» Articles » PMID: 35203609

The War Is On: The Immune System Against Glioblastoma-How Can NK Cells Drive This Battle?

Abstract

Natural killer (NK) cells are innate lymphocytes that play an important role in immunosurveillance, acting alongside other immune cells in the response against various types of malignant tumors and the prevention of metastasis. Since their discovery in the 1970s, they have been thoroughly studied for their capacity to kill neoplastic cells without the need for previous sensitization, executing rapid and robust cytotoxic activity, but also helper functions. In agreement with this, NK cells are being exploited in many ways to treat cancer. The broad arsenal of NK-based therapies includes adoptive transfer of in vitro expanded and activated cells, genetically engineered cells to contain chimeric antigen receptors (CAR-NKs), in vivo stimulation of NK cells (by cytokine therapy, checkpoint blockade therapies, etc.), and tumor-specific antibody-guided NK cells, among others. In this article, we review pivotal aspects of NK cells' biology and their contribution to immune responses against tumors, as well as providing a wide perspective on the many antineoplastic strategies using NK cells. Finally, we also discuss those approaches that have the potential to control glioblastoma-a disease that, currently, causes inevitable death, usually in a short time after diagnosis.

Citing Articles

Efficacy Evaluation of "Enhanced" Natural Killers with and Knockouts on Viability and Metabolic Status of 3D Glioblastoma Spheroid Cells in Patients.

Yuzhakova D, Sachkova D, Shirmanova M, Shcheslavskiy V, Mozherov A, Dashinimaev E Sovrem Tekhnologii Med. 2025; 17(1):109-118.

PMID: 40071076 PMC: 11892565. DOI: 10.17691/stm2025.17.1.10.


Cancer Vaccines and Beyond: The Transformative Role of Nanotechnology in Immunotherapy.

Delgado-Almenta V, Blaya-Canovas J, Calahorra J, Lopez-Tejada A, Grinan-Lison C, Granados-Principal S Pharmaceutics. 2025; 17(2).

PMID: 40006583 PMC: 11859086. DOI: 10.3390/pharmaceutics17020216.


IDO1 Inhibitor RY103 Suppresses Trp-GCN2-Mediated Angiogenesis and Counters Immunosuppression in Glioblastoma.

Xing Z, Li X, He Z, Fang X, Liang H, Kuang C Pharmaceutics. 2024; 16(7).

PMID: 39065567 PMC: 11279595. DOI: 10.3390/pharmaceutics16070870.


Systemic and local immunosuppression in glioblastoma and its prognostic significance.

Stepanenko A, Sosnovtseva A, Valikhov M, Chernysheva A, Abramova O, Pavlov K Front Immunol. 2024; 15:1326753.

PMID: 38481999 PMC: 10932993. DOI: 10.3389/fimmu.2024.1326753.


The immunological landscape of peripheral blood in glioblastoma patients and immunological consequences of age and dexamethasone treatment.

Dusoswa S, Verhoeff J, van Asten S, Lubbers J, van den Braber M, Peters S Front Immunol. 2024; 15:1343484.

PMID: 38318180 PMC: 10839779. DOI: 10.3389/fimmu.2024.1343484.


References
1.
Navin I, Lam M, Parihar R . Design and Implementation of NK Cell-Based Immunotherapy to Overcome the Solid Tumor Microenvironment. Cancers (Basel). 2020; 12(12). PMC: 7767468. DOI: 10.3390/cancers12123871. View

2.
Street S, Cretney E, Smyth M . Perforin and interferon-gamma activities independently control tumor initiation, growth, and metastasis. Blood. 2001; 97(1):192-7. DOI: 10.1182/blood.v97.1.192. View

3.
Avril T, Vauleon E, Hamlat A, Saikali S, Etcheverry A, Delmas C . Human glioblastoma stem-like cells are more sensitive to allogeneic NK and T cell-mediated killing compared with serum-cultured glioblastoma cells. Brain Pathol. 2011; 22(2):159-74. PMC: 8029175. DOI: 10.1111/j.1750-3639.2011.00515.x. View

4.
Stoklasek T, Schluns K, Lefrancois L . Combined IL-15/IL-15Ralpha immunotherapy maximizes IL-15 activity in vivo. J Immunol. 2006; 177(9):6072-80. PMC: 2847275. DOI: 10.4049/jimmunol.177.9.6072. View

5.
Grzywacz B, Kataria N, Verneris M . CD56(dim)CD16(+) NK cells downregulate CD16 following target cell induced activation of matrix metalloproteinases. Leukemia. 2007; 21(2):356-9. DOI: 10.1038/sj.leu.2404499. View