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Identification of Novel Yellow Fever Class II Epitopes in YF-17D Vaccinees
Yellow fever virus (YFV) is a mosquito-borne member of the genus flavivirus, including other important human-pathogenic viruses, such as dengue, Japanese encephalitis, and Zika. Herein, we report identifying 129 YFV Class II epitopes in donors vaccinated with the live attenuated YFV vaccine (YFV-17D...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697718/ https://www.ncbi.nlm.nih.gov/pubmed/33198381 http://dx.doi.org/10.3390/v12111300 |
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author | Mateus, Jose Grifoni, Alba Voic, Hannah Angelo, Michael A. Phillips, Elizabeth Mallal, Simon Sidney, John Sette, Alessandro Weiskopf, Daniela |
author_facet | Mateus, Jose Grifoni, Alba Voic, Hannah Angelo, Michael A. Phillips, Elizabeth Mallal, Simon Sidney, John Sette, Alessandro Weiskopf, Daniela |
author_sort | Mateus, Jose |
collection | PubMed |
description | Yellow fever virus (YFV) is a mosquito-borne member of the genus flavivirus, including other important human-pathogenic viruses, such as dengue, Japanese encephalitis, and Zika. Herein, we report identifying 129 YFV Class II epitopes in donors vaccinated with the live attenuated YFV vaccine (YFV-17D). A total of 1156 peptides predicted to bind 17 different common HLA-DRB1 allelic variants were tested using IFNγ ELISPOT assays in vitro re-stimulated peripheral blood mononuclear cells from twenty-six vaccinees. Overall, we detected responses against 215 YFV epitopes. We found that the capsid and envelope proteins, as well as the non-structural (NS) proteins NS3 and NS5, were the most targeted proteins by CD4(+) T cells from YF-VAX vaccinated donors. In addition, we designed and validated by flow cytometry a CD4(+) mega pool (MP) composed of structural and non-structural epitopes in an independent cohort of vaccinated donors. Overall, this study provides a comprehensive prediction and validation of YFV epitopes in a cohort of YF-17D vaccinated individuals. With the design of a CD4 epitope MP, we further provide a useful tool to detect ex vivo responses of YFV-specific CD4 T cells in small sample volumes. |
format | Online Article Text |
id | pubmed-7697718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76977182020-11-29 Identification of Novel Yellow Fever Class II Epitopes in YF-17D Vaccinees Mateus, Jose Grifoni, Alba Voic, Hannah Angelo, Michael A. Phillips, Elizabeth Mallal, Simon Sidney, John Sette, Alessandro Weiskopf, Daniela Viruses Article Yellow fever virus (YFV) is a mosquito-borne member of the genus flavivirus, including other important human-pathogenic viruses, such as dengue, Japanese encephalitis, and Zika. Herein, we report identifying 129 YFV Class II epitopes in donors vaccinated with the live attenuated YFV vaccine (YFV-17D). A total of 1156 peptides predicted to bind 17 different common HLA-DRB1 allelic variants were tested using IFNγ ELISPOT assays in vitro re-stimulated peripheral blood mononuclear cells from twenty-six vaccinees. Overall, we detected responses against 215 YFV epitopes. We found that the capsid and envelope proteins, as well as the non-structural (NS) proteins NS3 and NS5, were the most targeted proteins by CD4(+) T cells from YF-VAX vaccinated donors. In addition, we designed and validated by flow cytometry a CD4(+) mega pool (MP) composed of structural and non-structural epitopes in an independent cohort of vaccinated donors. Overall, this study provides a comprehensive prediction and validation of YFV epitopes in a cohort of YF-17D vaccinated individuals. With the design of a CD4 epitope MP, we further provide a useful tool to detect ex vivo responses of YFV-specific CD4 T cells in small sample volumes. MDPI 2020-11-12 /pmc/articles/PMC7697718/ /pubmed/33198381 http://dx.doi.org/10.3390/v12111300 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mateus, Jose Grifoni, Alba Voic, Hannah Angelo, Michael A. Phillips, Elizabeth Mallal, Simon Sidney, John Sette, Alessandro Weiskopf, Daniela Identification of Novel Yellow Fever Class II Epitopes in YF-17D Vaccinees |
title | Identification of Novel Yellow Fever Class II Epitopes in YF-17D Vaccinees |
title_full | Identification of Novel Yellow Fever Class II Epitopes in YF-17D Vaccinees |
title_fullStr | Identification of Novel Yellow Fever Class II Epitopes in YF-17D Vaccinees |
title_full_unstemmed | Identification of Novel Yellow Fever Class II Epitopes in YF-17D Vaccinees |
title_short | Identification of Novel Yellow Fever Class II Epitopes in YF-17D Vaccinees |
title_sort | identification of novel yellow fever class ii epitopes in yf-17d vaccinees |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697718/ https://www.ncbi.nlm.nih.gov/pubmed/33198381 http://dx.doi.org/10.3390/v12111300 |
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