Cell-contact-dependent activation of CD4⁺ T cells by adhesion molecules on synovial fibroblasts

To determine how cell-cell contact with synovial fibroblasts (SF) influence on the proliferation and cytokine production of CD4⁺T cells.

Naïve CD4⁺T cells were cultured with SF from rheumatoid arthritis patients, stimulated by anti-CD3/28 antibody, and CD4⁺T cell proliferation and IFN-γ/IL-17 production were analyzed. To study the role of adhesion molecules, cell contact was blocked by transwell plate or anti-intracellular adhesion molecule-1 (ICAM-1)/vascular cell adhesion molecule-1(VCAM-1) antibody. To study the direct role of adhesion molecules for CD4⁺T cells, CD161⁺or CD161^- naïve CD4⁺T cells were stimulated on plastic plates coated by recombinant ICAM-1 or VCAM-1, and the source of IFN-γ/IL-17 were analyzed.

SF enhanced naïve CD4⁺T cell proliferation and IFN-γ/IL-17 production in cell-contact and in part ICAM-1-/VCAM-1-dependent manner. Plate-coated ICAM-1 and VCAM-1 enhanced naïve CD4⁺T cell proliferation and IFN-γ production, while VCAM-1 efficiently promoting IL-17 production. CD161⁺naïve T cells upregulating LFA-1 and VLA-4 were the major source of IFN-γ/IL-17 upon interaction with ICAM-1/VCAM-1.

CD4⁺T cells rapidly expand and secrete IFN-γ/IL-17 upon cell-contact with SF via adhesion molecules. Interfering with ICAM-1-/VCAM-1 may be beneficial for inhibiting RA synovitis.