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HBV Virions Bound Proteins

Primary Purpose

Hepatitis B Virus Infection

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
blood draw
Sponsored by
Hospices Civils de Lyon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Hepatitis B Virus Infection focused on measuring HBV, liver

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Service d'Hépato-Gastroentérologie, Hopital de la Croix-Rousse, Hospices Civils de Lyon

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Viraemic

Remission

Arm Description

Outcomes

Primary Outcome Measures

Presence of a virion-bound protein identified by mass spectrometry

Secondary Outcome Measures

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.

Full Information

First Posted
May 30, 2016
Last Updated
September 11, 2018
Sponsor
Hospices Civils de Lyon
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1. Study Identification

Unique Protocol Identification Number
NCT02798549
Brief Title
HBV Virions Bound Proteins
Official Title
Hepatitis B Virus Particles-bound Human Proteins : Identification in Clinical Samples and Implication in the Viral Life Cycle
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
January 12, 2015 (Actual)
Primary Completion Date
January 2018 (Actual)
Study Completion Date
August 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospices Civils de Lyon

4. Oversight

Data Monitoring Committee
No

5. Study Description

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 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B Virus Infection
Keywords
HBV, liver

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Non-Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Viraemic
Arm Type
Other
Arm Title
Remission
Arm Type
Other
Intervention Type
Other
Intervention Name(s)
blood draw
Intervention Description
blood draw of 150ml, twice
Primary Outcome Measure Information:
Title
Presence of a virion-bound protein identified by mass spectrometry
Time Frame
One to two years after mass spectrometry identification of the candidate
Secondary Outcome Measure Information:
Title
Comparison of clinical virions datasets with in vitro grown virions datasets (mass spectrometry)
Description
Proteins identified from viral particles purified from clinical samples will be compared to proteins identified in viral particles from cells of human hepatocarcinoma origin.
Time Frame
One to two years after mass spectrometry identification of the candidate

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fabien Zoulim, Prof
Organizational Affiliation
Hospices Civils de Lyon, Univ. of Lyon, Inserm
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service d'Hépato-Gastroentérologie, Hopital de la Croix-Rousse, Hospices Civils de Lyon
City
Lyon
State/Province
Auvergne-Rhône-Alpes
ZIP/Postal Code
69004
Country
France

12. IPD Sharing Statement

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HBV Virions Bound Proteins

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