Thy1+ bone marrow cells regulate the induction of murine syngeneic graft-versus-host disease
A syngeneic graft-versus-host disease (GVHD)-like syndrome has been shown to be inducible in some strains of mice after lethal irradiation, reconstitution with syngeneic bone marrow (BM), and treatment with a short course of CsA therapy. Since Thy1+ BM cells have been shown to regulate the developme...
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Veröffentlicht in: | Transplantation 1993-10, Vol.56 (4), p.941-945 |
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description | A syngeneic graft-versus-host disease (GVHD)-like syndrome has been shown to be inducible in some strains of mice after lethal irradiation, reconstitution with syngeneic bone marrow (BM), and treatment with a short course of CsA therapy. Since Thy1+ BM cells have been shown to regulate the development of other experimental autoimmune diseases, it was important to determine their role in the inducibility of syngeneic GVHD (SGVHD) in different strains of mice. Lethally irradiated mice were reconstituted with either syngeneic BM or T cell-depleted syngeneic BM, then treated with CsA or diluent. Removal of Thy1+ cells from BM before reconstitution of an inducible strain, C3H/HeN, exacerbated SGVHD when compared with animals given whole BM cells before CsA treatment. Furthermore, a noninducible strain, C57BL/6 mice, developed SGVHD when reconstituted with T cell-depleted syngeneic BM but not BM before CsA therapy. These results suggest that Thy1+ BM cells may regulate the development of SGVHD, and be of importance in controlling autoreactivity after bone marrow transplantation. |
doi_str_mv | 10.1097/00007890-199310000-00031 |
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S ; JENNINGS, C. D ; CAYWOOD, B. E ; KAPLAN, A. M</creator><creatorcontrib>BRYSON, J. S ; JENNINGS, C. D ; CAYWOOD, B. E ; KAPLAN, A. M</creatorcontrib><description>A syngeneic graft-versus-host disease (GVHD)-like syndrome has been shown to be inducible in some strains of mice after lethal irradiation, reconstitution with syngeneic bone marrow (BM), and treatment with a short course of CsA therapy. Since Thy1+ BM cells have been shown to regulate the development of other experimental autoimmune diseases, it was important to determine their role in the inducibility of syngeneic GVHD (SGVHD) in different strains of mice. Lethally irradiated mice were reconstituted with either syngeneic BM or T cell-depleted syngeneic BM, then treated with CsA or diluent. Removal of Thy1+ cells from BM before reconstitution of an inducible strain, C3H/HeN, exacerbated SGVHD when compared with animals given whole BM cells before CsA treatment. Furthermore, a noninducible strain, C57BL/6 mice, developed SGVHD when reconstituted with T cell-depleted syngeneic BM but not BM before CsA therapy. These results suggest that Thy1+ BM cells may regulate the development of SGVHD, and be of importance in controlling autoreactivity after bone marrow transplantation.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/00007890-199310000-00031</identifier><identifier>PMID: 8105571</identifier><identifier>CODEN: TRPLAU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Antigens, Surface - immunology ; Biological and medical sciences ; Bone Marrow Transplantation - immunology ; Bone marrow, stem cells transplantation. Graft versus host reaction ; Cyclosporine - pharmacology ; Graft vs Host Disease - immunology ; Graft vs Host Disease - pathology ; Inflammation ; Liver - immunology ; Liver - pathology ; Lymphocyte Depletion ; Medical sciences ; Membrane Glycoproteins - immunology ; Mice ; Mice, Inbred C3H ; Mice, Inbred C57BL ; Splenomegaly ; T-Lymphocytes - immunology ; Thy-1 Antigens ; Tongue - immunology ; Tongue - pathology ; Transfusions. Complications. Transfusion reactions. 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S</creatorcontrib><creatorcontrib>JENNINGS, C. D</creatorcontrib><creatorcontrib>CAYWOOD, B. E</creatorcontrib><creatorcontrib>KAPLAN, A. M</creatorcontrib><title>Thy1+ bone marrow cells regulate the induction of murine syngeneic graft-versus-host disease</title><title>Transplantation</title><addtitle>Transplantation</addtitle><description>A syngeneic graft-versus-host disease (GVHD)-like syndrome has been shown to be inducible in some strains of mice after lethal irradiation, reconstitution with syngeneic bone marrow (BM), and treatment with a short course of CsA therapy. Since Thy1+ BM cells have been shown to regulate the development of other experimental autoimmune diseases, it was important to determine their role in the inducibility of syngeneic GVHD (SGVHD) in different strains of mice. Lethally irradiated mice were reconstituted with either syngeneic BM or T cell-depleted syngeneic BM, then treated with CsA or diluent. Removal of Thy1+ cells from BM before reconstitution of an inducible strain, C3H/HeN, exacerbated SGVHD when compared with animals given whole BM cells before CsA treatment. Furthermore, a noninducible strain, C57BL/6 mice, developed SGVHD when reconstituted with T cell-depleted syngeneic BM but not BM before CsA therapy. These results suggest that Thy1+ BM cells may regulate the development of SGVHD, and be of importance in controlling autoreactivity after bone marrow transplantation.