Ontology highlight
ABSTRACT: Background
Chimeric antigen receptor (CAR) T-cells are a promising approach in cancer immunotherapy, particularly for treating hematologic malignancies. Yet, their effectiveness is limited when tackling solid tumors, where immune cell infiltration and immunosuppressive tumor microenvironments (TME) are major hurdles. Fibroblast activation protein (FAP) is highly expressed on cancer-associated fibroblasts (CAFs) and various tumor cells, playing an important role in tumor growth and immunosuppression. Aiming to modulate the TME with increased clinical safety and effectiveness, we developed novel small and size-extended immunotheranostic UniCAR target modules (TMs) targeting FAP.Methods
The specific binding and functionality of the αFAP-scFv TM and the size-extended αFAP-IgG4
SUBMITTER: Loureiro LR
PROVIDER: S-EPMC10722841 | biostudies-literature | 2023 Dec
REPOSITORIES: biostudies-literature