Immunotherapy has advanced significantly, with antibody therapies targeting cell surface or soluble antigens like PD-1 and PD-L1. However, many tumor-associated antigens, such as RAS and P53, are intracellular, limiting antibody effectiveness. T cell receptors (TCRs) can target these intracellular antigens via MHC-antigen-peptide (MAP) complexes, but their low affinity often enables tumor immune evasion.
Briefly, BLD1102 is a new ADC platform developed by Biocytogen independently.
TCR-mimic Antibody developed from RenTCRmimic™ mice
Most traditional antibodies target cell surface antigens (PD-1 and PD-L1, etc) or soluble antigens. However, ideal tumor antigens are often intracellular, (RAS, P53, WT1, etc). Endogenous T cell receptor (TCR) can recognize intracellular antigen/HLA complex, i.e. MHC-antigen-peptide, MAP, to activate T cells against tumor cells. But their affinity to the antigen is low, which often leads to tumor immune escape.
Biocytogen's TCR-mimic (TCRm) antibody technology platform is designed for the discovery of TCRm antibodies with high affinity and specificity compared with endogenous TCRs.
Target(s) | Immunization |
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Preclinical | IND |
WT1 |
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NY-ESO-1 |
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KRAS G12V/HLA-A03 |
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KRAS G12V/HLA-A11 |
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GP100 |
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MAGEA4 |
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AFP |
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BIRC5 |
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LMP2 |
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