HCV Virions Bound Proteins

NCT ID: NCT02795403

Last Updated: 2025-09-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-01-31
• Study Completion Date: 2015-07-31

Brief Summary

The emergence of hepatocellular carcinoma (HCC) has prompted a search for a thorough understanding of the biology of one of its major causative agents, the hepatitis C virus (HCV). HCV particles acquire via budding and encapsidation cellular proteins. There is mounting evidence on several viral species that virion-bound proteins are prone to be involved either at the replication, budding/egress or entry/release steps of the viral cycle.

Identifying such targets may yield ideal candidates for gaining insight on the dependence of HCV upon a restricted subset of host proteins, therefore providing refined sets of genetically stable targets for therapy. This project's goals are to set up adequate conditions for robust and reproducible purification of HCV virions in clinical samples, followed by the identification of their HCV-bound host proteins and the characterization of their functions. Proteomics profiling of HCV particles purified from clinical samples will be overlaid with proteins identified and characterized in cell culture grown HCV particles during my post-doctoral training, using clinical biomarker discovery grade criteria. Targets identified in both samples sets will be subjected to in vitro investigations using HCV-replicating cells. Conventional biochemical and imaging methods will be used in order to: (i) ascertain their physical association with HCV virions; (ii) define the modalities of their interaction with HCV proteins; (iii) decipher the topology and subcellular localization of their association with HCV proteins and virions; (iv) quantitatively assess their functional involvement in particle budding, egress or secretion and infectivity. A candidate that yielded satisfactory results in these experiments will be disclosed and further investigated at the level of structural biology, in collaborative research programs.

Conditions

Hepatitis C

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: SINGLE

Study Groups

Viraemic

Group Type: EXPERIMENTAL

blood draw of 150ml, twice

Intervention Type: OTHER

responder group

Group Type: EXPERIMENTAL

blood draw of 150ml, twice

Intervention Type: OTHER

Interventions

blood draw of 150ml, twice

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Adult> 18 and <60 years
• Infected with HCV genotype 1 HCV antibody positive.
• positive viremia for more than 6 months
• Viremia> 106 IU / ml.
• nonresponders to previous treatment and without antiviral treatment for 2 months.
• For control samples: Patients responders to previous treatment and without antiviral treatment for 2 months.

Exclusion Criteria

• Patient receiving or having received antiviral treatment within two months.
• patient with against-indication for a blood sample of 150 ml
• immunosuppressive therapy patient
• Patient with liver disease other than hepatitis C.
• Patients with cirrhosis.
• patient with hepatocellular carcinoma.
• Patients with one or more severe co-morbidities defined as:
• Co-infection with HIV or HBV.
• hematological malignancies changing or aplasia
• Insulin-dependent diabetes
• dialyzed chronic renal failure
• Heart failure
• Persons subject to legal protection or the subject of a safeguard measure of justice not affiliated with a social security scheme or not beneficiaries of such a scheme
• Pregnant women

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hospices Civils de Lyon

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Fabien ZOULIM, MD

Role: PRINCIPAL_INVESTIGATOR

Service d'Hépato-Gastroentérologie Lyon Croix-Rousse Hospices Civils de Lyon

Locations

Service d'Hépato-Gastroentérologie Lyon Croix-Rousse Hospices Civils de Lyon

Lyon, , France

Countries

France

References

Cottarel J, Plissonnier ML, Kullolli M, Pitteri S, Clement S, Millarte V, Si-Ahmed SN, Farhan H, Zoulim F, Parent R. FIG4 is a hepatitis C virus particle-bound protein implicated in virion morphogenesis and infectivity with cholesteryl ester modulation potential. J Gen Virol. 2016 Jan;97(1):69-81. doi: 10.1099/jgv.0.000331. Epub 2015 Oct 29.

Reference Type: BACKGROUND

PMID: 26519381 (View on PubMed)

Other Identifiers

2009-596

Identifier Type: -

Identifier Source: org_study_id