Target intelligence / Profile preview

Tumor-specific T-cell receptor (TCR) (TCR)

Target
TCR
Molecular classification
Receptor, Antigen-recognition receptor, Immunoglobulin superfamily
01

Overview

Tumor-specific T-cell receptors (TCRs) are heterodimeric surface proteins, typically composed of alpha (α) and beta (β) chains, that mediate the recognition of specific peptide fragments presented by Major Histocompatibility Complex (MHC) molecules (UniProt, 2024). Unlike Chimeric Antigen Receptors (CARs) that recognize surface-bound antigens, TCRs can target intracellular proteins—which constitute the majority of the proteome—after they are processed into peptides and presented on the cell surface (Nature Reviews Drug Discovery, 2021). In oncology, these receptors are engineered or selected to recognize tumor-associated antigens (TAAs) like MAGE-A4 or NY-ESO-1, or patient-specific neoantigens resulting from somatic mutations (NCI Dictionary, 2023). Therapeutic applications include TCR-engineered T-cell (TCR-T) therapy, such as the FDA-approved Afamitresgene autoleucel, and soluble bispecific TCR-based engagers like Tebentafusp (FDA, 2022; FDA, 2024). These therapies allow for the redirection of the immune system against solid tumors that may lack suitable surface targets for traditional antibody-based approaches. However, the clinical utility of TCR-based drugs is restricted by the requirement for specific Human Leukocyte Antigen (HLA) types in patients and the risk of off-target toxicity if the target peptide is shared by healthy tissues (Journal of Hematology & Oncology, 2023).

Other names
Tumor-reactive T-cell receptorNeoantigen-specific TCREngineered T-cell receptorTCR complexMHC-restricted T-cell receptorTumor-specific T-cell receptors recognizing MHC-presented tumor-associated antigens and neoantigens
02

Mechanism of action

TCR-based therapies function by either engineering a patient's own T cells to express a specific TCR (TCR-T therapy) or by using soluble bispecific molecules (ImmTACs) that bridge a TCR-based recognition domain with an anti-CD3 effector domain, thereby inducing T-cell mediated lysis of tumor cells presenting the target MHC-peptide complex (Nature Reviews Drug Discovery, 2021; FDA, 2022).

03

Biological functions

Immune responseAntigen recognitionSignal transductionCell-mediated cytotoxicityT-cell activation
04

Disease associations

CancerSolid tumorsHematological malignancies
05

Safety considerations

Cytokine release syndrome (CRS)Immune effector cell-associated neurotoxicity syndrome (ICANS)On-target off-tumor toxicity due to expression of target antigens in healthy tissuesOff-target toxicity due to TCR cross-reactivity with unrelated peptides (molecular mimicry)HLA downregulation or loss as a mechanism of tumor resistance
06

Interacting drugs

Afamitresgene autoleucel

4 more in the full profile.

07

Biomarkers

HLA-A*02:01 genotypeMAGE-A4 protein expressionNY-ESO-1 protein expressiongp100 protein expressionPRAME protein expressionTumor mutational burden (TMB)Neoantigen load

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