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Flavivirus-induced antibody cross-reactivity
Dengue viruses (DENV) cause countless human deaths each year, whilst West Nile virus (WNV) has re-emerged as an important human pathogen. There are currently no WNV or DENV vaccines licensed for human use, yet vaccines exist against other flaviviruses. To investigate flavivirus cross-reactivity, ser...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Society for General Microbiology
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352572/ https://www.ncbi.nlm.nih.gov/pubmed/21900425 http://dx.doi.org/10.1099/vir.0.031641-0 |
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author | Mansfield, Karen L. Horton, Daniel L. Johnson, Nicholas Li, Li Barrett, Alan D. T. Smith, Derek J. Galbraith, Sareen E. Solomon, Tom Fooks, Anthony R. |
author_facet | Mansfield, Karen L. Horton, Daniel L. Johnson, Nicholas Li, Li Barrett, Alan D. T. Smith, Derek J. Galbraith, Sareen E. Solomon, Tom Fooks, Anthony R. |
author_sort | Mansfield, Karen L. |
collection | PubMed |
description | Dengue viruses (DENV) cause countless human deaths each year, whilst West Nile virus (WNV) has re-emerged as an important human pathogen. There are currently no WNV or DENV vaccines licensed for human use, yet vaccines exist against other flaviviruses. To investigate flavivirus cross-reactivity, sera from a human cohort with a history of vaccination against tick-borne encephalitis virus (TBEV), Japanese encephalitis virus (JEV) and yellow fever virus (YFV) were tested for antibodies by plaque reduction neutralization test. Neutralization of louping ill virus (LIV) occurred, but no significant neutralization of Murray Valley encephalitis virus was observed. Sera from some individuals vaccinated against TBEV and JEV neutralized WNV, which was enhanced by YFV vaccination in some recipients. Similarly, some individuals neutralized DENV-2, but this was not significantly influenced by YFV vaccination. Antigenic cartography techniques were used to generate a geometric illustration of the neutralization titres of selected sera against WNV, TBEV, JEV, LIV, YFV and DENV-2. This demonstrated the individual variation in antibody responses. Most sera had detectable titres against LIV and some had titres against WNV and DENV-2. Generally, LIV titres were similar to titres against TBEV, confirming the close antigenic relationship between TBEV and LIV. JEV was also antigenically closer to TBEV than WNV, using these sera. The use of sera from individuals vaccinated against multiple pathogens is unique relative to previous applications of antigenic cartography techniques. It is evident from these data that notable differences exist between amino acid sequence identity and mapped antigenic relationships within the family Flaviviridae. |
format | Online Article Text |
id | pubmed-3352572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Society for General Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-33525722012-05-29 Flavivirus-induced antibody cross-reactivity Mansfield, Karen L. Horton, Daniel L. Johnson, Nicholas Li, Li Barrett, Alan D. T. Smith, Derek J. Galbraith, Sareen E. Solomon, Tom Fooks, Anthony R. J Gen Virol Animal Dengue viruses (DENV) cause countless human deaths each year, whilst West Nile virus (WNV) has re-emerged as an important human pathogen. There are currently no WNV or DENV vaccines licensed for human use, yet vaccines exist against other flaviviruses. To investigate flavivirus cross-reactivity, sera from a human cohort with a history of vaccination against tick-borne encephalitis virus (TBEV), Japanese encephalitis virus (JEV) and yellow fever virus (YFV) were tested for antibodies by plaque reduction neutralization test. Neutralization of louping ill virus (LIV) occurred, but no significant neutralization of Murray Valley encephalitis virus was observed. Sera from some individuals vaccinated against TBEV and JEV neutralized WNV, which was enhanced by YFV vaccination in some recipients. Similarly, some individuals neutralized DENV-2, but this was not significantly influenced by YFV vaccination. Antigenic cartography techniques were used to generate a geometric illustration of the neutralization titres of selected sera against WNV, TBEV, JEV, LIV, YFV and DENV-2. This demonstrated the individual variation in antibody responses. Most sera had detectable titres against LIV and some had titres against WNV and DENV-2. Generally, LIV titres were similar to titres against TBEV, confirming the close antigenic relationship between TBEV and LIV. JEV was also antigenically closer to TBEV than WNV, using these sera. The use of sera from individuals vaccinated against multiple pathogens is unique relative to previous applications of antigenic cartography techniques. It is evident from these data that notable differences exist between amino acid sequence identity and mapped antigenic relationships within the family Flaviviridae. Society for General Microbiology 2011-12 /pmc/articles/PMC3352572/ /pubmed/21900425 http://dx.doi.org/10.1099/vir.0.031641-0 Text en © 2011 Crown copyright http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Animal Mansfield, Karen L. Horton, Daniel L. Johnson, Nicholas Li, Li Barrett, Alan D. T. Smith, Derek J. Galbraith, Sareen E. Solomon, Tom Fooks, Anthony R. Flavivirus-induced antibody cross-reactivity |
title | Flavivirus-induced antibody cross-reactivity |
title_full | Flavivirus-induced antibody cross-reactivity |
title_fullStr | Flavivirus-induced antibody cross-reactivity |
title_full_unstemmed | Flavivirus-induced antibody cross-reactivity |
title_short | Flavivirus-induced antibody cross-reactivity |
title_sort | flavivirus-induced antibody cross-reactivity |
topic | Animal |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352572/ https://www.ncbi.nlm.nih.gov/pubmed/21900425 http://dx.doi.org/10.1099/vir.0.031641-0 |
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