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Antibody-mediated delivery of viral epitopes to tumors harnesses CMV-specific T cells for cancer therapy.

David G MillarRakesh R RamjiawanKosuke KawaguchiNisha GuptaJiang ChenSongfa ZhangTakashi NojiriWilliam W HoShuichi AokiKeehoon JungIvy ChenFeng ShiJames M HeatherKohei ShigetaLaura T MortonSean SepulvedaLi WanRicky JosephEleanor MinogueAshok KhatriAditya BardiaLeif W EllisenRyan B CorcoranAaron N HataSara I PaiRakesh K JainDai FukumuraDan G DudaMark Cobbold
Published in: Nature biotechnology (2020)
Several cancer immunotherapy approaches, such as immune checkpoint blockade and adoptive T-cell therapy, boost T-cell activity against the tumor, but these strategies are not effective in the absence of T cells specific for displayed tumor antigens. Here we outline an immunotherapy in which endogenous T cells specific for a noncancer antigen are retargeted to attack tumors. The approach relies on the use of antibody-peptide epitope conjugates (APECs) to deliver suitable antigens to the tumor surface for presention by HLA-I. To retarget cytomegalovirus (CMV)-specific CD8+ T cells against tumors, we used APECs containing CMV-derived epitopes conjugated to tumor-targeting antibodies via metalloprotease-sensitive linkers. These APECs redirect pre-existing CMV immunity against tumor cells in vitro and in mouse cancer models. In vitro, APECs activated specifically CMV-reactive effector T cells whereas a bispecific T-cell engager activated both effector and regulatory T cells. Our approach may provide an effective alternative in cancers that are not amenable to checkpoint inhibitors or other immunotherapies.
Keyphrases
  • regulatory t cells
  • cell therapy
  • cancer therapy
  • dendritic cells
  • stem cells
  • drug delivery
  • sars cov
  • epstein barr virus
  • immune response
  • bone marrow
  • cell proliferation
  • type iii