| Literature DB >> 34072864 |
Hao-Kang Li1, Ching-Wen Hsiao1, Sen-Han Yang1, Hsiu-Ping Yang1, Tai-Sheng Wu1, Chia-Yun Lee1, Yan-Liang Lin1, Janet Pan1, Zih-Fei Cheng1, Yan-Da Lai1, Shih-Chia Hsiao1, Sai-Wen Tang1.
Abstract
Natural killer (NK) cells harbor efficient cytotoxicity against tumor cells without causing life-threatening cytokine release syndrome (CRS) or graft-versus-host disease (GvHD). When compared to chimeric antigen receptor (CAR) technology, Antibody-Cell Conjugation (ACC) technology has been developed to provide an efficient platform to arm immune cells with cancer-targeting antibodies to recognize and attack cancer cells. Recently, we established an endogenous CD16-expressing oNK cell line (oNK) with a favorable expression pattern of NK activation/inhibitory receptors. In this study, we applied ACC platform to conjugate oNK with trastuzumab and an anti-human epidermal growth factor receptor 2 (HER2) antibody. Trastuzumab-conjugated oNK, ACE-oNK-HER2, executed in vitro and in vivo cytotoxicity against HER2-expressing cancer cells and showed enhanced T cell-recruiting capability and secretion of IFNγ. The irradiated and cryopreserved ACE-oNK-HER2, designated as ACE1702, retained superior HER2-specific in vitro and in vivo potency with no tumorigenic potential. In conclusion, this study provides the evidence to support the potential clinical application of ACE1702 as a novel off-the-shelf NK cell therapy against HER2-expressing solid tumors.Entities:
Keywords: ACE1702; HER2; antibody-cell conjugation; cancer cell therapy; natural killer cells; oNK; solid tumor
Year: 2021 PMID: 34072864 DOI: 10.3390/cancers13112724
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639