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TNFR2 expression is a hallmark of human memory B cells with suppressive function

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F21%3A00074699" target="_blank" >RIV/00159816:_____/21:00074699 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14110/21:00121608

  • Result on the web

    <a href="https://onlinelibrary.wiley.com/doi/10.1002/eji.202048988" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1002/eji.202048988</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/eji.202048988" target="_blank" >10.1002/eji.202048988</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    TNFR2 expression is a hallmark of human memory B cells with suppressive function

  • Original language description

    Tumor Necrosis Factor Receptor 2 (TNFR2) expression is increasingly being linked to tolerogenic immune reactions and cells with suppressor function including a subset of T-regulatory cells. B-regulatory cells play an important role in control of T-cell responses and inflammation. Recently, we described TNFR2 as a marker for IL-10-producing B cells, a hallmark of this cell subset. Here, we demonstrate that proliferation of T cells is reduced in the presence of TNFR2 positive human memory B cells generated with TLR9 ligand, while TNFR2- and TNFR2+CD27- B cells display costimulatory activity. Our data further reveal that IL-10 secretion is characteristic of IgM+ naive and memory B cells but suppressive activity is not restricted to IL-10: (i) the inhibitory effect of TNFR2+ switched memory B cells was comparable to that exerted by TNFR2+ IgM+ memory B cells although IL-10 secretion levels in the cocultures were lower; (ii) supernatants from TNFR2+ memory B cells failed to suppress T-cell proliferation. Based on our findings, we propose that formation of Breg is a specific characteristic of human memory B cells undergoing terminal differentiation. Our data further corroborate that TNFR2 represents a viable marker for identification of memory B cells with regulatory function.

  • 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

    30102 - Immunology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    EUROPEAN JOURNAL OF IMMUNOLOGY

  • ISSN

    0014-2980

  • e-ISSN

  • Volume of the periodical

    51

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    1195-1205

  • UT code for WoS article

    000626550800001

  • EID of the result in the Scopus database