4.6 Review

Immune modulation in humans: implications for type 1 diabetes mellitus

Journal

NATURE REVIEWS ENDOCRINOLOGY
Volume 10, Issue 4, Pages 229-242

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrendo.2014.2

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Funding

  1. Medical Research Council [MR/J006742/1] Funding Source: Medline
  2. Medical Research Council [MR/J006742/1] Funding Source: researchfish

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Type 1 diabetes mellitus (T1DM) is the result of autoimmune destruction of pancreatic beta cells in genetically predisposed individuals with impaired immune regulation. The insufficiency in the modulation of immune attacks on the beta cells might be partly due to genetic causes; indeed, several of the genetic variants that predispose individuals to T1DM have functional features of impaired immune regulation. Whilst defects in immune regulation in patients with T1DM have been identified, many patients seem to have immune regulatory capacities that are indistinguishable from those of healthy individuals. Insight into the regulation of islet autoimmunity might enable us to restore immune imbalances with therapeutic interventions. In this Review, we discuss the current knowledge on immune regulation and dysfunction in humans that is the basis of tissue-specific immune regulation as an alternative to generalized immune suppression.

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