Quantitation of immunosuppression by flow cytometric measurement of the capacity of T cells for interleukin-2 production

Background. Methods to quantitate the effects of immunosuppressive drugs on immune reactivity might be helpful for monitoring immunosuppressive treatment. Cyclosporine (CsA) inhibits the induction of cytokine synthesis in T cells, and measurement of interleukin (IL)-2 production might constitute a parameter of this drug's effect.Methods. We determined the percentages of CD4(+) and CD8(+) lymphocytes producing IL-2 upon stimulation by phorbol myristate acetate and calcium ionophore in whole blood culture, using immunostaining of intracytoplasmatic and membrane markers, followed by multiparameter flow cytometry. A total of 38 clinically stable transplant patients on various immunosuppressive protocols were studied.Results. The percentage of CD4(+) T cells producing IL-2 was strongly reduced in patients compared with healthy controls (23% [range, 3-68%] vs. 59.0% [range, 41-70%]; P=0.000035). The percentage of CD4(+) T cells producing IL-2 was negatively correlated with the CSA level (R-c=-0.0821, P=0.00002297) but not with prednisolone or azathioprine doses. Fewer CD8(+) T cells produced IL-2 in transplant patients compared with controls, but the difference failed to reach statistical significance. The percentage of CD8(+) T cells capable of producing IL-2 was inversely correlated to CsA levels (R-c= -0.0375, P=0.0011).Conclusions. These data suggest that the functional effects of CsA in transplant recipients can be quantitatively determined and that the capacity of CD4(+) T cells to produce IL-2 upon stimulation constitutes a functional parameter of CsA effects on the immune system. Prospective studies are required to determine whether this method is useful for clinical monitoring.