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TREC/KREC Levels and T and B Lymphocyte Subpopulations in COVID-19 Patients at Different Stages of the Disease

Background: T and B cell-mediated immunity can be assessed using T cell receptor excision circle (TREC) and Kappa-deleting recombination excision circle (KREC) analysis, respectively, and successful implementation of this method requires evaluation of the correlation between the TREC frequencies and...

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Autores principales: Savchenko, Andrei A., Tikhonova, Elena, Kudryavtsev, Igor, Kudlay, Dmitry, Korsunsky, Ilya, Beleniuk, Vasily, Borisov, Alexandr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954181/
https://www.ncbi.nlm.nih.gov/pubmed/35337053
http://dx.doi.org/10.3390/v14030646
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author Savchenko, Andrei A.
Tikhonova, Elena
Kudryavtsev, Igor
Kudlay, Dmitry
Korsunsky, Ilya
Beleniuk, Vasily
Borisov, Alexandr
author_facet Savchenko, Andrei A.
Tikhonova, Elena
Kudryavtsev, Igor
Kudlay, Dmitry
Korsunsky, Ilya
Beleniuk, Vasily
Borisov, Alexandr
author_sort Savchenko, Andrei A.
collection PubMed
description Background: T and B cell-mediated immunity can be assessed using T cell receptor excision circle (TREC) and Kappa-deleting recombination excision circle (KREC) analysis, respectively, and successful implementation of this method requires evaluation of the correlation between the TREC frequencies and T cell subsets as well as KREC levels and B lymphocyte subsets. The aim of the present study was to evaluate the correlation between the TREC/KREC concentrations and T/B lymphocyte subsets at different stages of COVID-19. Methods: We examined 33 patients in the acute stage of COVID-19 (including 8 patients with poor outcomes) and 33 COVID-19 survivors. TREC/KREC concentrations were measured using quantitative real-time PCR. T/B lymphocyte subsets were determined using flow cytometry. Results: Blood TREC and KREC levels were found to be significantly lower in the acute stage of COVID-19 compared to control values. Moreover, a zero blood TREC level was a predictor of a poor disease outcome. Reductions in CD3(+)CD4(+)CD45RO(−)CD62L(−) and CD3(+)CD8(+)CD45RO(−)CD62L(−) T cell counts (as well as in the main fractions of B1 and B2 B cells) indicated a favorable outcome in COVID-19 patients in the acute stage of the disease. Decreased CD3(+)CD4(+)CD45RO(−)CD62L(+) and CD3(+)CD8(+)CD45RO(−)CD62L(+) T cell frequencies and increased CD3(+)CD8(+)CD45RO(−)CD62L(−) cell counts were found to indicate a poor outcome in patients with acute COVID-19. These patients were also found to have increased B1 cell counts while demonstrating no changes in B2 cell counts. The levels of effector T cell subsets an naïve B cells were normal in COVID-19 survivors. The most pronounced correlations between TREC/KREC levels and T/B cell subsets counts were observed in COVID-19 survivors: there were positive correlations with naïve T and B lymphocytes and negative correlations with central and effector memory T cell subsets. Conclusions: The assessment of correlations between TREC and T cell subsets as well as KREC levels and B cell subset counts in patients with acute COVID-19 and COVID-19 survivors has shown that blood concentrations of TREC and KREC are sensitive indicators of the stage of antigen-independent differentiation of adaptive immunity cells. The results of the TREC and KREC analysis correlated with the stages of COVID-19 and differed depending on the outcome of COVID-19.
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spelling pubmed-89541812022-03-26 TREC/KREC Levels and T and B Lymphocyte Subpopulations in COVID-19 Patients at Different Stages of the Disease Savchenko, Andrei A. Tikhonova, Elena Kudryavtsev, Igor Kudlay, Dmitry Korsunsky, Ilya Beleniuk, Vasily Borisov, Alexandr Viruses Article Background: T and B cell-mediated immunity can be assessed using T cell receptor excision circle (TREC) and Kappa-deleting recombination excision circle (KREC) analysis, respectively, and successful implementation of this method requires evaluation of the correlation between the TREC frequencies and T cell subsets as well as KREC levels and B lymphocyte subsets. The aim of the present study was to evaluate the correlation between the TREC/KREC concentrations and T/B lymphocyte subsets at different stages of COVID-19. Methods: We examined 33 patients in the acute stage of COVID-19 (including 8 patients with poor outcomes) and 33 COVID-19 survivors. TREC/KREC concentrations were measured using quantitative real-time PCR. T/B lymphocyte subsets were determined using flow cytometry. Results: Blood TREC and KREC levels were found to be significantly lower in the acute stage of COVID-19 compared to control values. Moreover, a zero blood TREC level was a predictor of a poor disease outcome. Reductions in CD3(+)CD4(+)CD45RO(−)CD62L(−) and CD3(+)CD8(+)CD45RO(−)CD62L(−) T cell counts (as well as in the main fractions of B1 and B2 B cells) indicated a favorable outcome in COVID-19 patients in the acute stage of the disease. Decreased CD3(+)CD4(+)CD45RO(−)CD62L(+) and CD3(+)CD8(+)CD45RO(−)CD62L(+) T cell frequencies and increased CD3(+)CD8(+)CD45RO(−)CD62L(−) cell counts were found to indicate a poor outcome in patients with acute COVID-19. These patients were also found to have increased B1 cell counts while demonstrating no changes in B2 cell counts. The levels of effector T cell subsets an naïve B cells were normal in COVID-19 survivors. The most pronounced correlations between TREC/KREC levels and T/B cell subsets counts were observed in COVID-19 survivors: there were positive correlations with naïve T and B lymphocytes and negative correlations with central and effector memory T cell subsets. Conclusions: The assessment of correlations between TREC and T cell subsets as well as KREC levels and B cell subset counts in patients with acute COVID-19 and COVID-19 survivors has shown that blood concentrations of TREC and KREC are sensitive indicators of the stage of antigen-independent differentiation of adaptive immunity cells. The results of the TREC and KREC analysis correlated with the stages of COVID-19 and differed depending on the outcome of COVID-19. MDPI 2022-03-21 /pmc/articles/PMC8954181/ /pubmed/35337053 http://dx.doi.org/10.3390/v14030646 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Savchenko, Andrei A.
Tikhonova, Elena
Kudryavtsev, Igor
Kudlay, Dmitry
Korsunsky, Ilya
Beleniuk, Vasily
Borisov, Alexandr
TREC/KREC Levels and T and B Lymphocyte Subpopulations in COVID-19 Patients at Different Stages of the Disease
title TREC/KREC Levels and T and B Lymphocyte Subpopulations in COVID-19 Patients at Different Stages of the Disease
title_full TREC/KREC Levels and T and B Lymphocyte Subpopulations in COVID-19 Patients at Different Stages of the Disease
title_fullStr TREC/KREC Levels and T and B Lymphocyte Subpopulations in COVID-19 Patients at Different Stages of the Disease
title_full_unstemmed TREC/KREC Levels and T and B Lymphocyte Subpopulations in COVID-19 Patients at Different Stages of the Disease
title_short TREC/KREC Levels and T and B Lymphocyte Subpopulations in COVID-19 Patients at Different Stages of the Disease
title_sort trec/krec levels and t and b lymphocyte subpopulations in covid-19 patients at different stages of the disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954181/
https://www.ncbi.nlm.nih.gov/pubmed/35337053
http://dx.doi.org/10.3390/v14030646
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