To Include or Occlude: Rational Engineering of HCV Vaccines for Humoral Immunity

Direct-acting antiviral agents have proven highly effective at treating existing hepatitis C infections but despite their availability most countries will not reach the World Health Organization targets for elimination of HCV by 2030. A prophylactic vaccine remains a high priority. Whilst early vacc...

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Main Authors: Felicia Schlotthauer, Joey McGregor, Heidi E Drummer
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/13/5/805
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author Felicia Schlotthauer
Joey McGregor
Heidi E Drummer
author_facet Felicia Schlotthauer
Joey McGregor
Heidi E Drummer
author_sort Felicia Schlotthauer
collection DOAJ
description Direct-acting antiviral agents have proven highly effective at treating existing hepatitis C infections but despite their availability most countries will not reach the World Health Organization targets for elimination of HCV by 2030. A prophylactic vaccine remains a high priority. Whilst early vaccines focused largely on generating T cell immunity, attention is now aimed at vaccines that generate humoral immunity, either alone or in combination with T cell-based vaccines. High-resolution structures of hepatitis C viral glycoproteins and their interaction with monoclonal antibodies isolated from both cleared and chronically infected people, together with advances in vaccine technologies, provide new avenues for vaccine development.
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spelling doaj.art-05c2224d4bb142338bc23d72e251a2ff2023-11-21T18:04:08ZengMDPI AGViruses1999-49152021-04-0113580510.3390/v13050805To Include or Occlude: Rational Engineering of HCV Vaccines for Humoral ImmunityFelicia Schlotthauer0Joey McGregor1Heidi E Drummer2Viral Entry and Vaccines Group, Burnet Institute, Melbourne, VIC 3004, AustraliaViral Entry and Vaccines Group, Burnet Institute, Melbourne, VIC 3004, AustraliaViral Entry and Vaccines Group, Burnet Institute, Melbourne, VIC 3004, AustraliaDirect-acting antiviral agents have proven highly effective at treating existing hepatitis C infections but despite their availability most countries will not reach the World Health Organization targets for elimination of HCV by 2030. A prophylactic vaccine remains a high priority. Whilst early vaccines focused largely on generating T cell immunity, attention is now aimed at vaccines that generate humoral immunity, either alone or in combination with T cell-based vaccines. High-resolution structures of hepatitis C viral glycoproteins and their interaction with monoclonal antibodies isolated from both cleared and chronically infected people, together with advances in vaccine technologies, provide new avenues for vaccine development.https://www.mdpi.com/1999-4915/13/5/805glycoprotein E2vaccine developmenthumoral immunity
spellingShingle Felicia Schlotthauer
Joey McGregor
Heidi E Drummer
To Include or Occlude: Rational Engineering of HCV Vaccines for Humoral Immunity
Viruses
glycoprotein E2
vaccine development
humoral immunity
title To Include or Occlude: Rational Engineering of HCV Vaccines for Humoral Immunity
title_full To Include or Occlude: Rational Engineering of HCV Vaccines for Humoral Immunity
title_fullStr To Include or Occlude: Rational Engineering of HCV Vaccines for Humoral Immunity
title_full_unstemmed To Include or Occlude: Rational Engineering of HCV Vaccines for Humoral Immunity
title_short To Include or Occlude: Rational Engineering of HCV Vaccines for Humoral Immunity
title_sort to include or occlude rational engineering of hcv vaccines for humoral immunity
topic glycoprotein E2
vaccine development
humoral immunity
url https://www.mdpi.com/1999-4915/13/5/805
work_keys_str_mv AT feliciaschlotthauer toincludeoroccluderationalengineeringofhcvvaccinesforhumoralimmunity
AT joeymcgregor toincludeoroccluderationalengineeringofhcvvaccinesforhumoralimmunity
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