Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Curing type 1 diabetes by islet transplantation requires overcoming both allorejection and recurrent autoimmunity. This has been achieved with systemic immunosuppression, but tolerance induction would be preferable. Most islet allotransplant tolerance induction protocols have been tested in nonobese diabetic (NOD) mice, and most have failed. Failure has been attributed to the underlying autoimmunity, assuming that autoimmunity and resistance to transplantation tolerance have a common basis. Out of concern that NOD biology could be misleading in this regard, we tested the hypothesis that autoimmunity and resistance to transplantation tolerance in NOD mice are distinct phenotypes. Unexpectedly, we observed that (NOD x C57BL/6)F(1) mice, which have no diabetes, nonetheless resist prolongation of skin allografts by costimulation blockade. Further analyses revealed that the F(1) mice shared the dendritic cell maturation defects and abnormal CD4(+) T cell responses of the NOD but had lost its defects in macrophage maturation and NK cell activity. We conclude that resistance to allograft tolerance induction in the NOD mouse is not a direct consequence of overt autoimmunity and that autoimmunity and resistance to costimulation blockade-induced transplantation tolerance phenotypes in NOD mice can be dissociated genetically. The outcomes of tolerance induction protocols tested in NOD mice may not accurately predict outcomes in human subjects.

Original publication

DOI

10.4049/jimmunol.171.1.185

Type

Journal article

Journal

Journal of immunology (Baltimore, Md. : 1950)

Publication Date

07/2003

Volume

171

Pages

185 - 195

Addresses

Program in Immunology and Virology, University of Massachusetts Medical School, Worcester, MA 01655, USA.

Keywords

Dendritic Cells, Killer Cells, Natural, CD8-Positive T-Lymphocytes, Bone Marrow Cells, Cells, Cultured, Macrophages, Animals, Mice, Inbred C3H, Mice, Inbred C57BL, Mice, Inbred NOD, Mice, Knockout, Mice, Lymphopenia, Diabetes Mellitus, Type 1, Autoimmune Diseases, Genetic Predisposition to Disease, Membrane Glycoproteins, CD40 Ligand, Receptors, Interleukin-2, Antigens, CD, Genetic Markers, Antibodies, Monoclonal, CD4-CD8 Ratio, Lymphocyte Transfusion, Skin Transplantation, Cell Count, Injections, Intravenous, Crosses, Genetic, Lymphocyte Activation, Cell Adhesion, Cell Differentiation, Cytotoxicity, Immunologic, Transplantation Tolerance, Graft Survival, Homozygote, Female, Male, Immunity, Innate, CD40 Antigens, B7-2 Antigen