Elsevier

Human Immunology

Volume 83, Issue 1, January 2022, Pages 86-98
Human Immunology

Review
Exhausted NK cells and cytokine storms in COVID-19: Whether NK cell therapy could be a therapeutic choice

https://doi.org/10.1016/j.humimm.2021.09.004Get rights and content

Highlights

  • SARS-CoV-2 subtly disrupts the equations of immune responses in COVID-19 patients.

  • The virus activates infected macrophages and CD4+ T cells to induce cytokine storm.

  • Cytokine storm and direct interaction of viruses inhibit NK cell cytolytic effect.

  • Exhausted NK cell fails to lyse infected cells to avoid their unleashed cytokine release.

  • Adoptive transfer of cytolytic NK cell may reduce cytokine storm while decreasing viral load.

Abstract

The global outbreak of coronavirus-2019 (COVID-19) still claims more lives daily around the world due to the lack of a definitive treatment and the rapid tendency of virus to mutate, which even jeopardizes vaccination efficacy. At the forefront battle against SARS-CoV-2, an effective innate response to the infection has a pivotal role in the initial control and treatment of disease. However, SARS-CoV-2 subtly interrupts the equations of immune responses, disrupting the cytolytic antiviral effects of NK cells, while seriously activating infected macrophages and other immune cells to induce an unleashed “cytokine storm”, a dangerous and uncontrollable inflammatory response causing life-threatening symptoms in patients. Notably, the NK cell exhaustion with ineffective cytolytic function against the sources of exaggerated cytokine release, acts as an Achilles’ heel which exacerbates the severity of COVID-19. Given this, approaches that improve NK cell cytotoxicity may benefit treatment protocols. As a suggestion, adoptive transfer of NK or CAR-NK cells with proper cytotolytic potentials and the lowest capacity of cytokine-release (for example CD56dim NK cells brightly express activating receptors), to severe COVID-19 patients may provide an effective cure especially in cases suffering from cytokine storms. More intriguingly, the ongoing evidence for persistent clonal expansion of NK memory cells characterized by an activating phenotype in response to viral infections, can benefit the future studies on vaccine development and adoptive NK cell therapy in COVID-19. Whether vaccinated volunteers or recovered patients can also be considered as suitable candidates for cell donation could be the subject of future research.

Keywords

Adoptive cell therapy
CD8+ T cell
Coronavirus disease 2019 (COVID-19)
Cytokine storm
Innate immune response
Memory cells
NK cell
SARS-CoV-2
Vaccine

Abbreviations

ACE
Angiotensin converting enzyme
ADCC
Antibody-dependent cellular cytotoxicity
ARDS
Acute respiratory distress syndrome
CAR-NK
Chimeric antigen receptor-NK
COVID-19
Corona virus disease 2019
CRS
cytokine release syndrome
DCs
Dendritic cells
DNAM
DNAX Accessory Molecule
G-CSF
Granulocyte-colony stimulating factor
GM-CSF
Granulocyte macrophage colony-stimulating factor
HLA
Human leukocyte antigen
ICAM
Intercellular Adhesion Molecule
ICU
Intensive care unit
IFN
Interferon
IL
Interleukin
IP-10
IFN-γ-inducible protein 10
KIRs
Killer immunoglobulin-like receptors
MCP
Monocyte chemoattractant protein
MDA
Melanoma differentiation-associated protein
MERS
Middle East respiratory syndrome
MHC
Major histocompatibility
MIG
Monokine induced by gamma interferon
MIP
Macrophage inflammatory protein
NCRs
Natural cytotoxicity receptors
NK
Natural killer
NKD
NK cell deficiency
PAMPs
Pathogen associated molecular patterns
PBMCs
Peripheral blood mononuclear cells
PRRs
Pattern recognition receptors
RANTES
Regulated upon Activation, Normal T Cell Expressed and Presumably Secreted
RIG
Retinoic acid-inducible gene
SARS-CoV
Severe acute respiratory syndrome-coronavirus
TGF
Transforming growth factor
TLR
Toll-like receptor
TNF
Tumor necrosis factor

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