Interleukin-21 is critically required in autoimmune and allogeneic responses to islet tissue in murine models

HM McGuire, S Walters, A Vogelzang, CMY Lee… - Diabetes, 2011 - Am Diabetes Assoc
HM McGuire, S Walters, A Vogelzang, CMY Lee, KE Webster, J Sprent, D Christ, S Grey
Diabetes, 2011Am Diabetes Assoc
OBJECTIVE Type 1 diabetes is an incurable chronic autoimmune disease. Although
transplantation of pancreatic islets may serve as a surrogate source of insulin, recipients are
subjected to a life of immunosuppression. Interleukin (IL)-21 is necessary for type 1 diabetes
in NOD mice. We examined the efficacy of an IL-21–targeted therapy on prevention of
diabetes in NOD mice, in combination with syngeneic islet transplantation. In addition, we
assessed the role of IL-21 responsiveness in islet allograft rejection in mouse animal …
OBJECTIVE
Type 1 diabetes is an incurable chronic autoimmune disease. Although transplantation of pancreatic islets may serve as a surrogate source of insulin, recipients are subjected to a life of immunosuppression. Interleukin (IL)-21 is necessary for type 1 diabetes in NOD mice. We examined the efficacy of an IL-21–targeted therapy on prevention of diabetes in NOD mice, in combination with syngeneic islet transplantation. In addition, we assessed the role of IL-21 responsiveness in islet allograft rejection in mouse animal models.
RESEARCH DESIGN AND METHODS
NOD mice were treated with IL-21R/Fc, an IL-21–neutralizing chimeric protein. This procedure was combined with syngeneic islet transplantation to treat diabetic NOD mice. Survival of allogeneic islet grafts in IL-21R–deficient mice was also assessed.
RESULTS
Evidence is provided that IL-21 is continually required by the autoimmune infiltrate, such that insulitis was reduced and reversed and diabetes inhibited by neutralization of IL-21 at a late preclinical stage. Recovery from autoimmune diabetes was achieved by combining neutralization of IL-21 with islet transplantation. Furthermore, IL-21–responsiveness by CD8+ T-cells was sufficient to mediate islet allograft rejection.
CONCLUSIONS
Neutralization of IL-21 in NOD mice can inhibit diabetes, and when paired with islet transplantation, this therapeutic approach restored normoglycemia. The influence of IL-21 on a graft-mounted immune response was robust, since the absence of IL-21 signaling prevented islet allograft rejection. These findings suggest that therapeutic manipulation of IL-21 may serve as a suitable treatment for patients with type 1 diabetes.
Am Diabetes Assoc