4.7 Article

Engager T Cells: A New Class of Antigen-specific T Cells That Redirect Bystander T Cells

期刊

MOLECULAR THERAPY
卷 23, 期 1, 页码 171-178

出版社

CELL PRESS
DOI: 10.1038/mt.2014.156

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资金

  1. NIH [P50 CA126752, 1R01CA173750-01]
  2. Leukemia and Lymphoma Society SCOR in Lymphoma
  3. Alex Lemonade Stand Foundation
  4. St. Baldrick's Foundation
  5. Adrienne Helis Malvin Medical Research Foundation
  6. Baylor College of Medicine
  7. Adoptive T-cell Therapy for Lung Cancer Program
  8. NATIONAL CANCER INSTITUTE [R01CA173750, P50CA126752] Funding Source: NIH RePORTER

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Adoptive immunotherapy with antigen-specific T cells has shown promise for the treatment of malignancies. However, infused T cells are unable to redirect resident T cells, limiting potential benefit. While the infusion of bispecific T-cell engagers can redirect resident T cells to tumors, these molecules have a short half-life, and do not self amplify. To overcome these limitations, we generated T cells expressing a secretable T-cell engager specific for CD3 and EphA2, an antigen expressed on a broad range of human tumors (EphA2-ENG T cells). EphA2-ENG T cells were activated and recognized tumor cells in an antigen-dependent manner, redirected bystander T cells to tumor cells, and had potent antitumor activity in glioma and lung cancer severe combined immunodeficiency (SCID) xenograft models associated with a significant survival benefit. This new class of tumor-specific T cells, with the unique ability to redirect bystander T cells, may be a promising alternative to current immunotherapies for cancer.

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