The regulation of immunoglobulin synthesis after HLA-identical bone marrow transplantation: VI. Differential rates of maturation of distinct functional groups within lymphoid subpopulations in patients after human marrow grafting

Abstract

This investigation uses different polyclonal activators of in vitro immunoglobulin production to elicit immunoregulatory profiles of B cells, T cells, T4 cells, and T8 cells from 25 recipients (13 with and 12 without chronic graft-v-host disease [GVHD]) after HLA-identical marrow transplantation for aplastic anemia or hematologic malignancy. Pokeweed mitogen, Epstein-Barr virus, herpes simplex type 1 virus, and tetanus toxoid were used to induce immunoglobulin production as measured a by plaque assay. Multiple defects in the various lymphoid subsets were found in both groups of patients. There was defective B cell function, lack of T cell or T4 cell subset helper activity, and increased T cell, T4 cell, or T8 cell suppressor activity after stimulation with the various activators. Inconsistent B, T, T4, and T8 cell functions in the marrow graft recipients provide evidence for (1) different functional groups of cells within each subset responsive to different polyclonal activators; (2) a spectrum of immune capabilities within each phenotypic lineage; (3) different patterns of immune reconstitution for each lymphocyte subset after marrow grafting; and (4) chronic GVHD altering recovery of in vitro functional responses to the different polyclonal activators.