Abnormal differentiation of thymocytes in mice treated with cyclosporin A

Abstract

Cyclosporin A (CsA) acts as a powerful immunosuppressive agent, and also, when given in repeated doses, can cause T-cell-dependent graft-versus-host disease and organ-specific autoimmune disease in rodents^1–6. This suggests that CsA interferes with the processes governing self-tolerance¹, either by nullifying the activity of T suppressor cells^4,6 or by preventing the deletion of autoreactive T cells during ontogeny in the thymus². We report here that irradiated mice given repeated injections of CsA show striking dysfunction of the thymus. There are two different effects, the first of which is that CsA seems to block the differentiation of immature CD4⁺CD8⁺ thymocytes into mature CD4⁺CD8^- and CD4^-CD8⁺ cells expressing a high density of T-cell receptors and CD3 molecules. Second, CsA-treated mice show incomplete deletion of T cells expressing T-cell receptor molecules reactive to self H–2 I–E molecules.