| Literature DB >> 26187411 |
Roberto Di Niro1, Seung-Joo Lee2, Jason A Vander Heiden3, Rebecca A Elsner4, Nikita Trivedi4, Jason M Bannock5, Namita T Gupta3, Steven H Kleinstein6, Francois Vigneault7, Tamara J Gilbert7, Eric Meffre5, Stephen J McSorley2, Mark J Shlomchik8.
Abstract
The B cell response to Salmonella typhimurium (STm) occurs massively at extrafollicular sites, without notable germinal centers (GCs). Little is known in terms of its specificity. To expand the knowledge of antigen targets, we screened plasmablast (PB)-derived monoclonal antibodies (mAbs) for Salmonella specificity, using ELISA, flow cytometry, and antigen microarray. Only a small fraction (0.5%-2%) of the response appeared to be Salmonella-specific. Yet, infection of mice with limited B cell receptor (BCR) repertoires impaired the response, suggesting that BCR specificity was important. We showed, using laser microdissection, that somatic hypermutation (SHM) occurred efficiently at extrafollicular sites leading to affinity maturation that in turn led to detectable STm Ag-binding. These results suggest a revised vision of how clonal selection and affinity maturation operate in response to Salmonella. Clonal selection initially is promiscuous, activating cells with virtually undetectable affinity, yet SHM and selection occur during the extrafollicular response yielding higher affinity, detectable antibodies.Entities:
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Year: 2015 PMID: 26187411 PMCID: PMC4523395 DOI: 10.1016/j.immuni.2015.06.013
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745