Tumor associated macrophages (TAMs) are a significant component of all solid tumors and act as a major barrier to T cell recruitment and activation.
TAMs are associated with disease progression, metastasis, and therapy resistance. Our multi-omic analysis defines subsets of TAMs as key drivers of tumor progression and immune suppression across solid tumors.
Our CAR-engineered monocytes remove specific subsets of TAMs across solid tumors. By eliminating these targets, we enable T cell recruitment, activation and durable responses in solid tumors.
CAR-monocytes overcome a fundamental barrier in solid tumors by leveraging the innate tumor-homing properties of monocytes to efficiently infiltrate the tumor microenvironment, enabling effective therapeutic
Engineered specifically to survive and operate within the hostile microenvironment of solid cancers.
Built on deep myeloid biology, our platform is readily adaptable to target diverse macrophage markers across multiple indications.

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