| Literature DB >> 11339358 |
M G McHeyzer-Williams1, L J McHeyzer-Williams, J Fanelli Panus, G Bikah, R R Pogue-Caley, D J Driver, M D Eisenbraun.
Abstract
Helper T cell-regulated B cell responses constitute a major component of the primary immune response to many pathogens. The subsequent development of antigen-specific immune memory is one critical outcome of this primary adaptive immune response. Antigen-specific immunity develops through a series of intercellular information exchanges organized around cognate T cell receptor-peptide/MHC interactions. Here, we discuss these complex molecularevents andtheircellularconsequences in a serial synapsis model of adaptive immunity. Our laboratory has developed strategies to isolate antigen-specific Th cells and B cells to analyze gene expression and cellular function in single responding lymphocytes directly ex vivo. These studies provide insight into the regulation and cellular organization of antigen-specific immune responses in vivo.Entities:
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Year: 2000 PMID: 11339358 DOI: 10.1385/IR:22:2-3:223
Source DB: PubMed Journal: Immunol Res ISSN: 0257-277X Impact factor: 2.829