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

Author:

Tarannum Mubin1ORCID,Dinh Khanhlinh1ORCID,Vergara Juliana1ORCID,Birch Grace1,Abdulhamid Yasmin Z.1ORCID,Kaplan Isabel E.1ORCID,Ay Oyku1,Maia Andreia1ORCID,Beaver Owen1,Sheffer Michal1ORCID,Shapiro Roman1ORCID,Ali Alaa Kassim1,Dong Han2ORCID,Ham James Dongjoo3ORCID,Bobilev Eden1,James Sydney4,Cameron Amy B.4ORCID,Nguyen Quang-De4ORCID,Ganapathy Suthakar5,Chayawatto Chayapatou5,Koreth John1,Paweletz Cloud P.5,Gokhale Prafulla C.5ORCID,Barbie David A.56,Matulonis Ursula A.7,Soiffer Robert J.1ORCID,Ritz Jerome1ORCID,Porter Rebecca L.7ORCID,Chen Jianzhu3ORCID,Romee Rizwan1ORCID

Affiliation:

1. Division of Transplantation and Cellular Therapies, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

2. Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

3. Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.

4. Lurie Family Imaging Center, Center for Biomedical Imaging in Oncology, Dana Farber Cancer Institute, Boston, MA, USA.

5. Belfer Center for Applied Cancer Science, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

6. Division of Thoracic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

7. Division of Gynecologic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

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