J 2021

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

TICHA, Olga, Peter SLANINA, Lukas MOOS, Julie ŠTÍCHOVÁ, Marcela VLKOVÁ et. al.

Základní údaje

Originální název

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

Autoři

TICHA, Olga (203 Česká republika), Peter SLANINA (703 Slovensko, domácí), Lukas MOOS, Julie ŠTÍCHOVÁ (203 Česká republika, domácí), Marcela VLKOVÁ (203 Česká republika, domácí) a Isabelle BEKEREDJIAN-DING (garant)

Vydání

EUROPEAN JOURNAL OF IMMUNOLOGY, HOBOKEN, WILEY, 2021, 0014-2980

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30102 Immunology

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 6.688

Kód RIV

RIV/00216224:14110/21:00121608

Organizační jednotka

Lékařská fakulta

UT WoS

000626550800001

Klíčová slova anglicky

B cells; Breg; IL‐ 10; TLR9; TNFR2

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 7. 12. 2021 13:44, Mgr. Tereza Miškechová

Anotace

V originále

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.