The BiTE (bispecific T-cell engager) platform: Development and future potential of a targeted immuno-oncology therapy across tumor types

Cancer. 2020 Jul 15;126(14):3192-3201. doi: 10.1002/cncr.32909. Epub 2020 May 13.

Abstract

Immuno-oncology therapies engage the immune system to treat cancer. BiTE (bispecific T-cell engager) technology is a targeted immuno-oncology platform that connects patients' own T cells to malignant cells. The modular nature of BiTE technology facilitates the generation of molecules against tumor-specific antigens, allowing off-the-shelf immuno-oncotherapy. Blinatumomab was the first approved canonical BiTE molecule and targets CD19 surface antigens on B cells, making blinatumomab largely independent of genetic alterations or intracellular escape mechanisms. Additional BiTE molecules in development target other hematologic malignancies (eg, multiple myeloma, acute myeloid leukemia, and B-cell non-Hodgkin lymphoma) and solid tumors (eg, prostate cancer, glioblastoma, gastric cancer, and small-cell lung cancer). BiTE molecules with an extended half-life relative to the canonical BiTE molecules are also being developed. Advances in immuno-oncology made with BiTE technology could substantially improve the treatment of hematologic and solid tumors and offer enhanced activity in combination with other treatments.

Keywords: B cell; T cell; blinatumomab; hematologic malignancies; tumor-specific antigen.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adolescent
  • Adult
  • Antibodies, Bispecific / therapeutic use*
  • Antigens, CD19 / immunology
  • Antigens, Neoplasm / immunology
  • Antineoplastic Agents / therapeutic use*
  • B-Lymphocytes / immunology
  • Child
  • Child, Preschool
  • Female
  • Hematologic Neoplasms / therapy*
  • Humans
  • Immunotherapy, Adoptive / methods*
  • Male
  • Middle Aged
  • Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / therapy*
  • Receptors, Chimeric Antigen / immunology*
  • T-Lymphocytes / immunology*
  • Treatment Outcome
  • Young Adult

Substances

  • Antibodies, Bispecific
  • Antigens, CD19
  • Antigens, Neoplasm
  • Antineoplastic Agents
  • CD19 molecule, human
  • Receptors, Chimeric Antigen
  • blinatumomab

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