Identification of a Type 1 Diabetes-Associated T Cell Receptor Repertoire Signature from the Human Peripheral Blood

Type 1 Diabetes (T1D) is a T-cell mediated disease with a strong immunogenetic HLA dependence. HLA allelic influence on the T cell receptor (TCR) repertoire shapes thymic selection and controls activation of diabetogenic clones, yet remains largely unresolved in T1D. We sequenced the circulating TCRβ chain repertoire from 2250 HLA-typed participants across three cross-sectional cohorts, including T1D individuals, and healthy related and unrelated controls. We found that HLA risk alleles show higher restriction of TCR repertoires in T1D individuals. We leveraged deep learning to identify T1D-associated TCR subsequence motifs that were also observed in independent TCR cohorts residing in pancreas-draining lymph nodes of T1D individuals. Collectively, our data demonstrate T1D-related TCR motif enrichment based on genetic risk, offering a potential metric for autoreactivity and groundwork for TCR-based diagnostics and therapeutics.

• Study Design:
  • Cross-Sectional
• Study Type:
  • Cross-Sectional
  • Genotype
  • Genotype/Expression array
  • Individual-Level Genomic Data
• dbGaP estimated ancestry using GRAF-pop
• Total number of consented subjects: 774
• Subject Sample Telemetry Report (SSTR)

• PubMed

• Primary Phenotype: Type 1 Diabetes

• Principal Investigator
  • Todd M. Brusko. University of Florida, Gainesville, FL, USA.
• Co-Investigator
  • Victor Greiff. University of Oslo, Oslo, Norway.
• Funding Sources
  • 2019PG-T1D011. The Leona M. and Harry B. Helmsley Charitable Trust, New York, NY, USA.
  • P01 AI042288. National Institutes of Health, Bethesda, MD, USA.