| Literature DB >> 19373228 |
James J Moon1, H Hamlet Chu, Jason Hataye, Antonio J Pagán, Marion Pepper, James B McLachlan, Traci Zell, Marc K Jenkins.
Abstract
The tracking of antigen-specific T cells in vivo is a useful approach for the study of the adaptive immune response. This protocol describes how populations of T cells specific for a given peptide-major histocompatibility complex (pMHC) epitope can be tracked based solely on T-cell receptor (TCR) specificity as opposed to other indirect methods based on function. The methodology involves the adoptive transfer of TCR transgenic T cells with defined epitope specificity into histocompatible mice and the subsequent detection of these cells through the use of congenic or clonotypic markers. Alternatively, endogenous epitope-specific T cells can be tracked directly through the use of pMHC tetramers. Using magnetic bead-based enrichment and advanced multiparameter flow cytometry, populations as small as five epitope-specific T cells can be detected from the peripheral lymphoid organs of a mouse. The adoptive transfer procedure can be completed within 3 h, whereas analysis of epitope-specific cells from mice can be completed within 6 h.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19373228 PMCID: PMC3517879 DOI: 10.1038/nprot.2009.9
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491