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Insulitis in human diabetes: a histological evaluation of donor pancreases. | LitMetric

Insulitis in human diabetes: a histological evaluation of donor pancreases.

Diabetologia

Department of Immunology, Genetics and Pathology, The Rudbeck Laboratory C11, Clinical Immunology, Uppsala University, Dag Hammarskjölds väg 20, 751 85, Uppsala, Sweden.

Published: February 2017

AI Article Synopsis

  • The study investigated the prevalence of insulitis in individuals with type 2 diabetes using established criteria typically for type 1 diabetes, finding that 28% of type 2 diabetic donors had insulitis.
  • Results indicated that while type 1 diabetic donors showed significant infiltration of CD3 T cells, type 2 diabetic donors primarily had macrophages and neutrophils, lacking the same level of T cell presence.
  • Additionally, type 2 diabetic islets with insulitis demonstrated reduced insulin secretion but maintained dynamic responses, suggesting a complex relationship with insulin dysfunction that didn’t correlate with common health metrics like BMI or autoantibody presence.

Article Abstract

Aims/hypothesis: According to the consensus criteria developed for type 1 diabetes, an individual can be diagnosed with insulitis when ≥ 15 CD45 cells are found within the parenchyma or in the islet-exocrine interface in ≥ 3 islets. The aim of this study was to determine the frequency of individuals with type 2 diabetes fulfilling these criteria with reference to non-diabetic and type 1 diabetic individuals.

Methods: Insulitis was determined by examining CD45 cells in the pancreases of 50, 13 and 44 organ donors with type 2 diabetes, type 1 diabetes and no diabetes, respectively. CD3 cells (T cells) infiltrating the islets were evaluated in insulitic donors. In insulitic donors with type 2 diabetes, the pancreases were characterised according to the presence of CD68 (macrophages), myeloperoxidase (MPO; neutrophils), CD3, CD20 (B cells) and HLA class I hyperstained islets. In all type 2 diabetic donors, potential correlations of insulitis with dynamic glucose-stimulated insulin secretion in vitro or age, BMI, HbA or autoantibody positivity were examined.

Results: Overall, 28% of the type 2 diabetic donors fulfilled the consensus criteria for insulitis developed for type 1 diabetes. Of the type 1 diabetic donors, 31% fulfilled the criteria. None of the non-diabetic donors met the criteria. Only type 1 diabetic donors had ≥ 15 CD3 cells in ≥ 3 islets. Type 2 diabetic donors with insulitis also had a substantial number of CD45 cells in the exocrine parenchyma. Macrophages constituted the largest fraction of CD45 cells, followed by neutrophils and T cells. Of type 2 diabetic pancreases with insulitis, 36% contained islets that hyperstained for HLA class I. Isolated islets from type 2 diabetic donors secreted less insulin than controls, although with preserved dynamics. Insulitis in the type 2 diabetic donors did not correlate with glucose-stimulated insulin secretion, the presence of autoantibodies, BMI or HbA.

Conclusions/interpretation: The current definition of insulitis cannot be used to distinguish pancreases retrieved from individuals with type 1 diabetes from those with type 2 diabetes. On the basis of our findings, we propose a revised definition of insulitis, with a positive diagnosis when ≥ 15 CD3 cells, not CD45 cells, are found in ≥ 3 islets.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518093PMC
http://dx.doi.org/10.1007/s00125-016-4140-zDOI Listing

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