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Comparison of Lymphocyte Populations in Patients With Dobrava or Puumala orthohantavirus Infection

Hemorrhagic fever with renal syndrome (HFRS), caused by Dobrava (DOBV) and Puumala (PUUV) orthohantaviruses, is an endemic disease in Slovenia. DOBV is mainly responsible for a more severe disease, whereas PUUV usually causes a milder form. Therefore, the aim of our study was to determine whether an...

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Autores principales: Resman Rus, Katarina, Kopitar, Andreja Nataša, Korva, Miša, Ihan, Alojz, Petrovec, Miroslav, Avšič-Županc, Tatjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596256/
https://www.ncbi.nlm.nih.gov/pubmed/33178625
http://dx.doi.org/10.3389/fcimb.2020.566149
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author Resman Rus, Katarina
Kopitar, Andreja Nataša
Korva, Miša
Ihan, Alojz
Petrovec, Miroslav
Avšič-Županc, Tatjana
author_facet Resman Rus, Katarina
Kopitar, Andreja Nataša
Korva, Miša
Ihan, Alojz
Petrovec, Miroslav
Avšič-Županc, Tatjana
author_sort Resman Rus, Katarina
collection PubMed
description Hemorrhagic fever with renal syndrome (HFRS), caused by Dobrava (DOBV) and Puumala (PUUV) orthohantaviruses, is an endemic disease in Slovenia. DOBV is mainly responsible for a more severe disease, whereas PUUV usually causes a milder form. Therefore, the aim of our study was to determine whether any differences in lymphocyte population in patients infected with these two viruses exist. Mononuclear cells from peripheral blood (PBMCs) were isolated from DOBV or PUUV infected patients and different lymphocyte subpopulations were analyzed with flow cytometry. Decreased concentrations of lymphocyte subpopulation were observed in DOBV and in PUUV infected patients compared with a healthy control, which was especially evident in DOBV infected patients. The lower values of T cells are likely due to the extravasation of the activated cells from the circulation to the infected tissue. Higher percentage of NK cells were detected in DOBV infected patients in comparison to PUUV infected patients, which could be associated with a more severe HFRS caused by DOBV. PUUV infected patients had a significantly higher concentration of activated T cell subsets, expressing markers CD25, CD69, and HLA-DR in comparison to DOBV infected patients. Higher activation of T cell subsets in PUUV infected patients could be a contributor to a milder HFRS. Further studies are necessary to elucidate the relation between the protective and the harmful role of activated lymphocytes subsets in HFRS pathogenesis.
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spelling pubmed-75962562020-11-10 Comparison of Lymphocyte Populations in Patients With Dobrava or Puumala orthohantavirus Infection Resman Rus, Katarina Kopitar, Andreja Nataša Korva, Miša Ihan, Alojz Petrovec, Miroslav Avšič-Županc, Tatjana Front Cell Infect Microbiol Cellular and Infection Microbiology Hemorrhagic fever with renal syndrome (HFRS), caused by Dobrava (DOBV) and Puumala (PUUV) orthohantaviruses, is an endemic disease in Slovenia. DOBV is mainly responsible for a more severe disease, whereas PUUV usually causes a milder form. Therefore, the aim of our study was to determine whether any differences in lymphocyte population in patients infected with these two viruses exist. Mononuclear cells from peripheral blood (PBMCs) were isolated from DOBV or PUUV infected patients and different lymphocyte subpopulations were analyzed with flow cytometry. Decreased concentrations of lymphocyte subpopulation were observed in DOBV and in PUUV infected patients compared with a healthy control, which was especially evident in DOBV infected patients. The lower values of T cells are likely due to the extravasation of the activated cells from the circulation to the infected tissue. Higher percentage of NK cells were detected in DOBV infected patients in comparison to PUUV infected patients, which could be associated with a more severe HFRS caused by DOBV. PUUV infected patients had a significantly higher concentration of activated T cell subsets, expressing markers CD25, CD69, and HLA-DR in comparison to DOBV infected patients. Higher activation of T cell subsets in PUUV infected patients could be a contributor to a milder HFRS. Further studies are necessary to elucidate the relation between the protective and the harmful role of activated lymphocytes subsets in HFRS pathogenesis. Frontiers Media S.A. 2020-10-16 /pmc/articles/PMC7596256/ /pubmed/33178625 http://dx.doi.org/10.3389/fcimb.2020.566149 Text en Copyright © 2020 Resman Rus, Kopitar, Korva, Ihan, Petrovec and Avšič-Županc. http://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 Cellular and Infection Microbiology
Resman Rus, Katarina
Kopitar, Andreja Nataša
Korva, Miša
Ihan, Alojz
Petrovec, Miroslav
Avšič-Županc, Tatjana
Comparison of Lymphocyte Populations in Patients With Dobrava or Puumala orthohantavirus Infection
title Comparison of Lymphocyte Populations in Patients With Dobrava or Puumala orthohantavirus Infection
title_full Comparison of Lymphocyte Populations in Patients With Dobrava or Puumala orthohantavirus Infection
title_fullStr Comparison of Lymphocyte Populations in Patients With Dobrava or Puumala orthohantavirus Infection
title_full_unstemmed Comparison of Lymphocyte Populations in Patients With Dobrava or Puumala orthohantavirus Infection
title_short Comparison of Lymphocyte Populations in Patients With Dobrava or Puumala orthohantavirus Infection
title_sort comparison of lymphocyte populations in patients with dobrava or puumala orthohantavirus infection
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596256/
https://www.ncbi.nlm.nih.gov/pubmed/33178625
http://dx.doi.org/10.3389/fcimb.2020.566149
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