Selective Stimulation of T Cell Subsets with Antibody-Cytokine Immune Complexes

Onur Boyman(Scripps Research Institute), Marek Kovář(Scripps Research Institute), Mark P. Rubinstein(Scripps Research Institute), Charles D. Surh(Scripps Research Institute), Jonathan Sprent(Scripps Research Institute)
Science
February 16, 2006
Cited by 867

Abstract

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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