| Literature DB >> 32042168 |
David G Millar1, Rakesh R Ramjiawan2, Kosuke Kawaguchi2, Nisha Gupta2, Jiang Chen2, Songfa Zhang1, Takashi Nojiri2, William W Ho2, Shuichi Aoki2, Keehoon Jung2, Ivy Chen2, Feng Shi1, James M Heather1, Kohei Shigeta2, Laura T Morton3, Sean Sepulveda1, Li Wan1, Ricky Joseph3, Eleanor Minogue1, Ashok Khatri1, Aditya Bardia4, Leif W Ellisen1, Ryan B Corcoran1, Aaron N Hata1, Sara I Pai5, Rakesh K Jain2, Dai Fukumura2, Dan G Duda2, Mark Cobbold6.
Abstract
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.Entities:
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Year: 2020 PMID: 32042168 PMCID: PMC7456461 DOI: 10.1038/s41587-019-0404-8
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 54.908