Acceleration of apoptosis in CD4+CD8+ thymocytes by rapamycin accompanied by increased CD4+CD25+ T cells in the periphery

Background Rapamycin (Raps) is an immunosuppressant that is used in patients and animal models to control allograft rejection. Its mechanisms of action are not fully understood. In this article, the authors have investigated the effects of therapeutic doses of Rapa on both thymic and peripheral T-cell populations in the adult rat. Methods. The therapeutic dosage of Rapa was optimized using cardiac transplantation between LEW and DA rats. Thymic morphology was assessed by hematoxylin-eosin staining. Flow cytometric analysis was performed to analyze T-cell phenotype and apoptosis. T-cell receptor (TCR)-mediated T-cell responsiveness was evaluated by (3)[H]-thymidine deoxyribose incorporation. Results. Rapa induced atrophy in the thymus but not in peripheral lymphoid organs. Moreover, fibrosis occurred in thymus that was long-lasting after Rapa withdrawal. In animals treated with Rapa, there was a significant reduction in CD4(+)CD8(+) thymocytes caused by accelerated apoptosis, whereas CD4(-)CD8(-), CD4(+)CD8(-), and CD8(+)CD4(-) populations remained unaffected. In contrast, the cellularity of the periphery lymphoid organs was not altered. Within the CD4(+) thymocyte population, CD4(+)CD25(+) thymocytes were resistant to Rapa-accelerated apoptosis, and in the periphery, the ratio of CD4(+)CD25(+) to CD4(+)CD25(-) T cells was increased. Notably, the peripheral CD4(+)CD25(+) T cells were hyporesponsive to TCR-mediated activation. Conclusions. The resistance of the peripheral CD4(+)CD25(+) T cells to Rapa treatment might contribute to its immunosuppressive action. The long-term effects of Rapa on thymus atrophy and thymocyte development requires consideration with respect to its clinical application.