T cell Ig and mucin domain (TIM)-4 is preferentially expressed on antigen-presenting cells, and its counter-ligand, TIM-1, is thought to deliver co-stimulating signals to T cells. However, the physiological functions of TIM-4 remain unclear. Here, we demonstrate that TIM-4 inhibits naive T cell activation through a ligand other than TIM-1. The inhibitory effect of TIM-4 was specific to naive T cells which do not express TIM-1, and the effect disappeared in pre-activated T cells. Conversely, antibody-mediated blockade of TIM-4 in vivo substantially suppressed T cell-mediated inflammatory responses despite enhanced generation of antigen-specific T cells. Furthermore, treatment with anti-TIM-4 reduced the inflammatory responses developed in mice that were adoptively transferred with antigen-primed T cells. These results suggest that TIM-4 exerts bimodal functions depending on the activation status of T cells. © The Japanese Society for Immunology. 2008. All rights reserved.
CITATION STYLE
Mizui, M., Shikina, T., Arase, H., Suzuki, K., Yasui, T., Rennert, P. D., … Kikutani, H. (2008). Bimodal regulation of T cell-mediated immune responses by TIM-4. International Immunology, 20(5), 695–708. https://doi.org/10.1093/intimm/dxn029
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