Influence of EBV on the Peripheral Blood Memory B Cell Compartment
Author(s) -
Tatyana A. Souza,
B. David Stollar,
John L. Sullivan,
Katherine Luzuriaga,
David A. ThorleyLawson
Publication year - 2007
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.179.5.3153
Subject(s) - biology , compartment (ship) , epstein–barr virus , immunoglobulin d , immunology , peripheral blood , somatic cell , phenotype , immunoglobulin class switching , isotype , b cell , virology , antibody , gene , genetics , virus , oceanography , monoclonal antibody , geology
Peripheral blood memory B cells latently infected with EBV bear somatic mutations and are typically isotype switched consistent with being classical Ag-selected memory B cells. In this work, we performed a comparative analysis of the expressed Ig genes between large sets of EBV-infected and uninfected peripheral blood B cells, isolated from the same infectious mononucleosis patients, to determine whether differences exist that could reveal the influence of EBV on the production and maintenance of these cells. We observed that EBV(+) cells on average accumulated more somatic hypermutations than EBV(-) cells. In addition, they had more replacement mutations and a higher replacement-silent ratio of mutations in their CDRs. We also found that EBV occupies a skewed niche within the memory compartment, due to its exclusion from the CD27(+)IgD(+)IgM(+) subset, but this skewing does not affect the overall structure of the compartment. These results indicate that EBV impacts the mutation and selection process of infected cells but that once they enter memory they cannot be distinguished from uninfected cells by host homeostasis mechanisms.
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