医学
促炎细胞因子
阿巴塔克普
Toll样受体
共刺激
免疫学
刺激
细胞因子
受体
巨噬细胞
炎症
免疫系统
T细胞
内科学
先天免疫系统
生物
抗体
CD28
生物化学
体外
美罗华
作者
Mark H. Wenink,Kim Santegoets,Andrew M. Platt,Wim B. van den Berg,Piet L. C. M. van Riel,Paul Garside,Timothy R. D. J. Radstake,Iain B. McInnes
标识
DOI:10.1136/annrheumdis-2011-200348
摘要
Objectives We investigated whether Abatacept might reduce proinflammatory cytokine production by macrophages upon contact with cytokine activated T cells and/or stimulation with TLR ligands. Methods Macrophages and cytokine stimulated T cells (Tck) were added together in the presence of Abatacept or a control Ig, with or without TLR ligands. The production of cytokines was determined by luminex. Results Abatacept reduced Tck-induced production of TNFa by macrophages. Tck and TLR ligands synergistically induced the production of proinflammatory cytokines by macrophages, especially IL-12p70. The production of IL-12p70 coincided with the production of IFNg, which were both reduced in the presence of Abatacept. Conclusions Tck induce the production of TNFa by macrophages and facilitate the highly increased production of proinflammatory cytokines in the presence of TLR ligands. Abatacept was shown to potently suppress these pathways suggesting that its role may extend beyond antigen specific T cell mediated effector function.
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