beta1 integrin expression increases susceptibility of memory B cells to Epstein-Barr virus infection.

Abstract:

:Epstein-Barr virus (EBV) uses nasal mucosa-associated lymphoid tissue (NALT) as a portal of entry to establish life-long persistence in memory B cells. We previously showed that naïve and memory B cells from NALT are equally susceptible to EBV infection. Here we show that memory B cells from NALT are significantly more susceptible to EBV infection than those from remote lymphatic organs. We identify beta(1) integrin, which is expressed the most by naïve B cells of distinct lymphoid origin and by memory B cells from NALT, as a mediator of increased susceptibility to infection by EBV. Furthermore, we show that BMRF-2-beta(1) integrin interaction and the downstream signal transduction pathway are critical for postbinding events. An increase of beta(1) integrin expression in peripheral blood memory B cells provoked by CD40 stimulation plus B-cell receptor cross-linking increased the susceptibility of non-NALT memory B cells to EBV infection. Thus, EBV seems to utilize the increased activation status of memory B cells residing in the NALT to establish and ensure persistence.

journal_name

J Virol

journal_title

Journal of virology

authors

Dorner M,Zucol F,Alessi D,Haerle SK,Bossart W,Weber M,Byland R,Bernasconi M,Berger C,Tugizov S,Speck RF,Nadal D

doi

10.1128/JVI.02675-09

subject

Has Abstract

pub_date

2010-07-01 00:00:00

pages

6667-77

issue

13

eissn

0022-538X

issn

1098-5514

pii

JVI.02675-09

journal_volume

84

pub_type

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