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Multiparametric flow cytometry analysis of peripheral blood B cell trafficking differences among Epstein-Barr virus infected and uninfected subpopulations

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F20%3A00537110" target="_blank" >RIV/61388971:_____/20:00537110 - isvavai.cz</a>

  • Result on the web

    <a href="https://biomed.papers.upol.cz/artkey/bio-202003-0004_multiparametric-flow-cytometry-analysis-of-peripheral-blood-b-cell-trafficking-differences-among-epstein-barr-v.php" target="_blank" >https://biomed.papers.upol.cz/artkey/bio-202003-0004_multiparametric-flow-cytometry-analysis-of-peripheral-blood-b-cell-trafficking-differences-among-epstein-barr-v.php</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.5507/bp.2019.052" target="_blank" >10.5507/bp.2019.052</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Multiparametric flow cytometry analysis of peripheral blood B cell trafficking differences among Epstein-Barr virus infected and uninfected subpopulations

  • Original language description

    Aims. Epstein-Barr virus (EBV) targets predominantly B cells and these cells could acquire new phenotype characteristics. Here we analyzed whether EBV-infected and -uninfected B cells from healthy subjects differ in proportion of dominant phenotypes, maturation stage, and homing receptors expression.nMethods. EBV-infected and -uninfected cells were identified by flow cytometry using fluorophore-labeled EBV RNA-specific DNA probes combined with fluorophore-labeled antibody to surface lineage markers, integrins, chemokine receptors, and immunoglobulin isotypes, including intracellular ones.nResults. Our results show that the trafficking characteristics of EBERpos B cells are distinct from EBERneg B cells with most dominant differences detected for alpha 4 beta 1 and alpha 4 beta 7 and CCR5 and CCR7. EBV-positive cells are predominantly memory IgM(+) B cells or plasmablasts/plasma cells (PB/PC) positive for IgA or less for IgM. In comparison to uninfected B cells, less EBV-positive B cells express alpha 4 beta 7 and almost no cells express alpha 4 beta 1. EBV-positive B cells contained significantly higher proportion of CCR5(+) and CCR7(+) cells in comparison to EBV-negative cells. In vitro exposure of blood mononuclear cells to pro-inflammatory cytokine IL-6 reduces population of EBV-positive B cell.nConclusion. Although EBV-infected B cells represent only a minor subpopulation, their atypical functions could contribute in predisposed person to development abnormities such as some autoimmune diseases or tumors. Using multi-parameter flow cytometry we characterized differences in migration of EBV-positive and -negative B cells of various maturation stage and isotype of produced antibodies particularly different targeting to mucosal tissues of gastrointestinal and respiratory tracts.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10606 - Microbiology

Result continuities

  • Project

    <a href="/en/project/NV15-33686A" target="_blank" >NV15-33686A: The study of the relation between Epstein-Barr virus infection and development of IgA nephropathy</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    BIOMEDICAL PAPERS-OLOMOUC

  • ISSN

    1804-7521

  • e-ISSN

  • Volume of the periodical

    164

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    CZ - CZECH REPUBLIC

  • Number of pages

    8

  • Pages from-to

    247-254

  • UT code for WoS article

    000595645600004

  • EID of the result in the Scopus database

    2-s2.0-85086109490