Defining antigen-specific plasmablast and memory B cell subsets in human blood after viral infection or vaccination.
Ontology highlight
ABSTRACT: Antigen-specific B cells bifurcate into antibody-secreting cells (ASCs) and memory B cells (MBCs) after infection or vaccination. ASCs (plasmablasts) have been extensively studied in humans, but less is known about B cells that become activated but do not differentiate into plasmablasts. Here we have defined the phenotype and transcriptional program of a subset of antigen-specific B cells, which we have called 'activated B cells' (ABCs), that were distinct from ASCs and were committed to the MBC lineage. We detected ABCs in humans after infection with Ebola virus or influenza virus and also after vaccination. By simultaneously analyzing antigen-specific ASCs and ABCs in human blood after vaccination against influenza virus, we investigated the clonal overlap and extent of somatic hypermuta
SUBMITTER: Ellebedy AH
PROVIDER: S-EPMC5054979 | biostudies-literature | 2016 Oct
REPOSITORIES: biostudies-literature
ACCESS DATA