It is wel females are more immunocompetent than males as evidenced by higher humoral antibody titers, iowered· susceptibility to infection, ~d more efficient graft rejection.Furthermore, females also exhibit a much-higher inc~dence ot ~uto-immune disease. In order to amplify the sensitivity of the responding system, we then elected to study testosterone immunosuppression in a regenerating hemopoietic system which was recovering from the ablative effects of sublethal irradiation.It w~s observed, using ~rradiated mice, that orchidectomy resulted in striking immunoenhancement, where as testosterone treatment produced suppression of the antibody response to S~BC immunization.A possible mechanism for the testosterone effect consisting of a preferential differentiation of the regenerating stem cell population ~long the myeloid pathway was explored. Differential white blood cell counts indicated that testosterone administration can produce a reversal ot the granulocyte:lymphocyte ratio resulting in a marked granulocytosis ~ith acco~panying lymphopenia. Interestingly, in one experiment where testosterone had been observed to induce this reversal of the granulocyte:lymphocyte ratio at eight weeks following irradiation, by 12 week~ the blood picture had returned to normal. However, marked immunosuppression was still evldent in these animals.
3These data have suggested that the immunosuppression pro~uced by testosterone may be the result of a preferential differentiat~on of.the regenerating stem cell population along the myeloid pathway, with a concurrent suppression of lymphocyte production. Furthermore, evidence suggests that there may be a selective sensitivity of one immunocyte subpopulation to testosterone modulation of differentiation.
ANDROGEN-INDUCED IHMUHOSUPPRESSIONby DEBRA ANN WEY~T