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TIM-3, LAG-3, or 2B4 gene disruptions increase the anti-tumor response of engineered T cells

20

Citations

56

References

2024

Year

Abstract

These results highlight that TIM-3, LAG-3, and 2B4 disruptions increase the therapeutic benefit of tumor specific cellular products and suggest distinct, non-redundant roles for IRs in anti-tumor responses.

References

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