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Lack of immunodominance in the T cell response to herpes simplex virus glycoprotein D after administration of infectious virus
Glycoprotein D (gD) of HSV has been shown to be a potent immunogen. To analyze the T cell antigenic determinants on gD, a series of 28 overlapping 20-mer peptides that span the extracellular portion of gD-1 were examined for their ability to stimulate T cells from rgD-1 or infectious HSV-1-primed H-...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1989
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189426/ https://www.ncbi.nlm.nih.gov/pubmed/2475577 |
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collection | PubMed |
description | Glycoprotein D (gD) of HSV has been shown to be a potent immunogen. To analyze the T cell antigenic determinants on gD, a series of 28 overlapping 20-mer peptides that span the extracellular portion of gD-1 were examined for their ability to stimulate T cells from rgD-1 or infectious HSV-1-primed H-2d mice in vitro. rgD-1-primed cells responded exclusively to peptide 241-260, the immunodominant determinant of gD in H-2d mice. In contrast, infectious HSV-primed T cells were shown to respond to 17 (and up to 22) of 28 synthetic gD peptides. These results indicate an extensive diversity in the T cell repertoire to gD in H-2d mice with T cells directed to a broad array of peptide determinants being recruited during the acute phase of an HSV infection. |
format | Text |
id | pubmed-2189426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21894262008-04-17 Lack of immunodominance in the T cell response to herpes simplex virus glycoprotein D after administration of infectious virus J Exp Med Articles Glycoprotein D (gD) of HSV has been shown to be a potent immunogen. To analyze the T cell antigenic determinants on gD, a series of 28 overlapping 20-mer peptides that span the extracellular portion of gD-1 were examined for their ability to stimulate T cells from rgD-1 or infectious HSV-1-primed H-2d mice in vitro. rgD-1-primed cells responded exclusively to peptide 241-260, the immunodominant determinant of gD in H-2d mice. In contrast, infectious HSV-primed T cells were shown to respond to 17 (and up to 22) of 28 synthetic gD peptides. These results indicate an extensive diversity in the T cell repertoire to gD in H-2d mice with T cells directed to a broad array of peptide determinants being recruited during the acute phase of an HSV infection. The Rockefeller University Press 1989-09-01 /pmc/articles/PMC2189426/ /pubmed/2475577 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Lack of immunodominance in the T cell response to herpes simplex virus glycoprotein D after administration of infectious virus |
title | Lack of immunodominance in the T cell response to herpes simplex virus glycoprotein D after administration of infectious virus |
title_full | Lack of immunodominance in the T cell response to herpes simplex virus glycoprotein D after administration of infectious virus |
title_fullStr | Lack of immunodominance in the T cell response to herpes simplex virus glycoprotein D after administration of infectious virus |
title_full_unstemmed | Lack of immunodominance in the T cell response to herpes simplex virus glycoprotein D after administration of infectious virus |
title_short | Lack of immunodominance in the T cell response to herpes simplex virus glycoprotein D after administration of infectious virus |
title_sort | lack of immunodominance in the t cell response to herpes simplex virus glycoprotein d after administration of infectious virus |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189426/ https://www.ncbi.nlm.nih.gov/pubmed/2475577 |