» Articles » PMID: 39781381

Anti-Mesothelin CAR-NK Cells As a Novel Targeted Therapy Against Cervical Cancer

Abstract

Resistance to the currently available treatment paradigms is one of the main factors that contributes to poor outcomes in patients with advanced cervical cancer. Novel targeted therapy approaches might enhance the patient's treatment outcome and are urgently needed for this malignancy. While chimeric-antigen receptor (CAR)-based adoptive immunotherapy displays a promising treatment strategy for liquid cancers, their use against cervical cancer is largely unexplored. This study used alpharetroviral SIN vectors to equip natural killer (NK) cells with a third-generation CAR (including CD28 and 4-1BB co-stimulatory domains) targeting Mesothelin, which was identified to be highly expressed on primary human cervical cancer tissues and cervical cancer cell lines in this and other studies. Anti-Mesothelin CAR-NK cells demonstrated high cytotoxicity against cervical cancer cells in 2D and 3D culture models, which corresponded to increased degranulation of CAR-NK-92 cells upon exposure to Mesothelin target cells. Mesothelin cervical cancer cells were generated by CRISPR-Cas9-mediated knockout and used to show target antigen specificity of anti-Mesothelin CAR-NK-92 cells and primary NK cells derived from different healthy donors in co-culture experiments. Combination of anti-Mesothelin CAR-NK-92 cells with chemotherapy revealed increased elimination of cancer cells as compared to monotherapy settings. Our findings indicate the promise of anti-Mesothelin CAR-NK cells as a potential treatment option against cervical cancer, as well as other Mesothelin malignancies.

References
1.
Marin D, Li Y, Basar R, Rafei H, Daher M, Dou J . Safety, efficacy and determinants of response of allogeneic CD19-specific CAR-NK cells in CD19 B cell tumors: a phase 1/2 trial. Nat Med. 2024; 30(3):772-784. PMC: 10957466. DOI: 10.1038/s41591-023-02785-8. View

2.
Abruzzese M, Bilotta M, Fionda C, Zingoni A, Soriani A, Vulpis E . Inhibition of bromodomain and extra-terminal (BET) proteins increases NKG2D ligand MICA expression and sensitivity to NK cell-mediated cytotoxicity in multiple myeloma cells: role of cMYC-IRF4-miR-125b interplay. J Hematol Oncol. 2016; 9(1):134. PMC: 5131470. DOI: 10.1186/s13045-016-0362-2. View

3.
Hoffmann D, Schott J, Geis F, Lange L, Muller F, Lenz D . Detailed comparison of retroviral vectors and promoter configurations for stable and high transgene expression in human induced pluripotent stem cells. Gene Ther. 2017; 24(5):298-307. DOI: 10.1038/gt.2017.20. View

4.
Cao B, Liu M, Wang L, Liang B, Feng Y, Chen X . Use of chimeric antigen receptor NK-92 cells to target mesothelin in ovarian cancer. Biochem Biophys Res Commun. 2020; 524(1):96-102. DOI: 10.1016/j.bbrc.2020.01.053. View

5.
De Foucher T, Bendifallah S, Ouldamer L, Bricou A, Lavoue V, Varinot J . Patterns of recurrence and prognosis in locally advanced FIGO stage IB2 to IIB cervical cancer: Retrospective multicentre study from the FRANCOGYN group. Eur J Surg Oncol. 2019; 45(4):659-665. DOI: 10.1016/j.ejso.2018.11.014. View