Cited by 38Diabetes and associated disordersEndoplasmic Reticulum Stress and DiseasePancreatic function and diabetes

Setting the Stage for Islet Autoimmunity in Type 2 Diabetes: Obesity-Associated Chronic Systemic Inflammation and Endoplasmic Reticulum (ER) Stress

Open access
Brooks-Worrell, Barbara M., Palmer, Jerry P.·2019·Diabetes Care

Abstract

Islet autoimmunity has been identified as a component of both type 1 (T1D) and type 2 (T2D) diabetes, but the pathway through which islet autoimmunity develops in T1D and T2D may be different. Acknowledging the presence of islet autoimmunity in the pathophysiology of T2D, a historically nonautoimmune metabolic disease, would pave the way for important changes in classifications of and therapeutic options for T2D. In order to fully appreciate the importance of islet autoimmunity in T2D, the underlying mechanisms for immune system activation need to be explored. In this review, we focus on the potential origin of immune system activation (innate and adaptive) leading to the development of islet autoimmunity in T2D.

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Crossref · 10.2337/dc19-0475

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4 of 4 references verified0 citation errors · 0 not checkable

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  • Increased T cell activation by islet proteins has been reported in adults with diabetes mellitus who initially do not require insulin and who lack type 1 diabetes mellitus autoantibodies.

    “Additionally, increased T cell activation by islet proteins has been reported in adults with diabetes mellitus who initially do not require insulin and who lack T1DM autoantibodies65, further complicating the ability to distinguish diabetes mellitus type solely based on autoimmunity.”

    From The epidemiology of type 1 diabetes mellitus in older adults (2025) · cites this paper as [65]

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  • The epidemiology of type 1 diabetes mellitus in older adults

    Tomic, D., Harding, J. L., Jenkins, A. J., Shaw, J. E., & Magliano, D. J. (2025) · Nature Reviews Endocrinology · doi:10.1038/s41574-024-01046-z · Cited by 58 · see citing works

    “Additionally, increased T cell activation by islet proteins has been reported in adults with diabetes mellitus who initially do not require insulin and who lack T1DM autoantibodies 65 , further complicating the ability to distinguish diabetes mellitus type solely based on autoimmunity.”

Authors
Brooks-Worrell, B. M., & Palmer, J. P.
Affiliations
  • Department of Medicine, University of Washington, Seattle, WA
  • University of Washington (US)
Corresponding author
Palmer, Jerry P.
Venue
Diabetes Care
Published
2019-11-12
Volume
42
Issue
12
Pages
2338-2346
ISSN
  • 0149-5992 (ISSN-L)
  • 1935-5548
OpenAlex
W2989857586
Cited by
38
References
4
Citations by year
2026: 3 · 2025: 1 · 2024: 5 · 2023: 5 · 2022: 7 · 2021: 10 · 2020: 7
FWCI
0.80
Type
journal article
Language
en
Open access
Locations
  • Diabetes Care (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institute of Diabetes and Digestive and Kidney Diseases (5R01DK107560, 5R01DK104832)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Endoplasmic Reticulum Stress and Disease
  • Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
Keywords
islet autoimmunity, type 2 diabetes, obesity, chronic systemic inflammation, endoplasmic reticulum stress, innate immunity, adaptive immunity, immune activation
MeSH terms
Animals, Autoantibodies, Diabetes Mellitus, Type 2, Humans, Inflammation, Islets of Langerhans, Obesity, Phenotype, Autoimmunity, Endoplasmic Reticulum Stress

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