A Novel Carcinoembryonic Antigen T-Cell Bispecific Antibody (CEA TCB) for the Treatment of Solid Tumors.

نویسندگان

  • Marina Bacac
  • Tanja Fauti
  • Johannes Sam
  • Sara Colombetti
  • Tina Weinzierl
  • Djamila Ouaret
  • Walter Bodmer
  • Steffi Lehmann
  • Thomas Hofer
  • Ralf J Hosse
  • Ekkehard Moessner
  • Oliver Ast
  • Peter Bruenker
  • Sandra Grau-Richards
  • Teilo Schaller
  • Annette Seidl
  • Christian Gerdes
  • Mario Perro
  • Valeria Nicolini
  • Nathalie Steinhoff
  • Sherri Dudal
  • Sebastian Neumann
  • Thomas von Hirschheydt
  • Christiane Jaeger
  • Jose Saro
  • Vaios Karanikas
  • Christian Klein
  • Pablo Umaña
چکیده

PURPOSE CEA TCB is a novel IgG-based T-cell bispecific (TCB) antibody for the treatment of CEA-expressing solid tumors currently in phase I clinical trials (NCT02324257). Its format incorporates bivalent binding to CEA, a head-to-tail fusion of CEA- and CD3e-binding Fab domains and an engineered Fc region with completely abolished binding to FcγRs and C1q. The study provides novel mechanistic insights into the activity and mode of action of CEA TCB. EXPERIMENTAL DESIGN CEA TCB activity was characterized on 110 cell lines in vitro and in xenograft tumor models in vivo using NOG mice engrafted with human peripheral blood mononuclear cells. RESULTS Simultaneous binding of CEA TCB to tumor and T cells leads to formation of immunologic synapses, T-cell activation, secretion of cytotoxic granules, and tumor cell lysis. CEA TCB activity strongly correlates with CEA expression, with higher potency observed in highly CEA-expressing tumor cells and a threshold of approximately 10,000 CEA-binding sites/cell, which allows distinguishing between high- and low-CEA-expressing tumor and primary epithelial cells, respectively. Genetic factors do not affect CEA TCB activity confirming that CEA expression level is the strongest predictor of CEA TCB activity. In vivo, CEA TCB induces regression of CEA-expressing xenograft tumors with variable amounts of immune cell infiltrate, leads to increased frequency of activated T cells, and converts PD-L1 negative into PD-L1-positive tumors. CONCLUSIONS CEA TCB is a novel generation TCB displaying potent antitumor activity; it is efficacious in poorly infiltrated tumors where it increases T-cell infiltration and generates a highly inflamed tumor microenvironment. Clin Cancer Res; 22(13); 3286-97. ©2016 AACR.

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عنوان ژورنال:
  • Clinical cancer research : an official journal of the American Association for Cancer Research

دوره 22 13  شماره 

صفحات  -

تاریخ انتشار 2016