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Antigens, Surface - immunology</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Transplantation - immunology</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Cyclosporine - pharmacology</subject><subject>Graft vs Host Disease - immunology</subject><subject>Graft vs Host Disease - pathology</subject><subject>Inflammation</subject><subject>Liver - immunology</subject><subject>Liver - pathology</subject><subject>Lymphocyte Depletion</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins - immunology</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Mice, Inbred C57BL</subject><subject>Splenomegaly</subject><subject>T-Lymphocytes - immunology</subject><subject>Thy-1 Antigens</subject><subject>Tongue - immunology</subject><subject>Tongue - pathology</subject><subject>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><subject>Transplantation, Homologous - immunology</subject><subject>Transplantation, Isogeneic - immunology</subject><issn>0041-1337</issn><issn>1534-6080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1LxDAQhoMo6_rxE4QcxItEk6bpNEcRv0DwojehZNPJbqXbrplW2X9vVtcNhBDmmRnehzGu5JWSFq5lOlBaKZS1Wm1-Il2t9thUGZ2LQpZyn02lzJVQWsMhOyL6SIjRABM2KZU0BtSUvb8u1uqSz_oO-dLF2H9zj21LPOJ8bN2AfFggb7p69EPTd7wPfDnGJtG07ubYYeP5PLowiC-MNJJY9DTwuiF0hCfsILiW8HT7HrO3-7vX20fx_PLwdHvzLLwu7SC8MmUws0zXQSLkHh1YC2ALA1q7zAVvlM7LwocZBjQhAx-yurA5FCUU4PUxu_ibu4r954g0VMuGNjFch_1IFRRSKciyBJZ_oI89UcRQrWKTYq8rJauN2OpfbLUTW_2KTa1n2x3jbIn1rnFrMtXPt3VH3rUhus43tMOSdquN1D9UVoCw</recordid><startdate>19931001</startdate><enddate>19931001</enddate><creator>BRYSON, J. S</creator><creator>JENNINGS, C. D</creator><creator>CAYWOOD, B. E</creator><creator>KAPLAN, A. M</creator><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19931001</creationdate><title>Thy1+ bone marrow cells regulate the induction of murine syngeneic graft-versus-host disease</title><author>BRYSON, J. S ; JENNINGS, C. D ; CAYWOOD, B. E ; KAPLAN, A. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-c158f5b23df0e74cea79977965733a2afc513486cfbefe5f27cf2d694768767c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Antigens, Surface - immunology</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Transplantation - immunology</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Cyclosporine - pharmacology</topic><topic>Graft vs Host Disease - immunology</topic><topic>Graft vs Host Disease - pathology</topic><topic>Inflammation</topic><topic>Liver - immunology</topic><topic>Liver - pathology</topic><topic>Lymphocyte Depletion</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins - immunology</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Mice, Inbred C57BL</topic><topic>Splenomegaly</topic><topic>T-Lymphocytes - immunology</topic><topic>Thy-1 Antigens</topic><topic>Tongue - immunology</topic><topic>Tongue - pathology</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><topic>Transplantation, Homologous - immunology</topic><topic>Transplantation, Isogeneic - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BRYSON, J. S</creatorcontrib><creatorcontrib>JENNINGS, C. D</creatorcontrib><creatorcontrib>CAYWOOD, B. E</creatorcontrib><creatorcontrib>KAPLAN, A. M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BRYSON, J. S</au><au>JENNINGS, C. D</au><au>CAYWOOD, B. E</au><au>KAPLAN, A. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thy1+ bone marrow cells regulate the induction of murine syngeneic graft-versus-host disease</atitle><jtitle>Transplantation</jtitle><addtitle>Transplantation</addtitle><date>1993-10-01</date><risdate>1993</risdate><volume>56</volume><issue>4</issue><spage>941</spage><epage>945</epage><pages>941-945</pages><issn>0041-1337</issn><eissn>1534-6080</eissn><coden>TRPLAU</coden><abstract>A syngeneic graft-versus-host disease (GVHD)-like syndrome has been shown to be inducible in some strains of mice after lethal irradiation, reconstitution with syngeneic bone marrow (BM), and treatment with a short course of CsA therapy. Since Thy1+ BM cells have been shown to regulate the development of other experimental autoimmune diseases, it was important to determine their role in the inducibility of syngeneic GVHD (SGVHD) in different strains of mice. Lethally irradiated mice were reconstituted with either syngeneic BM or T cell-depleted syngeneic BM, then treated with CsA or diluent. Removal of Thy1+ cells from BM before reconstitution of an inducible strain, C3H/HeN, exacerbated SGVHD when compared with animals given whole BM cells before CsA treatment. Furthermore, a noninducible strain, C57BL/6 mice, developed SGVHD when reconstituted with T cell-depleted syngeneic BM but not BM before CsA therapy. These results suggest that Thy1+ BM cells may regulate the development of SGVHD, and be of importance in controlling autoreactivity after bone marrow transplantation.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott</pub><pmid>8105571</pmid><doi>10.1097/00007890-199310000-00031</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Antigens, Surface - immunology Biological and medical sciences Bone Marrow Transplantation - immunology Bone marrow, stem cells transplantation. Graft versus host reaction Cyclosporine - pharmacology Graft vs Host Disease - immunology Graft vs Host Disease - pathology Inflammation Liver - immunology Liver - pathology Lymphocyte Depletion Medical sciences Membrane Glycoproteins - immunology Mice Mice, Inbred C3H Mice, Inbred C57BL Splenomegaly T-Lymphocytes - immunology Thy-1 Antigens Tongue - immunology Tongue - pathology Transfusions. Complications. Transfusion reactions. Cell and gene therapy Transplantation, Homologous - immunology Transplantation, Isogeneic - immunology |
title | Thy1+ bone marrow cells regulate the induction of murine syngeneic graft-versus-host disease |
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