Priming and effector dependence on insulin B:9-23 peptide in NOD islet autoimmunity

J Clin Invest. 2007 Jul;117(7):1835-43. doi: 10.1172/JCI31368.

Abstract

NOD mice with knockout of both native insulin genes and a mutated proinsulin transgene, alanine at position B16 in preproinsulin (B16:A-dKO mice), do not develop diabetes. Transplantation of NOD islets, but not bone marrow, expressing native insulin sequences (tyrosine at position B16) into B16:A-dKO mice rapidly restored development of insulin autoantibodies (IAAs) and insulitis, despite the recipients' pancreatic islets lacking native insulin sequences. Splenocytes from B16:A-dKO mice that received native insulin-positive islets induced diabetes when transferred into wild-type NOD/SCID or B16:A-dKO NOD/SCID mice. Splenocytes from mice immunized with native insulin B chain amino acids 9-23 (insulin B:9-23) peptide in CFA induced rapid diabetes upon transfer only in recipients expressing the native insulin B:9-23 sequence in their pancreata. Additionally, CD4(+) T cells from B16:A-dKO mice immunized with native insulin B:9-23 peptide promoted IAAs in NOD/SCID mice. These results indicate that the provision of native insulin B:9-23 sequences is sufficient to prime anti-insulin autoimmunity and that subsequent transfer of diabetes following peptide immunization requires native insulin B:9-23 expression in islets. Our findings demonstrate dependence on B16 alanine versus tyrosine of insulin B:9-23 for both the initial priming and the effector phase of NOD anti-islet autoimmunity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoantibodies / immunology
  • Autoimmunity / immunology*
  • Bone Marrow Transplantation
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • Cell Transplantation
  • Cross-Priming / immunology
  • Diabetes Mellitus / genetics
  • Diabetes Mellitus / immunology
  • Diabetes Mellitus / metabolism
  • Diabetes Mellitus / pathology
  • Immunization
  • Insulin / genetics
  • Insulin / immunology*
  • Insulin / metabolism*
  • Islets of Langerhans / immunology*
  • Islets of Langerhans / metabolism*
  • Mice
  • Mice, Inbred NOD
  • Peptide Fragments / genetics
  • Peptide Fragments / immunology*
  • Peptide Fragments / metabolism*
  • Spleen / immunology
  • Spleen / metabolism
  • Spleen / transplantation
  • Survival Rate

Substances

  • Autoantibodies
  • Insulin
  • Peptide Fragments
  • insulin B (9-23)