lupus. Furthermore, we found that TACI-IgG up-regulated IL-15 expression in lupus-like mice. Thus, the combination of TACI-IgG and anti-IL-15 antibodies was explored to understand their effects on the treatment of murine lupus. Compared to treatments with TACI-IgG or anti-IL-15 alone, the combination of TACI-IgG and anti-IL-15 antibodies efficiently ameliorated murine lupus phenotypes. The study provides hints for the clinical application of BAFF- and IL-15-specific therapeutic agents.Entities:
Keywords: IL-15; Lupus; Memory B cells; TACI-IgG
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Year: 2014 PMID: 24791699 DOI: 10.1016/j.cellimm.2014.03.017
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868