Document 0730 DOCN M9590730 TI Immunohistochemical analysis of T cell phenotypes in patients with graft-versus-host disease following allogeneic bone marrow transplantation. DT 9509 AU Diamond DJ; Chang KL; Jenkins KA; Forman SJ; Department of Hematology and Bone Marrow Transplantation, City of; Hope National Medical Center, California, USA. SO Transplantation. 1995 May 27;59(10):1436-44. Unique Identifier : AIDSLINE MED/95288801 AB Allogeneic bone marrow transplantation has become the therapy of choice in many cases of hematologic malignancy. In both matched related donor transplants--and, to a greater degree, in unrelated donor transplant situations--a major complication of the procedure is GVHD. This problem is caused by mature T cells in the graft, which also facilitate engraftment, and mediate an antitumor effect to reduce relapse. In order to further characterize the T cells that are present at the GVHD site of injury, we have studied 134 fresh tissue biopsies using immunohistochemical methods from 50 consecutive ABMT recipients clinically suspected of having acute GVHD. Antibodies specific for T cells, T cell receptor subsets, B cells, and NK cells were used to characterize the lymphocytic infiltrate in the biopsy tissue from GVHD patients. The data showed that the majority of lymphocytes that had infiltrated the epithelium or epidermis were CD3+ T cells. Using antibodies that distinguished the alpha/beta (beta F1) from the gamma/delta TCR (TCR delta 1)-expressing T cells, we observed that the lymphocytic infiltrates from involved tissues of the gastrointestinal tract, skin, and liver are almost exclusively derived from the alpha/beta expressing T cell subset, and are of the memory cell subset of T cells (CD45RO). This is in contrast to some examples from other disease states, in which a significant proportion of the lymphocytes that infiltrate the epidermal layers are of the gamma/delta type. DE Adolescence Adult Biopsy Bone Marrow Transplantation/*ADVERSE EFFECTS CD4-Positive T-Lymphocytes/CYTOLOGY CD8-Positive T-Lymphocytes/CYTOLOGY Gastrointestinal System/CHEMISTRY/PATHOLOGY/ULTRASTRUCTURE Graft vs Host Disease/*ETIOLOGY/*GENETICS Human *Immunohistochemistry Immunologic Memory/IMMUNOLOGY Liver/PATHOLOGY Middle Age Phenotype Receptors, Antigen, T-Cell, alpha-beta/ANALYSIS Skin/CHEMISTRY/PATHOLOGY/ULTRASTRUCTURE Support, U.S. Gov't, P.H.S. T-Lymphocyte Subsets/CYTOLOGY T-Lymphocytes/CHEMISTRY/*METABOLISM JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).