| Literature DB >> 33946211 |
Felicia Schlotthauer1,2, Joey McGregor1,2, Heidi E Drummer1,2,3.
Abstract
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.Entities:
Keywords: glycoprotein E2; humoral immunity; vaccine development
Year: 2021 PMID: 33946211 DOI: 10.3390/v13050805
Source DB: PubMed Journal: Viruses ISSN: 1999-4915 Impact factor: 5.048