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HBV Virions Bound Proteins

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Civil Hospices of Lyon

Status

Completed

Conditions

Hepatitis B Virus Infection

Treatments

Other: blood draw

Study type

Interventional

Funder types

Other

Identifiers

NCT02798549
2013.809

Details and patient eligibility

About

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.

Enrollment

14 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No 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

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

14 participants in 2 patient groups

Viraemic
Other group
Treatment:
Other: blood draw
Remission
Other group
Treatment:
Other: blood draw

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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