When highly purified neonatal rat islet tissue, derived after 10 days in vitro, was allografted, it was found to be nonimmunogenic or weakly immunogenic. In contrast, nonislet pancreatic components, derived from the same culture system, transplanted with highly purified islet tissue resulted in rejection in 88% of cases. Extension of the culture period did not result in reduced immunogenicity of the nonislet material. Immunostaining of islet or nonislet tissue from the culture system failed to demonstrate major histocompatibility complex (MHC) class II positive cells in the islet tissue, whereas the presence of MHC class II staining cells in the nonislet components was clearly demonstrable. These results demonstrate that the islet tissue obtained by culture isolation isfree of cells capable of stimulating an allogeneic immune response and are consistent with the hypothesis that the absence of MHC class II positive antigen-presenting cells reduces the immunogenicity of the tissue and enhances the survival of allogeneic grafts.
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Original Articles|
February 01 1989
Allotransplantation of Culture-Isolated Neonatal Rat Islet Tissue: Absence of MHC Class II Positive Antigen-Presenting Cells in Nonimmunogenic Islets
Orion D Hegre;
Orion D Hegre
Department of Cell Biology and Neuroanatomy, University of Minnesota
Minneapolis
the Department of Biology, Macalester College
St. Paul, Minnesota
Department of Pediatrics, University of Kansas Medical Center
Kansas City, Kansas
Department of Surgery, University of British Columbia
Vancouver, British Columbia, Canada
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Robert J Ketchum;
Robert J Ketchum
Department of Cell Biology and Neuroanatomy, University of Minnesota
Minneapolis
the Department of Biology, Macalester College
St. Paul, Minnesota
Department of Pediatrics, University of Kansas Medical Center
Kansas City, Kansas
Department of Surgery, University of British Columbia
Vancouver, British Columbia, Canada
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Heinz Popiela;
Heinz Popiela
Department of Cell Biology and Neuroanatomy, University of Minnesota
Minneapolis
the Department of Biology, Macalester College
St. Paul, Minnesota
Department of Pediatrics, University of Kansas Medical Center
Kansas City, Kansas
Department of Surgery, University of British Columbia
Vancouver, British Columbia, Canada
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Cindy R Eide;
Cindy R Eide
Department of Cell Biology and Neuroanatomy, University of Minnesota
Minneapolis
the Department of Biology, Macalester College
St. Paul, Minnesota
Department of Pediatrics, University of Kansas Medical Center
Kansas City, Kansas
Department of Surgery, University of British Columbia
Vancouver, British Columbia, Canada
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R Mark Meloche;
R Mark Meloche
Department of Cell Biology and Neuroanatomy, University of Minnesota
Minneapolis
the Department of Biology, Macalester College
St. Paul, Minnesota
Department of Pediatrics, University of Kansas Medical Center
Kansas City, Kansas
Department of Surgery, University of British Columbia
Vancouver, British Columbia, Canada
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Janet R Serie;
Janet R Serie
Department of Cell Biology and Neuroanatomy, University of Minnesota
Minneapolis
the Department of Biology, Macalester College
St. Paul, Minnesota
Department of Pediatrics, University of Kansas Medical Center
Kansas City, Kansas
Department of Surgery, University of British Columbia
Vancouver, British Columbia, Canada
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Wayne V Moore
Wayne V Moore
Department of Cell Biology and Neuroanatomy, University of Minnesota
Minneapolis
the Department of Biology, Macalester College
St. Paul, Minnesota
Department of Pediatrics, University of Kansas Medical Center
Kansas City, Kansas
Department of Surgery, University of British Columbia
Vancouver, British Columbia, Canada
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Address correspondence and reprint requests to Orion D. Hegre, Department of Cell Biology and Neuroanatomy, University of Minnesota, 321 Church Street, SE, Minneapolis, MN 55455.
Diabetes 1989;38(2):146–151
Article history
Received:
April 25 1988
Revision Received:
July 12 1988
Accepted:
July 12 1988
PubMed:
2492474
Citation
Orion D Hegre, Robert J Ketchum, Heinz Popiela, Cindy R Eide, R Mark Meloche, Janet R Serie, Wayne V Moore; Allotransplantation of Culture-Isolated Neonatal Rat Islet Tissue: Absence of MHC Class II Positive Antigen-Presenting Cells in Nonimmunogenic Islets. Diabetes 1 February 1989; 38 (2): 146–151. https://doi.org/10.2337/diab.38.2.146
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