An In-Depth Analysis of Original Antigenic Sin in Dengue Virus Infection

The evolution of dengue viruses has resulted in four antigenically similar yet distinct serotypes. Infection with one serotype likely elicits lifelong immunity to that serotype, but generally not against the other three. Secondary or sequential infections are common, as multiple viral serotypes freq...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
1. Verfasser: Simmons, Cameron
Format: Journal Article
Sprache:Englisch
Veröffentlicht: 2018
Online-Zugang:https://demo7.dspace.org/handle/123456789/84
Tags: Tag hinzufügen
Keine Tags, Fügen Sie das erste Tag hinzu!
_version_ 1860822454794977280
author Simmons, Cameron
author_browse Simmons, Cameron
author_facet Simmons, Cameron
author_sort Simmons, Cameron
collection DSpace
description The evolution of dengue viruses has resulted in four antigenically similar yet distinct serotypes. Infection with one serotype likely elicits lifelong immunity to that serotype, but generally not against the other three. Secondary or sequential infections are common, as multiple viral serotypes frequently cocirculate. Dengue infection, although frequently mild, can lead to dengue hemorrhagic fever (DHF) which can be life threatening. DHF is more common in secondary dengue infections, implying a role for the adaptive immune response in the disease. There is currently much effort toward the design and implementation of a dengue vaccine but these efforts are made more difficult by the challenge of inducing durable neutralizing immunity to all four viruses. Domain 3 of the dengue virus envelope protein (ED3) has been suggested as one such candidate because it contains neutralizing epitopes and it was originally thought that relatively few cross-reactive antibodies are directed to this domain. In this study, we performed a detailed analysis of the anti-ED3 response in a cohort of patients suffering either primary or secondary dengue infections. The results show dramatic evidence of original antigenic sin in secondary infections both in terms of binding and enhancement activity. This has important implications for dengue vaccine design because heterologous boosting is likely to maintain the immunological footprint of the first vaccination. On the basis of these findings, we propose a simple in vitro enzyme-linked immunosorbent assay (ELISA) to diagnose the original dengue infection in secondary dengue cases.
format Journal Article
id oai:localhost:123456789-84
institution DSPACE.FCHPT
language English
publishDate 2018
publishDateRange 2018
publishDateSort 2018
record_format dspace
spelling oai:localhost:123456789-842021-04-07T16:30:07Z An In-Depth Analysis of Original Antigenic Sin in Dengue Virus Infection Simmons, Cameron The evolution of dengue viruses has resulted in four antigenically similar yet distinct serotypes. Infection with one serotype likely elicits lifelong immunity to that serotype, but generally not against the other three. Secondary or sequential infections are common, as multiple viral serotypes frequently cocirculate. Dengue infection, although frequently mild, can lead to dengue hemorrhagic fever (DHF) which can be life threatening. DHF is more common in secondary dengue infections, implying a role for the adaptive immune response in the disease. There is currently much effort toward the design and implementation of a dengue vaccine but these efforts are made more difficult by the challenge of inducing durable neutralizing immunity to all four viruses. Domain 3 of the dengue virus envelope protein (ED3) has been suggested as one such candidate because it contains neutralizing epitopes and it was originally thought that relatively few cross-reactive antibodies are directed to this domain. In this study, we performed a detailed analysis of the anti-ED3 response in a cohort of patients suffering either primary or secondary dengue infections. The results show dramatic evidence of original antigenic sin in secondary infections both in terms of binding and enhancement activity. This has important implications for dengue vaccine design because heterologous boosting is likely to maintain the immunological footprint of the first vaccination. On the basis of these findings, we propose a simple in vitro enzyme-linked immunosorbent assay (ELISA) to diagnose the original dengue infection in secondary dengue cases. 2018-09-14T11:14:52Z 2017-07-12T05:09:52Z 2018-09-14T11:14:52Z 2011-01-01 Journal Article https://demo7.dspace.org/handle/123456789/84 English
spellingShingle Simmons, Cameron
An In-Depth Analysis of Original Antigenic Sin in Dengue Virus Infection
title An In-Depth Analysis of Original Antigenic Sin in Dengue Virus Infection
title_full An In-Depth Analysis of Original Antigenic Sin in Dengue Virus Infection
title_fullStr An In-Depth Analysis of Original Antigenic Sin in Dengue Virus Infection
title_full_unstemmed An In-Depth Analysis of Original Antigenic Sin in Dengue Virus Infection
title_short An In-Depth Analysis of Original Antigenic Sin in Dengue Virus Infection
title_sort in depth analysis of original antigenic sin in dengue virus infection
url https://demo7.dspace.org/handle/123456789/84
work_keys_str_mv AT simmonscameron anindepthanalysisoforiginalantigenicsinindenguevirusinfection
AT simmonscameron indepthanalysisoforiginalantigenicsinindenguevirusinfection