Anti-CD38 autoimmunity in children with newly diagnosed type 1 diabetes mellitus

C Pupilli1, A Antonelli, L Iughetti

  • 1Endocrinology Unit, Azienda Ospedaliera Careggi and University of Florence, Italy.

Insights

Autoimmunity against CD38 is linked to new cases of type 1 diabetes mellitus (DM1) in children. This CD38 autoimmunity increases and persists over time in children with DM1.

Area of Science:

  • Immunology
  • Endocrinology
  • Pediatrics

Background:

  • Type 1 diabetes mellitus (DM1) is an autoimmune disease.
  • CD38 is a protein expressed in human islets, a potential target in autoimmune responses.
  • Understanding autoimmune targets in DM1 is crucial for developing targeted therapies.

Purpose of the Study:

  • To investigate the presence and significance of anti-CD38 autoantibodies in children with newly-diagnosed type 1 diabetes mellitus.
  • To determine if anti-CD38 autoimmunity is associated with the development or progression of DM1 in pediatric patients.

Main Methods:

  • Serum samples from 270 children with newly-diagnosed DM1 and 179 healthy controls were analyzed for anti-CD38 autoantibodies using Western blot.
  • Follow-up samples were collected from 126 diabetic children after 15 months.
  • Statistical analyses, including chi-squared tests and correlation analysis, were performed.

Main Results:

  • Anti-CD38 autoantibodies were detected in 4.4% of children with DM1, significantly higher than in controls (0.6%, p <0.016).
  • No phenotypic differences were observed between anti-CD38 positive and negative patients.
  • A positive correlation (r = 0.46, p <0.0001) was found between antibody titers at diagnosis and follow-up, with new cases of autoimmunity emerging over time.

Conclusions:

  • An autoimmune reaction against CD38 is associated with newly-diagnosed type 1 diabetes mellitus in children.
  • CD38 autoimmunity appears to increase and persist in children with DM1 over time.
  • These findings suggest CD38 as a potential target in the autoimmune process of pediatric DM1.
Abstract

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