There has been disagreement about the ability of exogenous interleukin
-2 (IL-2) to restore responsiveness to lymphocytes from either Trypano
soma cruzi-infected animals or normal individuals co-cultured with thi
s parasite. The discrepancy has been attributed to the use of differen
t strains of mice or T. cruzi isolates, or to the use of lymphoid cell
s from different organs. As T. cruzi inhibits the expression of IL-2 r
eceptors by activated lymphocytes in vitro, we were able to test wheth
er restoration of responsiveness by exogenous IL-2 might depend on the
level of suppression present in the system. Human or mouse lymphocyte
s stimulated with phytohaemagglutinin (PHA) exhibited gradual decrease
s in IL-2 receptor expression, [H-3]thymidine incorporation and IL-2 s
ecretion as the concentration of T. cruzi in the culture increased. Ex
ogenous IL-2 afforded a degree of restoration of both IL-2 receptor ex
pression and [H-3]thymidine uptake which was substantial at the lower,
but very small-if any-at the higher, parasite concentrations tested.
Trypanosoma cruzi could not have competed with the lymphocytes for IL-
2 because it did not bind significant amounts of this cytokine. These
results suggested that the controversy about the corrective effects of
IL-2 may be more apparent than real, reflecting variations in the ext
ent of immunosuppression present in different model systems of T. cruz
i-associated immunosuppression.