Rational development and characterization of humanized anti–EGFR variant III chimeric antigen receptor T cells for glioblastoma

Laura A. Johnson(University of Pennsylvania), John Scholler(University of Pennsylvania), Takayuki Ohkuri(University of Pittsburgh), Akemi Kosaka(University of Pittsburgh), Prachi Patel(University of Pennsylvania), Shannon E. McGettigan(University of Pennsylvania), Arben Nace(University of Pennsylvania), Tzvete Dentchev(University of Pennsylvania), Pramod Thekkat(Novartis (United States)), Andreas Loew(Novartis (United States)), Alina C. Boesteanu(University of Pennsylvania), Alexandria P. Cogdill(University of Pennsylvania), Taylor Chen(University of Pennsylvania), Joseph A. Fraietta(University of Pennsylvania), Christopher C. Kloss(University of Pennsylvania), Avery D. Posey(University of Pennsylvania), Boris Engels(Novartis (United States)), Reshma Singh(Novartis (United States)), Tucker Ezell(Novartis (United States)), Neeraja Idamakanti(Novartis (United States)), Melissa Ramones(Novartis (United States)), Na Li(Novartis (United States)), Li Zhou(Novartis (United States)), Gabriela Plesa(University of Pennsylvania), John T. Seykora(University of Pennsylvania), Hideho Okada(University of California, San Francisco), Carl H. June(University of Pennsylvania), Jennifer L. Brogdon(Novartis (United States)), Marcela V. Maus(University of Pennsylvania)
Science Translational Medicine
February 18, 2015
Cited by 453

Abstract

Chimeric antigen receptors (CARs) are synthetic molecules designed to redirect T cells to specific antigens. CAR-modified T cells can mediate long-term durable remissions in B cell malignancies, but expanding this platform to solid tumors requires the discovery of surface targets with limited expression in normal tissues. The variant III mutation of the epidermal growth factor receptor (EGFRvIII) results from an in-frame deletion of a portion of the extracellular domain, creating a neoepitope. We chose a vector backbone encoding a second-generation CAR based on efficacy of a murine scFv-based CAR in a xenograft model of glioblastoma. Next, we generated a panel of humanized scFvs and tested their specificity and function as soluble proteins and in the form of CAR-transduced T cells; a low-affinity scFv was selected on the basis of its specificity for EGFRvIII over wild-type EGFR. The lead candidate scFv was tested in vitro for its ability to direct CAR-transduced T cells to specifically lyse, proliferate, and secrete cytokines in response to antigen-bearing targets. We further evaluated the specificity of the lead CAR candidate in vitro against EGFR-expressing keratinocytes and in vivo in a model of mice grafted with normal human skin. EGFRvIII-directed CAR T cells were also able to control tumor growth in xenogeneic subcutaneous and orthotopic models of human EGFRvIII(+) glioblastoma. On the basis of these results, we have designed a phase 1 clinical study of CAR T cells transduced with humanized scFv directed to EGFRvIII in patients with either residual or recurrent glioblastoma (NCT02209376).


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