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Two vicious circles associated with the aging of the immune system in the development of severe forms of COVID-19
Background: The immune-inflammatory response is the basis of the pathophysiology of SARS-Cov-2 infection. In severe cases of COVID-19 uncontrolled systemic inflammatory response causes multiorgan dysfunction (MODS), as the most common immediate cause of death. Unfavorable outcome of the COVID-19 mos...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537960/ https://www.ncbi.nlm.nih.gov/pubmed/37780864 http://dx.doi.org/10.3389/fragi.2023.1260053 |
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author | Vrbic, Miodrag Milinkovic, Ana |
author_facet | Vrbic, Miodrag Milinkovic, Ana |
author_sort | Vrbic, Miodrag |
collection | PubMed |
description | Background: The immune-inflammatory response is the basis of the pathophysiology of SARS-Cov-2 infection. In severe cases of COVID-19 uncontrolled systemic inflammatory response causes multiorgan dysfunction (MODS), as the most common immediate cause of death. Unfavorable outcome of the COVID-19 most often occurs in elderly patients. The aim of the study was to establish parameters with prognostic significance in severe cases of COVID-19 according to life years, laboratory markers of sepsis and MODS, as well as the number of peripheral CD4(+) and CD8(+)T lymphocytes in 20 consecutively selected critically ill patients. Results: Eleven subjects were male, 9 female, mean age 73.45 ± 11.59, among which the oldest patient was 94 and the youngest 43 years. All the patients met the sepsis and MODS criteria. Increased age and low CD4(+) and CD8(+)T cell counts were identified as independent predictors of death. Only the two youngest patients (43 and 50 years old) survived 28 days, and they are the only ones with a CD4 lymphocyte count above 500 cells/mm(3). Conclusion: Senescence of the immune system is mostly characterized by reduced regenerative capacity of adaptive immunity with diminished ability to respond to new antigens and a manifested proinflammatory phenotype. Additional reduction of protective capacity by further deterioration of T cell quantity and quality due to sepsis itself and mutual interaction of senescent T cells and vascular endothelial cells in the induction of cytokine storm represent two complementary vicious cycles in the development of sepsis-related multiorgan dysfunction. |
format | Online Article Text |
id | pubmed-10537960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105379602023-09-29 Two vicious circles associated with the aging of the immune system in the development of severe forms of COVID-19 Vrbic, Miodrag Milinkovic, Ana Front Aging Aging Background: The immune-inflammatory response is the basis of the pathophysiology of SARS-Cov-2 infection. In severe cases of COVID-19 uncontrolled systemic inflammatory response causes multiorgan dysfunction (MODS), as the most common immediate cause of death. Unfavorable outcome of the COVID-19 most often occurs in elderly patients. The aim of the study was to establish parameters with prognostic significance in severe cases of COVID-19 according to life years, laboratory markers of sepsis and MODS, as well as the number of peripheral CD4(+) and CD8(+)T lymphocytes in 20 consecutively selected critically ill patients. Results: Eleven subjects were male, 9 female, mean age 73.45 ± 11.59, among which the oldest patient was 94 and the youngest 43 years. All the patients met the sepsis and MODS criteria. Increased age and low CD4(+) and CD8(+)T cell counts were identified as independent predictors of death. Only the two youngest patients (43 and 50 years old) survived 28 days, and they are the only ones with a CD4 lymphocyte count above 500 cells/mm(3). Conclusion: Senescence of the immune system is mostly characterized by reduced regenerative capacity of adaptive immunity with diminished ability to respond to new antigens and a manifested proinflammatory phenotype. Additional reduction of protective capacity by further deterioration of T cell quantity and quality due to sepsis itself and mutual interaction of senescent T cells and vascular endothelial cells in the induction of cytokine storm represent two complementary vicious cycles in the development of sepsis-related multiorgan dysfunction. Frontiers Media S.A. 2023-09-14 /pmc/articles/PMC10537960/ /pubmed/37780864 http://dx.doi.org/10.3389/fragi.2023.1260053 Text en Copyright © 2023 Vrbic and Milinkovic. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Aging Vrbic, Miodrag Milinkovic, Ana Two vicious circles associated with the aging of the immune system in the development of severe forms of COVID-19 |
title | Two vicious circles associated with the aging of the immune system in the development of severe forms of COVID-19 |
title_full | Two vicious circles associated with the aging of the immune system in the development of severe forms of COVID-19 |
title_fullStr | Two vicious circles associated with the aging of the immune system in the development of severe forms of COVID-19 |
title_full_unstemmed | Two vicious circles associated with the aging of the immune system in the development of severe forms of COVID-19 |
title_short | Two vicious circles associated with the aging of the immune system in the development of severe forms of COVID-19 |
title_sort | two vicious circles associated with the aging of the immune system in the development of severe forms of covid-19 |
topic | Aging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537960/ https://www.ncbi.nlm.nih.gov/pubmed/37780864 http://dx.doi.org/10.3389/fragi.2023.1260053 |
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