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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.

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