Department of Chemistry, Lehigh University, Bethlehem, Pennsylvania 18015, United States.
Department of Chemistry, University of Virginia, Charlottesville, Virginia 22904, United States.
J Med Chem. 2020 Apr 9;63(7):3713-3722. doi: 10.1021/acs.jmedchem.0c00016. Epub 2020 Mar 30.
A growing class of immunotherapeutics work by redirecting components of the immune system to recognize markers on the surface of cancer cells. However, such modalities will remain confined to a relatively small subgroup of patients because of the lack of universal targetable tumor biomarkers among all patients. Here, we designed a unique class of agents that exploit the inherent acidity of solid tumors to selectively graft cancer cells with immuno-engager epitopes. Our targeting approach is based on pHLIP, a unique peptide that selectively targets tumors by anchoring to cancer cell surfaces in a pH-dependent manner. We established that pHLIP-antigen conjugates trigger the recruitment of antibodies to the surface of cancer cells and induce cytotoxicity by peripheral blood mononuclear and engineered NK cells. These results indicate that these agents have the potential to be applicable to treating a wide range of solid tumors and to circumvent problems associated with narrow windows of selectivity.
越来越多的免疫疗法通过重新定向免疫系统的成分来识别癌细胞表面的标志物。然而,由于缺乏所有患者都可靶向的通用肿瘤生物标志物,此类方法仍将局限于相对较小的患者亚组。在这里,我们设计了一类独特的药物,利用实体瘤固有的酸度,选择性地将免疫效应分子表位嫁接到癌细胞上。我们的靶向方法基于 pHLIP,这是一种独特的肽,通过以 pH 依赖性的方式锚定在癌细胞表面,选择性地靶向肿瘤。我们证实 pHLIP-抗原缀合物可触发抗体募集到癌细胞表面,并通过外周血单核细胞和工程 NK 细胞诱导细胞毒性。这些结果表明,这些药物有可能适用于治疗广泛的实体瘤,并避免与选择性窗口狭窄相关的问题。