» Articles » PMID: 33995422

Natural Killer Cells: The Linchpin for Successful Cancer Immunotherapy

Overview
Journal Front Immunol
Date 2021 May 17
PMID 33995422
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Cancer immunotherapy is a highly successful and rapidly evolving treatment modality that works by augmenting the body's own immune system. While various immune stimulation strategies such as PD-1/PD-L1 or CTLA-4 checkpoint blockade result in robust responses, even in patients with advanced cancers, the overall response rate is low. While immune checkpoint inhibitors are known to enhance cytotoxic T cells' antitumor response, current evidence suggests that immune responses independent of cytotoxic T cells, such as Natural Killer (NK) cells, play crucial role in the efficacy of immunotherapeutic interventions. NK cells hold a distinct role in potentiating the innate immune response and activating the adaptive immune system. This review highlights the importance of the early actions of the NK cell response and the pivotal role NK cells hold in priming the immune system and setting the stage for successful response to cancer immunotherapy. Yet, in many patients the NK cell compartment is compromised thus lowering the chances of successful outcomes of many immunotherapies. An overview of mechanisms that can drive NK cell dysfunction and hinder immunotherapy success is provided. Rather than relying on the likely dysfunctional endogenous NK cells to work with immunotherapies, adoptive allogeneic NK cell therapies provide a viable solution to increase response to immunotherapies. This review highlights the advances made in development of NK cell therapeutics for clinical application with evidence supporting their combinatorial application with other immune-oncology approaches to improve outcomes of immunotherapies.

Citing Articles

Synthetic short mRNA prevents metastasis via innate-adaptive immunity.

Hayashi H, Seki S, Tomita T, Kato M, Ashihara N, Chano T Nat Commun. 2025; 16(1):1925.

PMID: 40000682 PMC: 11862117. DOI: 10.1038/s41467-025-57123-y.


Comprehensive analysis of LRRC42 as a potential biomarker and key cellular processes in cancer development.

Huang R, Yao J, Liu L, Li H, Huang B Sci Rep. 2025; 15(1):5169.

PMID: 39939664 PMC: 11821809. DOI: 10.1038/s41598-025-88467-6.


Establishment and bioinformatics analysis of a four-miRNA prognostic signature for pleural mesothelioma.

Yang X, Lin Y, Dong B, Li B, Liu R, Wang X J Cancer. 2024; 15(20):6505-6520.

PMID: 39668817 PMC: 11632982. DOI: 10.7150/jca.101914.


Advancements in Cancer Therapy: Mycoviruses and Their Oncolytic Potential.

Kamala K, Ganapathy D, Sivaperumal P Cell Biochem Biophys. 2024; .

PMID: 39535660 DOI: 10.1007/s12013-024-01608-y.


Parainfluenza Virus 5 V Protein Blocks Interferon Gamma-Mediated Upregulation of NK Cell Inhibitory Ligands and Improves NK Cell Killing of Neuroblastoma Cells.

Shiffer E, Oyer J, Copik A, Parks G Viruses. 2024; 16(8).

PMID: 39205244 PMC: 11359056. DOI: 10.3390/v16081270.


References
1.
Spranger S, Dai D, Horton B, Gajewski T . Tumor-Residing Batf3 Dendritic Cells Are Required for Effector T Cell Trafficking and Adoptive T Cell Therapy. Cancer Cell. 2017; 31(5):711-723.e4. PMC: 5650691. DOI: 10.1016/j.ccell.2017.04.003. View

2.
Mariathasan S, Turley S, Nickles D, Castiglioni A, Yuen K, Wang Y . TGFβ attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells. Nature. 2018; 554(7693):544-548. PMC: 6028240. DOI: 10.1038/nature25501. View

3.
Gooding R, Riches P, Dadian G, Moore J, Gore M . Increased soluble interleukin-2 receptor concentration in plasma predicts a decreased cellular response to IL-2. Br J Cancer. 1995; 72(2):452-5. PMC: 2033994. DOI: 10.1038/bjc.1995.354. View

4.
Baggio L, Laureano A, da Rocha Silla L, Lee D . Natural killer cell adoptive immunotherapy: Coming of age. Clin Immunol. 2016; 177:3-11. DOI: 10.1016/j.clim.2016.02.003. View

5.
Imai K, Matsuyama S, Miyake S, Suga K, Nakachi K . Natural cytotoxic activity of peripheral-blood lymphocytes and cancer incidence: an 11-year follow-up study of a general population. Lancet. 2000; 356(9244):1795-9. DOI: 10.1016/S0140-6736(00)03231-1. View