Document 0029 DOCN M9550029 TI Phenotypic analysis of donor cells infiltrating the small intestinal epithelium and spleen during graft-versus-host disease. DT 9505 AU Schattenfroh NC; Hoffman RA; McCarthy SA; Simmons RL; Department of Surgery, University of Pittsburgh, Pennsylvania; 15261. SO Transplantation. 1995 Jan 27;59(2):268-73. Unique Identifier : AIDSLINE MED/95141394 AB One of the principal target organs during graft-versus-host disease (GvHD) is the intestinal epithelium, although the reasons for the preferential involvement of particular organs in this disease are not known. This study analyzed the subset distribution of donor and host lymphocytes in the small intestinal epithelium and the spleen during GvHD in a parent (C57BL/6J) into F1 (C57BL/6JxDBA2/J F1) model. While the donor cell population in the spleen consisted of B and T cells, the donor cell population in the intestine contained only T cells during the course of GvHD. These infiltrating donor cells resembled the host intraepithelial lymphocytes (IELs), which are predominantly CD8+ T cells. This subset distribution of donor cells in the intestinal epithelium was remarkable since they originated from a donor splenocyte population containing few CD8+ lymphocytes. In addition, although the injected donor splenic T cells were virtually all alpha/beta TCR+, several months after GvHD induction more than 30% of the donor cells in the intestine were gamma/delta TCR+, thereby resembling the host IELs not only in their expression of CD4 and CD8, but also in their TCR expression. In contrast, no gamma/delta TCR+ donor cells were detectable in the spleen of GvHD mice. The subset distribution of donor and host IELs remained constant throughout the disease, while in the spleen a decrease of both donor and host B cells and a temporary increase of both donor and host CD8+ cells was observed. These findings demonstrate that in a given target organ during GvHD the disease process affects both donor and host lymphoid populations. In addition the different tissue microenvironments eventually lead to donor cell repopulation with a subset distribution similar to the host natural lymphoid population of the particular target organ. DE Animal B-Lymphocyte Subsets/IMMUNOLOGY Comparative Study CD4-CD8 Ratio CD8-Positive T-Lymphocytes/IMMUNOLOGY Disease Models, Animal Epithelium/CYTOLOGY/IMMUNOLOGY Graft vs Host Disease/*IMMUNOLOGY/*PATHOLOGY Intestinal Mucosa/CYTOLOGY/IMMUNOLOGY Intestine, Small/*CYTOLOGY/*IMMUNOLOGY Lymphocyte Subsets/*IMMUNOLOGY Male Mice Mice, Inbred C57BL Mice, Inbred DBA Phenotype Receptors, Antigen, T-Cell, gamma-delta/ANALYSIS/IMMUNOLOGY Spleen/*CYTOLOGY/*IMMUNOLOGY Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. T-Lymphocyte Subsets/IMMUNOLOGY Tissue Donors JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).