Background <p>Current second-generation CAR T cell products rely on CD28 or 4-1BB costimulatory domains, additions that respectively favor rapid cytolysis or long-term persistence, but rarely both. Preclinical modeling and retrospective analysis have linked CD2–CD58 engagement to superior preclinical and clinical responses, yet the direct contribution of CD2 intracellular signaling remains undefined.</p> Methods <p>We replaced the costimulatory domain of anti-mesothelin (SS1)…
CD2 costimulation bridges potent CAR-induced cytolysis and durable persistence
Journal for ImmunoTherapy of Cancer | | Liu, F., Keane, J. T., Lewis, H. S., King-Peoples, T. R., June, C. H., Posey, A. D.
Topics: oncology
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