VSIG4/CRIg directly regulates early CD8⁺ T cell activation through its counter-receptor in a narrow window

T-cell responses are fine-tuned by positive and negative co-signal molecules expressed on immune cells and adjacent tissues. VSIG4 is a newly identified member of the B7 family of ligands, which negatively regulates innate inflammatory and CD4⁺ T cell-mediated responses. However, little is known about the direct effects of VSIG4, which are exerted through an unidentified counter-receptor on CD8⁺ T cells. We investigated the binding of the VSIG4-Ig fusion protein during CD8⁺ T cell activation, and the functional involvement of VSIG4 pathway, using VSIG4-Ig and VSIG4-transfectants. VSIG4-Ig binding to CD8⁺ T cells was temporally observed in the CD44^high phenotype during initial activation. VSIG4-Ig binding was observed earlier than the induction of PD-1, LAG3, and TIM-3, which are immune checkpoint receptors for exhausted CD8⁺ T cells. Immobilized VSIG4-Ig inhibited anti-CD3/CD28 mAb-induced CD8⁺ T cell activation, as indicated by proliferation and IFN-γ production, similar to the downregulation of T-bet and Eomesodermin transcription factors. VSIG4 on FcγR⁺ P815 or specific antigen-presenting E.G7 cells inhibited the generation of effector CD8⁺ T cells, as indicated by proliferation, IFN-γ and TNF-α expression, and granule degradation, compared to parental cells. However, the window for the regulatory function of VSIG4 was narrow and dependent on the strength of TCR (and CD28)-mediated signals. Our results suggested that VSIG4 directly delivers co-inhibitory signals via an as-yet unidentified counter-receptor on activated CD8⁺ T cells. VSIG4-mediated CD8⁺ T cell tolerance might contribute to the steady-state maintenance of homeostasis.