Stimulating T Cells Against Cancer With Agonist Immunostimulatory Monoclonal Antibodies

  • Int Rev Cell Mol Biol. 2019:342:1-25. doi: 10.1016/bs.ircmb.2018.07.003.
Xue Han  1 ,  Matthew D Vesely  2
Affiliations
  • 1. Department of Immunobiology, Yale School of Medicine, New Haven, CT, United States.
  • 2. Department of Dermatology, Yale School of Medicine, New Haven, CT, United States.
Abstract

Elimination of Cancer cells through antitumor immunity has been a long-sought after goal since Sir F. Macfarlane Burnet postulated the theory of immune surveillance against Tumors in the 1950s. Finally, the use of immunotherapeutics against established Cancer is becoming a reality in the past 5years. Most notable are the Monoclonal Antibodies (mAbs) directed against inhibitory T-cell receptors cytotoxic T lymphocyte antigen-4 and programmed death-1. The next generation of mAbs targeting T cells is designed to stimulate costimulatory receptors on T cells. Here we review the recent progress on these immunostimulatory Agonist Antibodies against the costimulatory receptors CD137, GITR, OX40, and CD27.

Keywords
Agonist; Cancer immunotherapy; Immunooncology; Immunostimulatory.