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Myeloid-Derived Suppressor Cells in Cancer and COVID-19 as Associated with Oxidative Stress.

作者信息

Andrés Celia María Curieses, Pérez de la Lastra José Manuel, Juan Celia Andrés, Plou Francisco J, Pérez-Lebeña Eduardo

机构信息

Hospital Clínico Universitario of Valladolid, Avenida de Ramón y Cajal 3, 47003 Valladolid, Spain.

Cinquima Institute and Department of Organic Chemistry, Faculty of Sciences, Valladolid University, Paseo de Belén 7, 47011 Valladolid, Spain.

出版信息

Vaccines (Basel). 2023 Jan 19;11(2):218. doi: 10.3390/vaccines11020218.


DOI:10.3390/vaccines11020218
PMID:36851096
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9966263/
Abstract

Myeloid-derived suppressor cells MDSCs are a heterogeneous population of cells that expand beyond their physiological regulation during pathologies such as cancer, inflammation, bacterial, and viral infections. Their key feature is their remarkable ability to suppress T cell and natural killer NK cell responses. Certain risk factors for severe COVID-19 disease, such as obesity and diabetes, are associated with oxidative stress. The resulting inflammation and oxidative stress can negatively impact the host. Similarly, cancer cells exhibit a sustained increase in intrinsic ROS generation that maintains the oncogenic phenotype and drives tumor progression. By disrupting endoplasmic reticulum calcium channels, intracellular ROS accumulation can disrupt protein folding and ultimately lead to proteostasis failure. In cancer and COVID-19, MDSCs consist of the same two subtypes (PMN-MSDC and M-MDSC). While the main role of polymorphonuclear MDSCs is to dampen the response of T cells and NK killer cells, they also produce reactive oxygen species ROS and reactive nitrogen species RNS. We here review the origin of MDSCs, their expansion mechanisms, and their suppressive functions in the context of cancer and COVID-19 associated with the presence of superoxide anion O and reactive oxygen species ROS.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58a7/9966263/2f1fd34b04f1/vaccines-11-00218-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58a7/9966263/4bedbfbb362c/vaccines-11-00218-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58a7/9966263/0bb8dfa2d47e/vaccines-11-00218-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58a7/9966263/550b198fc5a6/vaccines-11-00218-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58a7/9966263/2f1fd34b04f1/vaccines-11-00218-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58a7/9966263/4bedbfbb362c/vaccines-11-00218-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58a7/9966263/0bb8dfa2d47e/vaccines-11-00218-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58a7/9966263/550b198fc5a6/vaccines-11-00218-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58a7/9966263/2f1fd34b04f1/vaccines-11-00218-g004.jpg

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[1]
Myeloid-Derived Suppressor Cells in Cancer and COVID-19 as Associated with Oxidative Stress.

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[10]
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[1]
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[2]
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[3]
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[4]
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本文引用的文献

[1]
Cancer chemotherapy and beyond: Current status, drug candidates, associated risks and progress in targeted therapeutics.

Genes Dis. 2022-3-18

[2]
The Role of Reactive Species on Innate Immunity.

Vaccines (Basel). 2022-10-17

[3]
Hypochlorous Acid Chemistry in Mammalian Cells-Influence on Infection and Role in Various Pathologies.

Int J Mol Sci. 2022-9-14

[4]
High generation of reactive oxygen species from neutrophils in patients with severe COVID-19.

Sci Rep. 2022-6-21

[5]
ROS and Endoplasmic Reticulum Stress in Pulmonary Disease.

Front Pharmacol. 2022-4-26

[6]
Neutrophil-to-Lymphocyte Ratio as a Predictor of Disease Severity and Mortality in Coronavirus Disease 2019: Prospective Study From Central India.

Cureus. 2022-3-31

[7]
Tumor-infiltrating T-regulatory cells adapt to altered metabolism to promote tumor-immune escape.

Curr Res Immunol. 2021-8-28

[8]
Implication of COVID-19 on Erythrocytes Functionality: Red Blood Cell Biochemical Implications and Morpho-Functional Aspects.

Int J Mol Sci. 2022-2-16

[9]
Immune mechanisms in cancer patients that lead to poor outcomes of SARS-CoV-2 infection.

Transl Res. 2022-3

[10]
The impact of DAMP-mediated inflammation in severe COVID-19 and related disorders.

Biochem Pharmacol. 2022-1

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