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Anti-pS3 T cell receptor (BDC2.5), pCDTCR1 (TCR-YC1039)

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All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.

The overtly diabetogenic character of CD4 T cells bearing the BDC-2.5, BDC-10.1, or BDC-6.9 TCR is shown, for example, in engineered NOD mice expressing retrovirus-encoded TCRs (TCR retrogenics [Rgs]). Unlike TCRs reacting with insulin, IA2β, or GAD65 epitopes, which induced limited or no disease, both BDC-2.5 and BDC-10.1 TCRs induced insulitis and 100% diabetes incidence, with a lower ID₅₀ value in the case of the BDC-10.1 TCR. In comparison, the diabetogenic potential of the BDC-6.9 TCR was less marked in the Rg setting, yet ∼60% of BDC-6.9 TCR–Rg mice became diabetic. In addition, diabetes is accelerated in some BDC-6.9 TCR–transgenic (Tg) mice.

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Details

  • Target
  • pS3
  • Epitope
  • SRLGLWVRME
  • Format
  • Non-Modified TCR
  • Allele
  • H2 class II
  • Targeting Diseases
  • Type 1 diabetes (T1D)
  • Vector Name
  • pCDTCR1
  • Vector Length
  • ~ 8 kb
  • Vector Type
  • Lentiviral vector
  • TCR Clone
  • BDC2.5
  • Host Species
  • Mouse

Target

  • Introduction
  • Multiple studies highlighted the overtly self-reactive T cell repertoire in the diabetes-prone NOD mouse. This autoreactivity has primarily been linked to defects in apoptosis induction during central tolerance. Previous studies suggested that thymus-specific serine protease (TSSP), a putative serine protease expressed by cortical thymic epithelial cells and thymic dendritic cells, may edit the repertoire of self-peptides presented by MHC class II molecules and shapes the self-reactive CD4 T cell repertoire.

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For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.

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