Journal of immunological methods · 2011
Use of replication restricted recombinant vesicular stomatitis virus vectors for detection of antigen-specific T cells.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Moseley Nelson B, Laur Oskar, Ibegbu Chris C, Loria Gilbert D, Ikwuenzunma Gini, Jayakar Himangi R, Whitt Michael A, Altman John D
Аннотация
Detection of antigen-specific T cells at the single-cell level by ELISpot or flow cytometry techniques employing intracellular cytokine staining (ICS) is now an indispensable tool in many areas of immunology. When precisely mapped, optimal MHC-binding peptide epitopes are unknown, these assays use antigen in a variety of forms, including recombinant proteins, overlapping peptide sets representing one or more target protein sequences, microbial lysates, lysates of microbially-infected cells, or gene delivery vectors such as DNA expression plasmids or recombinant vaccinia or adenoviruses expressing a target protein of interest. Here we introduce replication-restricted, recombinant vesicular stomatitis virus (VSV) vectors as a safe, easy to produce, simple to use, and highly effective vector for genetic antigen delivery for the detection of human antigen-specific helper and cytotoxic T cells. To demonstrate the broad applicability of this approach, we have used these vectors to detect human T cell responses to the immunodominant pp65 antigen of human cytomegalovirus, individual segments of the yellow fever virus polyprotein, and to various influenza proteins.
Предметные рубрики MeSH
AnimalsAntigens, ViralBrefeldin ACells, CulturedCricetinaeCytomegalovirusDNA ReplicationDendritic CellsGenetic VectorsHumansImmunodominant EpitopesInterferon-gammaLymphocyte ActivationMonocytesOrthomyxoviridaeT-Lymphocytes, CytotoxicT-Lymphocytes, Helper-InducerVesicular stomatitis Indiana virusViral ProteinsVirus ReplicationYellow fever virus