Target intelligence / Profile preview

Glutamate decarboxylase 65-specific T-cell receptor (GAD65-specific TCR) (GAD65-specific TCR)

Target
GAD65-specific TCR
Molecular classification
Receptor, T-cell receptor complex, Antigen-specific receptor
01

Overview

Glutamate decarboxylase 65-specific T-cell receptors (GAD65-specific TCRs) are specialized protein complexes on T-lymphocytes that recognize peptides from the GAD65 enzyme (encoded by the GAD2 gene) when presented by Major Histocompatibility Complex (MHC) molecules, particularly HLA-DR4 (PMID: 14633806). GAD65 is a primary autoantigen in Type 1 Diabetes (T1D) and Stiff-Person Syndrome, where it triggers an autoimmune response leading to the destruction of pancreatic beta cells or neurological dysfunction (PMID: 21903792). These TCRs are the primary mediators of the pathogenic cellular immune response in T1D, making them high-priority targets for antigen-specific immunotherapies. Current therapeutic strategies include the use of GAD65-based vaccines, such as GAD-alum (Diamyd), which aim to induce immune tolerance and preserve endogenous insulin production (PMID: 21714644). Additionally, researchers are exploring the engineering of regulatory T-cells (Tregs) with GAD65-specific TCRs to provide localized immunosuppression within the pancreatic environment (PMID: 33106333). Monitoring the frequency of T-cells expressing these receptors serves as a critical biomarker for disease progression and therapeutic efficacy in clinical trials.

Other names
GAD2-specific T-cell receptorGAD-65 TCRGlutamate decarboxylase 2-specific T-cell receptorGAD65-reactive T-cell receptor
02

Mechanism of action

Antigen-specific immune modulation through the induction of peripheral tolerance, expansion of regulatory T-cells, or desensitization of autoreactive T-lymphocytes.

03

Biological functions

Immune responseAntigen recognitionT-cell activationAutoimmunity
04

Disease associations

Type 1 diabetes mellitusStiff-person syndromeAutoimmune diseaseLatent autoimmune diabetes in adults (LADA)
05

Safety considerations

Potential for accelerated beta-cell destructionSystemic hypersensitivityCytokine release syndrome in cell-based therapiesOff-target immune suppression
06

Interacting drugs

GAD-alum (Diamyd)

2 more in the full profile.

07

Biomarkers

GAD65 autoantibodies (GADA)GAD65-specific T-cell frequency (tetramer assay)HLA-DRB1*04:01 genotypeC-peptide levels

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