Impact of hyperglycemia on immune cell function: a comprehensive review

Hoyul Lee, Min Ji Kim, In Kyu Lee, Chang Won Hong, Jae-Han Jeon

Research output: Contribution to journalReview articlepeer-review

4 Scopus citations

Abstract

Hyperglycemia, a hallmark of diabetes and various metabolic disorders, has profound implications for immune cell function. The relationship between elevated blood glucose levels and immune cell function is a topic of significant medical interest. In this review, we aim to comprehensively review effects of hyperglycemia on various immune cell types and its clinical implications, particularly T cells, macrophages, natural killer cells, and neutrophils. It aims to consolidate current knowledge on the subject, with a focus on both type 1 and type 2 diabetes, as well as other pathological states where hyperglycemia is a concern. A comprehensive examination of recent studies and clinical data was conducted to assess effects of hyperglycemia on immune cell function. Evidence indicates that hyperglycemia can significantly alter immune cell function, with different diabetic conditions showing varied responses. Roles of key metabolic hormones in regulating T cell function highlight potential therapeutic targets for restoring immune balance. In addition, reprogramming of innate immune cells such as macrophages and natural killer cells under hyperglycemic conditions suggests a complex metabolic–immunological interface. This review will contribute to a better understanding of the link between diabetes, other metabolic disorders, and immune function. By examining recent research and clinical findings, this review will enhance our comprehension of the mechanisms at play and guide future medical strategies for managing and treating conditions associated with hyperglycemia.

Original languageEnglish
Pages (from-to)745-760
Number of pages16
JournalDiabetology International
Volume15
Issue number4
DOIs
StatePublished - Oct 2024

Keywords

  • Hyperglycemia
  • Immune cell function
  • Macrophages
  • Natural killer cells
  • Neutrophils
  • T cells

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