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 Viroljournal_title
Journal of virologyauthors
Dorner M,Zucol F,Alessi D,Haerle SK,Bossart W,Weber M,Byland R,Bernasconi M,Berger C,Tugizov S,Speck RF,Nadal Ddoi
10.1128/JVI.02675-09subject
Has Abstractpub_date
2010-07-01 00:00:00pages
6667-77issue
13eissn
0022-538Xissn
1098-5514pii
JVI.02675-09journal_volume
84pub_type
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