Effects of substance P on human T cell function and the modulatory role of peptidase inhibitors.

Evidence has been presented for a modulatory role of surface peptidases on substance P-mediated immune responses. In this study, we first characterized the effects of substance P and its carboxy- and amino-terminal fragments on human lymphocyte proliferative responses to investigate whether peptidase inhibitors influence the effects of the neuropeptide. Substance P at 10(-7) M and the carboxy-terminal fragment SP(4-11) slightly enhanced the lymphocyte responses to phytohemagglutinin and concanavalin A. In contrast, the amino-terminal fragment SP(1-4) failed to have any positive effect. However, in the presence of dipeptidylpeptidase IV/CD26 and neutral endopeptidase/CD10 inhibitors (diprotin A and thiorphan, respectively), the effect of substance P on mitogen-induced proliferation was significantly increased. These data support the hypothesis that lymphocyte surface peptidases play a modulatory role in the effects of substance P on T cell function.