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用于治疗人类癌症的抗癌单克隆抗体的研发与特性分析

Development and Characterization of an Anti-Cancer Monoclonal Antibody for Treatment of Human Carcinomas.

作者信息

Tsang Kwong Yok, Fantini Massimo, Mavroukakis Sharon A, Zaki Anjum, Annunziata Christina M, Arlen Philip M

机构信息

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.

出版信息

Cancers (Basel). 2022 Jun 21;14(13):3037. doi: 10.3390/cancers14133037.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86d0/9264992/8bb8db4b97ee/cancers-14-03037-g001.jpg

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