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一种白细胞介素-15 超激动剂,ALT-803,增强了单克隆抗体 NEO-201 对人癌细胞诱导的抗体依赖的细胞介导的细胞毒性。

An IL-15 Superagonist, ALT-803, Enhances Antibody-Dependent Cell-Mediated Cytotoxicity Elicited by the Monoclonal Antibody NEO-201 Against Human Carcinoma Cells.

机构信息

1 Precision Biologics, Inc., Rockville, Maryland.

2 Altor BioScience Corporation, Miramar, Florida.

出版信息

Cancer Biother Radiopharm. 2019 Apr;34(3):147-159. doi: 10.1089/cbr.2018.2628. Epub 2019 Jan 2.

Abstract

BACKGROUND

A major mechanism of action for therapeutic antibodies is antibody-dependent cell-mediated cytotoxicity (ADCC). ALT-803 is an interleukin-15 superagonist complex that enhances ADCC against human carcinoma cells in vitro and exerts an antitumor activity in murine, rat, and human carcinomas in vivo. The authors investigated the ability of ALT-803 to modulate ADCC mediated by the humanized IgG1 monoclonal antibody (mAb) NEO-201 against human carcinoma cells.

MATERIALS AND METHODS

ALT-803 modulating activity on ADCC mediated by NEO-201 was evaluated on several NEO-201 ligand-expressing human carcinoma cells. Purified human natural killer (NK) cells from multiple healthy donors were treated with ALT-803 before their use as effectors in ADCC assay. Modulation of NK cell phenotype and cytotoxic function by exposure to ALT-803 was evaluated by flow cytometry and gene expression analysis.

RESULTS

ALT-803 significantly enhanced ADCC mediated by NEO-201. ALT-803 also upregulated NK activating receptors, antiapoptotic factors, and factors involved in the NK cytotoxicity, as well as downregulated gene expression of NK inhibiting receptors.

CONCLUSIONS

These findings indicate that ALT-803 can enhance ADCC activity mediated by NEO-201, by modulating NK activation and cytotoxicity, suggesting a possible clinical use of ALT-803 in combination with NEO-201 for the treatment of human carcinomas.

摘要

背景

治疗性抗体的一个主要作用机制是抗体依赖的细胞介导的细胞毒性(ADCC)。ALT-803 是一种白细胞介素-15 超激动剂复合物,可增强体外人癌细胞的 ADCC,并在体内的鼠、大鼠和人癌中发挥抗肿瘤活性。作者研究了 ALT-803 调节针对人癌细胞的人源化 IgG1 单克隆抗体(mAb)NEO-201 介导的 ADCC 的能力。

材料和方法

在几种表达 NEO-201 配体的人癌细胞上评估了 ALT-803 对 NEO-201 介导的 ADCC 的调节作用。从多个健康供体中纯化的人自然杀伤(NK)细胞在用作 ADCC 测定中的效应细胞之前用 ALT-803 处理。通过流式细胞术和基因表达分析评估暴露于 ALT-803 对 NK 细胞表型和细胞毒性功能的调节作用。

结果

ALT-803 显著增强了 NEO-201 介导的 ADCC。ALT-803 还上调了 NK 激活受体、抗凋亡因子和参与 NK 细胞毒性的因子,同时下调了 NK 抑制受体的基因表达。

结论

这些发现表明,ALT-803 可以通过调节 NK 激活和细胞毒性来增强 NEO-201 介导的 ADCC 活性,这表明 ALT-803 与 NEO-201 联合用于治疗人类癌症可能具有临床应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c922/6482908/23ea5ae2b191/fig-1.jpg

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