Tsang Kwong Yok, Fantini Massimo, Mavroukakis Sharon A, Zaki Anjum, Annunziata Christina M, Arlen Philip M
Precision Biologics, Inc., Bethesda, MD 20814, USA.
Women's Malignancy Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Cancers (Basel). 2022 Jun 21;14(13):3037. doi: 10.3390/cancers14133037.
NEO-201 is an IgG1 humanized monoclonal antibody (mAb) that binds to tumor-associated variants of carcinoembryonic antigen-related cell adhesion molecule (CEACAM)-5 and CEACAM-6. NEO-201 reacts to colon, ovarian, pancreatic, non-small cell lung, head and neck, cervical, uterine and breast cancers, but is not reactive against most normal tissues. NEO-201 can kill tumor cells via antibody-dependent cell-mediated cytotoxicity (ADCC) and complement dependent cytotoxicity (CDC) to directly kill tumor cells expressing its target. We explored indirect mechanisms of its action that may enhance immune tumor killing. NEO-201 can block the interaction between CEACAM-5 expressed on tumor cells and CEACAM-1 expressed on natural killer (NK) cells to reverse CEACAM-1-dependent inhibition of NK cytotoxicity. Previous studies have demonstrated safety/tolerability in non-human primates, and in a first in human phase 1 clinical trial at the National Cancer Institute (NCI). In addition, preclinical studies have demonstrated that NEO-201 can bind to human regulatory T (Treg) cells. The specificity of NEO-201 in recognizing suppressive Treg cells provides the basis for combination cancer immunotherapy with checkpoint inhibitors targeting the PD-1/PD-L1 pathway.
NEO-201是一种IgG1人源化单克隆抗体(mAb),可与癌胚抗原相关细胞粘附分子(CEACAM)-5和CEACAM-6的肿瘤相关变体结合。NEO-201可与结肠癌、卵巢癌、胰腺癌、非小细胞肺癌、头颈癌、宫颈癌、子宫癌和乳腺癌发生反应,但对大多数正常组织无反应。NEO-201可通过抗体依赖性细胞介导的细胞毒性(ADCC)和补体依赖性细胞毒性(CDC)杀死肿瘤细胞,以直接杀死表达其靶点的肿瘤细胞。我们探索了其可能增强免疫肿瘤杀伤作用的间接机制。NEO-201可阻断肿瘤细胞上表达的CEACAM-5与自然杀伤(NK)细胞上表达的CEACAM-1之间的相互作用,以逆转CEACAM-1依赖性的NK细胞毒性抑制。先前的研究已证明其在非人灵长类动物以及美国国立癌症研究所(NCI)开展的首例人体1期临床试验中的安全性/耐受性。此外,临床前研究已证明NEO-201可与人调节性T(Treg)细胞结合。NEO-201识别抑制性Treg细胞的特异性为其与靶向PD-1/PD-L1途径的检查点抑制剂联合进行癌症免疫治疗提供了基础。