Spotlight on Natural Killer Cells in Immuno-Oncology

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cellular Immunology".

Deadline for manuscript submissions: 15 February 2026 | Viewed by 1585

Special Issue Editors


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Guest Editor
1. Division of Oral Biology and Medicine, School of Dentistry and Medicine, University of California, Los Angeles, CA 90095, USA
2. The Jonsson Comprehensive Cancer Center, School of Dentistry and Medicine, University of California, Los Angeles, CA 90095, USA
Interests: natural killer cells in cancer immune system
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Guest Editor
Division of Oral Biology and Medicine, The Jane and Jerry Weintraub Center for Reconstructive Biotechnology, Department of Dentistry, University of California Los Angeles (UCLA), Los Angeles, CA 90095, USA
Interests: natural killer cells; oral cancer; pancreatic cancer; cancer immunotherapy; humanized-BLT mice; osteoclasts; cell expansion; T cells; osteonecrosis of jaw; probiotic bacteria; chemotherapy; bisphosphonates; monocytes; dendritic cells; clinical trials; NAC
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Although treatment strategies for cancer have been steadily advancing, we still lack comprehensive and durable treatment modalities to successfully prevent, treat, or cure cancer. In recent years, we have seen approvals of cellular therapies for clinical use; in coming years, we expect to see several others, such as novel natural killer cell (NK), chimeric antigen receptor T-cell (Car-T), tumor infiltrating lymphocyte (TIL), and NK-Car therapies, approved as clinical agents. The ability of NK cells to target cancer stem cells and poorly differentiated tumors that lack adequate levels of MHC class I has afforded primary NK cells a very unique and indispensable role in cancer immunotherapy. It is also known that cancer patients have dysfunctional NK cells in addition to decreased numbers; indeed, inactivation of NK function has been shown to occur at the pre-neoplastic stages of tumorigenesis, making these cells one of the most important immune effectors responsible for the prevention of cancer. However, limitations in the expansion of NK cells to sufficient numbers, the inability to obtain adequate functional NK cells from different cellular sources, and a lack of understanding of the immunobiology of these cells have traditionally hampered progress in the field of NK cell immunotherapy. Therefore, strategies should be designed to allow maintenance of good NK expansion and function in cancer patients since NK cells are known to limit the expansion of Tumor-Associated Macrophages (TAMs), Tregs, and MDSCs in addition to the removal of CSCs/undifferentiated tumors, which are the hallmarks of aggressive tumors. Large numbers of functionally competent NK cells can be combined with other immunotherapeutic strategies such as oncolytic viruses, ADCC inducing antibodies, check point inhibitors, CAR-T, CAR-NK, TIL, and chemotherapeutic and radiotherapeutic strategies for the ultimate goal of tumor eradication.

This collection of comprehensive reviews and original articles should highlight the significant advances made in the field of NK cells, and potential new directions which should help advance the field and bring us to the finish line.

Prof. Dr. Anahid Jewett
Dr. Kawaljit Kaur
Guest Editors

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Keywords

  • natural killer (NK) cells
  • cancer stem cells (CSCs)
  • poorly differentiated tumors
  • differentiation
  • aggressive tumors
  • suppressor cells

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Published Papers (1 paper)

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Research

14 pages, 1588 KiB  
Article
Natural Killer Cell-Secreted IFN-γ and TNF-α Mediated Differentiation in Lung Stem-like Tumors, Leading to the Susceptibility of the Tumors to Chemotherapeutic Drugs
by Kawaljit Kaur, Angie Perez Celis and Anahid Jewett
Cells 2025, 14(2), 90; https://doi.org/10.3390/cells14020090 - 10 Jan 2025
Viewed by 1283
Abstract
We demonstrate that natural killer (NK) cells induce a higher cytotoxicity against lung cancer stem-like cells (hA549) compared to differentiated lung cancer cell lines (H292). The supernatants from split-anergized NK cells (IL-2 and anti-CD16 mAb-treated NK cells) induced differentiation in hA549. Differentiated lung [...] Read more.
We demonstrate that natural killer (NK) cells induce a higher cytotoxicity against lung cancer stem-like cells (hA549) compared to differentiated lung cancer cell lines (H292). The supernatants from split-anergized NK cells (IL-2 and anti-CD16 mAb-treated NK cells) induced differentiation in hA549. Differentiated lung cancer cell line (H292) and NK cells differentiated hA549 expressed reduced NK cell-mediated cytotoxicity but expressed higher sensitivity to chemotherapeutic drugs. This finding validated our previous reports demonstrating that the levels of tumor killing by NK cells and by chemotherapeutic drugs correlate directly and indirectly, respectively, with the stage and levels of tumor differentiation. We also demonstrate the role of IFN-γ and TNF-α in inducing tumor differentiation. NK cells’ supernatants or IFN-γ and TNF-α-induced tumor differentiation was blocked when we used antibodies against IFN-γ and TNF-α. Therefore, IFN-γ and TNF-α released from NK cells play a significant role in differentiating tumors, resulting in increased susceptibility of tumors to chemotherapeutic drugs. We also observed the different effects of MHC-class I antibodies in CSCs vs. differentiated tumors. Treatment with anti-MHC-class I decreased NK cell-mediated cytotoxicity in hA549 tumors, whereas it increased NK cell-mediated cytotoxicity when differentiated tumors were treated with antibodies against MHC-class I. Full article
(This article belongs to the Special Issue Spotlight on Natural Killer Cells in Immuno-Oncology)
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