Background <p>Glioblastoma (GBM) is an aggressive brain tumor associated with poor outcome and limited treatment options. Chimeric antigen receptor (CAR) T cells targeting cell surface antigens were shown to induce tumor regression in patients with GBM, although efficacy was transient. To broaden the range of tumor-restricted antigens, we developed CAR T cells targeting Tenascin-C (TNC), a secreted extracellular matrix protein…
Targeting the extracellular matrix with Tenascin-C-specific CAR T cells extends survival in preclinical models of glioblastoma
Journal for ImmunoTherapy of Cancer | | de Sostoa, J., Marinari, E., Pedard, M., Widmer, V., Davanture, S., Schaller, K., Tissot, S., De Palma, M., Wolf, B., Orend, G., Dutoit, V., Migliorini, D.
Topics: brain-cancer, cervical-cancer
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