Selective stimulation of T cell subsets with antibody-cytokine immune complexes

被引:768
作者
Boyman, O
Kovar, M
Rubinstein, MP
Surh, CD
Sprent, J
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[2] St Vincents Hosp, Garvan Inst Med Res, Darlinghurst, NSW 2010, Australia
关键词
D O I
10.1126/science.1122927
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
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.
引用
收藏
页码:1924 / 1927
页数:4
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