CAR memory–like NK cells targeting the membrane proximal domain of mesothelin demonstrate promising activity in ovarian cancer

间皮素 癌症研究 卵巢癌 嵌合抗原受体 生物 免疫疗法 癌症 免疫学 抗原 医学 免疫系统 内科学
作者
Mubin Tarannum,Khanhlinh Dinh,Juliana Vergara,Grace Birch,Yasmin Abdulhamid,Isabel E. Kaplan,Oyku Ay,Andreia Maia,Owen Beaver,Michal Sheffer,Roman M. Shapiro,Alaa Kassim Ali,Han Dong,James Dongjoo Ham,Eden Bobilev,Sydney V. James,Amy B. Cameron,Quang‐Dé Nguyen,Suthakar Ganapathy,Chayapatou Chayawatto
出处
期刊:Science Advances [American Association for the Advancement of Science (AAAS)]
卷期号:10 (28) 被引量:6
标识
DOI:10.1126/sciadv.adn0881
摘要

Epithelial ovarian cancer (EOC) remains one of the most lethal gynecological cancers. Cytokine-induced memory–like (CIML) natural killer (NK) cells have shown promising results in preclinical and early-phase clinical trials. In the current study, CIML NK cells demonstrated superior antitumor responses against a panel of EOC cell lines, increased expression of activation receptors, and up-regulation of genes involved in cell cycle/proliferation and down-regulation of inhibitory/suppressive genes. CIML NK cells transduced with a chimeric antigen receptor (CAR) targeting the membrane-proximal domain of mesothelin (MSLN) further improved the antitumor responses against MSLN-expressing EOC cells and patient-derived xenograft tumor cells. CAR arming of the CIML NK cells subtanstially reduced their dysfunction in patient-derived ascites fluid with transcriptomic changes related to altered metabolism and tonic signaling as potential mechanisms. Lastly, the adoptive transfer of MSLN-CAR CIML NK cells demonstrated remarkable inhibition of tumor growth and prevented metastatic spread in xenograft mice, supporting their potential as an effective therapeutic strategy in EOC.

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