Massachusetts General Hospital Cancer Center and Department of Medicine, Harvard Medical School, Boston, MA, USA.
Steele Laboratories, Department of Radiation Oncology, Harvard Medical School, Boston, MA, USA.
Nat Biotechnol. 2020 Apr;38(4):420-425. doi: 10.1038/s41587-019-0404-8. Epub 2020 Feb 10.
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.
几种癌症免疫疗法,如免疫检查点阻断和过继性 T 细胞疗法,可增强 T 细胞对肿瘤的活性,但如果没有针对显示的肿瘤抗原的 T 细胞,这些策略就不起作用。在这里,我们概述了一种免疫疗法,其中针对非癌症抗原的内源性 T 细胞被重新定向攻击肿瘤。该方法依赖于使用抗体-肽表位缀合物 (APEC) 将合适的抗原递送到肿瘤表面,由 HLA-I 呈递。为了将巨细胞病毒 (CMV) 特异性 CD8 T 细胞靶向肿瘤,我们使用了含有 CMV 衍生表位的 APEC,通过金属蛋白酶敏感的接头与肿瘤靶向抗体连接。这些 APEC 在体外和小鼠癌症模型中重新定向针对肿瘤细胞的预先存在的 CMV 免疫。在体外,APEC 特异性激活了 CMV 反应性效应 T 细胞,而双特异性 T 细胞衔接器激活了效应 T 细胞和调节性 T 细胞。我们的方法可能为不能接受检查点抑制剂或其他免疫疗法的癌症提供一种有效的替代方法。