4.5 Article

γδ T cell activation by bispecific antibodies

Journal

CELLULAR IMMUNOLOGY
Volume 296, Issue 1, Pages 41-49

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.cellimm.2015.04.009

Keywords

Bispecific antibodies; Gammadelta T lymphocytes; Human; Pancreatic ductal adenocarcinoma; Cytotoxicity

Funding

  1. Medical Faculty of Kiel University
  2. DFG Pancreatic Cancer Consortium Kiel [WE 3559/2-1, SE 1831/4-1]
  3. Cluster of Excellence Inflammation-at-Interfaces (EXC 306 Cluster Lab VII) - DFG

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Bispecific antibodies have been successfully introduced into clinical application. gamma delta T cells are of special interest for tumor immunotherapy, due to their recognition of pyrophosphates that are overproduced by many tumor cells resulting in HLA-nonrestricted tumor cell killing. Here we describe in detail a [(Her2)(2) x V gamma 9] tribody construct that targets human V gamma 9 T cells to HER2-expressing tumor cells. The direct comparison with other selective V gamma 9 T cell agonists including phosphoantigens and nitrogen-containing bisphosphonates revealed the superiority of the [(Her2)2 x V gamma 9] tribody in triggering gamma delta T cell-mediated tumor cell killing with negligible induction of gamma delta T cell death. In contrast, phosphoantigens and bisphosphonates are potent inducers of gamma delta T cell proliferation but less efficient enhancers of gamma delta T cell-mediated tumor cell killing. Collectively, our data identify unique properties of a gamma delta T cell-targeting [(Her2)(2) x V gamma 9] tribody which make it an attractive candidate for clinical application in gamma delta T cell-based tumor immunotherapy. (C) 2015 Elsevier Inc. All rights reserved.

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