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Hepatitis B en Haitian Immigrants in Chile: Molecular Characterization and Determination of Vaccine Response

Primary Purpose

Hepatitis B

Status
Not yet recruiting
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Hepatitis B recombinant vaccine
Sponsored by
Pontificia Universidad Catolica de Chile
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hepatitis B focused on measuring hepatitis B, migration, HIV

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Adults (> 18 yo) born in Haiti.
  • Living in Chile (and planning to stay in Santiago for the next 4 months).

Exclusion Criteria:

  • Not signing the informed consent.
  • Pregnancy.
  • HIV or HCV infection.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Vaccine group

    Arm Description

    Administration of 3 doses hepatitis B vaccine (recombinant hepatitis B vaccine, injectable suspension for intramuscular use) at month 0, 1 and 2.

    Outcomes

    Primary Outcome Measures

    Response rate
    Developing antibodies against HBsAg (anti-HBs) > 10 mIU/mL

    Secondary Outcome Measures

    Full Information

    First Posted
    March 26, 2020
    Last Updated
    March 27, 2020
    Sponsor
    Pontificia Universidad Catolica de Chile
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04326803
    Brief Title
    Hepatitis B en Haitian Immigrants in Chile: Molecular Characterization and Determination of Vaccine Response
    Official Title
    Hepatitis B Virus (HBV) Infection in Haitian Immigrants in Chile: Determination of HBV Genotypes, Viral Escape Mutants and Host Factors Influencing Response to Vaccination
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2020
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    June 1, 2020 (Anticipated)
    Primary Completion Date
    June 30, 2022 (Anticipated)
    Study Completion Date
    December 30, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Pontificia Universidad Catolica de Chile

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    International migration to Chile has sharply increased since 2010. Particularly, Haitian migration now totals approximately 200.000 people. Preliminary results show a high prevalence of hepatitis B infection in this population. Approximately 35% of adult Haitian migrants in Chile have been exposed to hepatitis B infection. In this study the investigators aim to study the clinical and molecular characteristics of this infection and also to assess the serological response to an accelerated schedule of hepatitis B vaccination (0, 1 and 2 months).
    Detailed Description
    Migration from Haiti to Chile has increased exponentially in the last years. More than 200.000 people from this island are currently living in Chile. Preliminary results of the investigators group show that HIV infection and hepatitis B virus (HBV) infection are 2.9% and 2.4% (14 and 16 times higher than the reported prevalence in Chile), respectively, and overall HBV infection (anti-HBc antibody) is 34%. The molecular characterization of the HBV variants infecting people from Haiti has not been carried out. The current evidence suggests that HBV traveled from Africa together with the slave trade 200 to 300 years ago, with genotypes infecting Haitians resembling that of their origins, but with some striking differences, such as the presence of a recently described subtype (A5), which is now uncommon in Africa. HBV genotypes and subgenotypes may influence the emergence of specific mutations in the surface antigen region of the virus which in turn could lead to escape mutants which can infect properly vaccinated people. There is no information regarding the genotypes and escape mutants in Haitian immigrants to Chile. The most effective way to control and prevent is vaccination, but the response to vaccination varies widely in different ethnic groups, with genetic factors being relevant. Mutations in the interferon lambda 3 gene (IFNL3), previously known as interleukin 28B (IL28B) are clearly associated with lower response to interferon treatment and spontaneous clearance in hepatitis C, and clinical evolution of various viral infections. Less favorable IFNL3 mutations are especially prevalent in African descendants. The hypothesis of the project is that Haitian immigrants in Chile have a high prevalence of HBV infection with viral genotypes/mutations different from the native Chilean genotypes, which may result in a particular clinical presentation. The investigators also conjecture that the response to HBV vaccination may also differ in Haitian immigrants due to genetic variations in the IFNL3 gene. The HBV infection prevalence in this population will be estimated and the researchers will try to explain if mutations in IFNL3 increase the rate of spontaneous clearance of the infection (comparing carriers to patients who cleared the infection). They will also determine the presence of HBV DNA in all enrolled subjects to study the occurrence of occult hepatitis B (OBI), which is the presence of DNA in the absence of HBsAg. HBV DNA will be amplified and sequenced in the pre-S1, pre-S2 and S region (surface antigens) to study the presence of escape mutants. Finally, the investigators will conduct a study of vaccination of Haitian immigrants to assess the effectiveness of the vaccine in this population and determine which factors may influence vaccine response, including mutations in the IFNL3 gene. The information regarding the prevalence, epidemiology, presence of escape mutants, genetic factors influencing HBV infection and the response to the vaccine in Haitian immigrants, are critical for a better understanding of this infection and for the development of public health policies based on scientific evidence and not in political or other reasons that usually perpetuate stigma and inequalities in health care for marginalized groups.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Hepatitis B
    Keywords
    hepatitis B, migration, HIV

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 4
    Interventional Study Model
    Single Group Assignment
    Model Description
    A single group of subject will be offered to enroll in a study to assess the serological response to an accelerated schedule (0, 1 and 6 months) of recombinant hepatitis B vaccine
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    200 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Vaccine group
    Arm Type
    Experimental
    Arm Description
    Administration of 3 doses hepatitis B vaccine (recombinant hepatitis B vaccine, injectable suspension for intramuscular use) at month 0, 1 and 2.
    Intervention Type
    Biological
    Intervention Name(s)
    Hepatitis B recombinant vaccine
    Other Intervention Name(s)
    Engerix-B vaccine
    Intervention Description
    Administration of 20 mcg of hepatitis B recombinant vaccine im at month 0, 1 and 2
    Primary Outcome Measure Information:
    Title
    Response rate
    Description
    Developing antibodies against HBsAg (anti-HBs) > 10 mIU/mL
    Time Frame
    4-8 weeks after the third dose of the vaccine

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Adults (> 18 yo) born in Haiti. Living in Chile (and planning to stay in Santiago for the next 4 months). Exclusion Criteria: Not signing the informed consent. Pregnancy. HIV or HCV infection.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Ruth Núñez, RN
    Phone
    56223543820
    Email
    r.nunezpuentes@gmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Alejandro Soza, MD
    Organizational Affiliation
    Pontificia Universidad Catolica de Chile
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    Available on request
    Citations:
    PubMed Identifier
    26576083
    Citation
    Zampino R, Boemio A, Sagnelli C, Alessio L, Adinolfi LE, Sagnelli E, Coppola N. Hepatitis B virus burden in developing countries. World J Gastroenterol. 2015 Nov 14;21(42):11941-53. doi: 10.3748/wjg.v21.i42.11941.
    Results Reference
    background
    PubMed Identifier
    25920093
    Citation
    Locarnini S, Hatzakis A, Chen DS, Lok A. Strategies to control hepatitis B: Public policy, epidemiology, vaccine and drugs. J Hepatol. 2015 Apr;62(1 Suppl):S76-86. doi: 10.1016/j.jhep.2015.01.018.
    Results Reference
    background
    Links:
    URL
    http://hepatitis.cl
    Description
    Site in Spanish with information about viral hepatitis and liver diseases.

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    Hepatitis B en Haitian Immigrants in Chile: Molecular Characterization and Determination of Vaccine Response

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