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
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30102 - Immunology
Result continuities
Project
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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
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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
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