HBV Virions Bound Proteins

Hepatitis B Virus Infection Clinical Trial

Official title:

Hepatitis B Virus Particles-bound Human Proteins : Identification in Clinical Samples and Implication in the Viral Life Cycle

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02798549
• Other study ID #: 2013.809
• Status: Completed
• Phase: N/A
• Start date: January 12, 2015
• Est. completion date: August 2018

Study information

• Verified date: September 2018
• Source: Hospices Civils de Lyon
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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 B virus (HBV). HBV 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 HBV 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 HBV virions in clinical samples, followed by the identification of their HBV-bound host proteins and the characterization of their functions. Proteomics profiling of HBV particles purified from clinical samples will be overlaid with proteins identified and characterized in cell culture grown HBV particles, using clinical biomarker discovery grade criteria. Targets identified in both samples sets will be subjected to in vitro investigations using HBV-replicating cells. Conventional biochemical and imaging methods will be used in order to: (i) ascertain their physical association with HBV virions; (ii) define the modalities of their interaction with HBV proteins; (iii) decipher the topology and subcellular localization of their association with HBV 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 14
• Est. completion date: August 2018
• Est. primary completion date: January 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Inclusion criteria

• Adult> 18 and <60 years

• Infected with HBV.

• positive viremia for more than 6 months

• Viremia> 106 IU / ml.

• Immunotolerant individuals, untreated

• Aviraemic individuals,

Exclusion Criteria:

• patient with against-indication for a blood sample of 150 ml

• immunosuppressive therapy patient

• Patient with liver disease other than hepatitis B.

• patient with hepatocellular carcinoma.

• Patients with one or more severe co-morbidities defined as:

• Co-infection with HIV or hepatitis C virus (HCV).

• 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

Related Conditions & MeSH terms

• Hepatitis
• Hepatitis B
• Hepatitis B Virus Infection
• Virus Diseases

Intervention

Other:
• blood draw
blood draw of 150ml, twice

Locations

Country	Name	City	State
France	Service d'Hépato-Gastroentérologie, Hopital de la Croix-Rousse, Hospices Civils de Lyon	Lyon	Auvergne-Rhône-Alpes

Sponsors (1)

Lead Sponsor	Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Presence of a virion-bound protein identified by mass spectrometry		One to two years after mass spectrometry identification of the candidate
Secondary	Comparison of clinical virions datasets with in vitro grown virions datasets (mass spectrometry)	Proteins identified from viral particles purified from clinical samples will be compared to proteins identified in viral particles from cells of human hepatocarcinoma origin.	One to two years after mass spectrometry identification of the candidate