Back to results

UNSW, Sydney

Resistance to hepatitis C virus : potential genetic and immunological determinants

Abstract

dc:description

Studies of highly exposed individuals who remain seronegative (HESN) for HIV infection led to the discovery that homozygosity for the d32 mutation in the CCR5 chemokine receptor gene abrogated viral entry into target cells, and was associated with resistance to infection. In addition, evidence for protective immunity has been found in some HESN groups, such as sex workers in the Gambia. Population studies of those at high risk for hepatitis C virus (HCV) infection suggest that a HESN phenotype exists. There is a growing body of evidence for protective immunity, which allows clearance of HCV without seroconversion, and proof-of-principle evidence from in vitro studies that genetic polymorphisms may confer resistance to establishment of infection. This doctoral research project explores evidence for protective immunity, including via genetically programmed variations in host responses and provides evidence that genetic mutations confer resistance against HCV. The data generally strengthens the notion that investigations of naturally occurring polymorphisms within the HCV interactome, and genetic association studies of well-characterised HESN individuals, may identify potential targets for vaccine design and inform novel therapies.

Degree

thesis:*
Grantor dc:publisher
UNSW, Sydney
Year dc:date
2021

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Mina, Michael

Subjects

dc:subject × 3

Rights

dc:rights
Statement dc:rights
  • open access
  • CC BY-NC-ND 3.0
  • free_to_read
Language dc:language
EN

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:unsworks.library.unsw.edu.au:1959.4/70671

Chain of custody

source
Harvested from
University of New South Wales
Base URL
unsworks.unsw.edu.au/oai/provider
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Mina, Michael. Resistance to hepatitis C virus : potential genetic and immunological determinants. UNSW, Sydney, 2021. http://hdl.handle.net/1959.4/70671