Immunotherapy of Type 1 Diabetes: Where Are We and Where Should We Be Going?

Xunrong Luo, Kevan C. Herold, Stephen D. Miller*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

119 Scopus citations

Abstract

Type 1 diabetes (T1D) is a chronic autoimmune disorder characterized by destruction of insulin-producing pancreatic β cells. Many broad-based immunosuppressive and antigen-specific immunoregulatory therapies have been and are currently being evaluated for their utility in the prevention and treatment of T1D. Looking forward, this review discusses the potential therapeutic use of antigen-specific tolerance strategies, including tolerance induced by " tolerogenic" antigen-presenting cells pulsed with diabetogenic antigens and transfer of induced or expanded regulatory T cells, which have demonstrated efficacy in nonobese diabetic (NOD) mice. Depending on the time of therapeutic intervention in the T1D disease process, antigen-specific immunoregulatory strategies may be employed as monotherapies, or in combination with short-term tolerance-promoting immunoregulatory drugs and/or drugs promoting differentiation of insulin-producing β cells from endogenous progenitors.

Original languageEnglish (US)
Pages (from-to)488-499
Number of pages12
JournalImmunity
Volume32
Issue number4
DOIs
StatePublished - Apr 2010

Funding

This work was supported in part by the National Institutes of Health (NIH) Career Award 1K08DK070029 (X.L.), the Type 1 Diabetes Pathfinder Award DP2DK083099 (X.L.), and the Juvenile Diabetes Research Foundation Regular Research Grant 1-2007-1005 (S.D.M and X.L.).

Keywords

  • Cellimmuno
  • Humdisease

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology
  • Infectious Diseases

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