Publication | Closed Access
T cell regeneration after allogeneic and autologous bone marrow transplantation
58
Citations
15
References
1983
Year
Cell TherapyImmunologyPathologyImmunotherapyT Cell RegenerationRegenerative MedicineBone Marrow FailureStem Cell TransplantationHematologyGraft SurvivalCell TransplantationT Cell SubsetsTransplantationMarrow TransplantationAutoimmune DiseaseAutoimmunityBlood TransplantationCell BiologyFatal GvhdTransplant RejectionMonoclonal AntibodiesMedicineGraft Rejection
Venous blood T cell phenotypes were analysed with monoclonal antibodies after 11 allogeneic and 17 autologous bone marrow transplants. In seven cases studied in the early regenerative period, cells with a thymocyte phenotype were present in the blood. In the large majority of patients treated with both allografts and autografts there was an imbalance of phenotypic 'helper' and 'suppressor' T cell subsets with initially a relative and later an absolute increase of 'suppressor' T cells. This imbalance was still present at over 250 d in eight out nine cases. Suppressor T cells bearing HLA-Dr antigens were abundant in one case of fatal GVHD but not in another, and were also increased following two autografts. It is concluded that T cell phenotyping is not of diagnostic value in sick patients following bone marrow transplantation when graft-versus-host disease is suspected.
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