单克隆抗体
免疫系统
CD8型
体内
T细胞
生物
细胞生物学
抗体
化学
免疫学
细胞因子
分子生物学
细胞毒性T细胞
体外
生物化学
生物技术
作者
Onur Boyman,Marek Kovář,Mark P. Rubinstein,Charles D. Surh,Jonathan Sprent
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2006-02-16
卷期号:311 (5769): 1924-1927
被引量:855
标识
DOI:10.1126/science.1122927
摘要
Interleukin-2 (IL-2), which is a growth factor for T lymphocytes, can also sometimes be inhibitory. Thus, the proliferation of CD8 + T cells in vivo is increased after the injection of a monoclonal antibody that is specific for IL-2 (IL-2 mAb), perhaps reflecting the removal of IL-2–dependent CD4 + T regulatory cells (T regs). Instead, we show here that IL-2 mAb augments the proliferation of CD8 + cells in mice simply by increasing the biological activity of preexisting IL-2 through the formation of immune complexes. When coupled with recombinant IL-2, some IL-2/IL-2 mAb complexes cause massive (>100-fold) expansion of CD8 + cells in vivo, whereas others selectively stimulate CD4 + T regs. Thus, different cytokine-antibody complexes can be used to selectively boost or inhibit the immune response.
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