Early Flu Shots in SOT

Sponsor
University Health Network, Toronto (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03327987
Collaborator
(none)
0
1

Study Details

Study Description

Brief Summary

Although time from transplant has been a factor in vaccine response, there is limited data on immunizations that occur in the first post-transplant year, and there are no data that suggest influenza vaccination early post-transplant may have any adverse effects on the graft. It is suggested that early vaccinations may lead to reduced immunogenicity due to induction immunosuppression. However, not vaccinating patients may leave them vulnerable to influenza infection for a period of time. This study is designed to look at the immunogenicity and side effects of the standard of care influenza vaccine in patients between 31 and 365 days post-transplant.

Condition or Disease Intervention/Treatment Phase
  • Biological: standard of care influenza vaccine

Detailed Description

Influenza virus is an important cause of morbidity in the transplant population and can lead to viral and bacterial pneumonia. Influenza vaccine is effective in the prevention of influenza infection and is recommended by the Canadian National Advisory Committee on Immunization (NACI). The annual influenza vaccine is suggested for transplant patients as the standard of care starting from 3 months post-transplant. Most recent guidelines now suggest that it is reasonable to get a flu shot starting earlier at 1 month post-transplant. Anti-rejection drugs are now tapered more quickly and it is possible that antibodies will be produced against the flu shot as early as 1 month post-transplant. The study hypothesizes that kidney and liver transplant recipients in the early post-transplant period (31-180 days) will have similar immunogenicity as those in the late post-transplant period (>180 days).

Study Design

Study Type:
Observational
Actual Enrollment :
0 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Safety and Immunogenicity of Influenza Vaccine During the First Post-Transplant Year in Solid Organ Transplant Recipients
Actual Study Start Date :
May 7, 2019
Actual Primary Completion Date :
May 7, 2019
Actual Study Completion Date :
May 7, 2019

Arms and Interventions

Arm Intervention/Treatment
31-90 days

Patient 31-90 days after transplantation receiving standard of care annual 2017-2018 influenza vaccine.

Biological: standard of care influenza vaccine
The standard of care annual 2017-2018 influenza vaccine will be used for this study.
Other Names:
  • annual influenza vaccine
  • 91-180 days

    91-180 days after transplantation receiving standard of care annual 2017-2018 influenza vaccine.

    Biological: standard of care influenza vaccine
    The standard of care annual 2017-2018 influenza vaccine will be used for this study.
    Other Names:
  • annual influenza vaccine
  • 181-365 days

    181-365 days after transplantation receiving standard of care annual 2017-2018 influenza vaccine.

    Biological: standard of care influenza vaccine
    The standard of care annual 2017-2018 influenza vaccine will be used for this study.
    Other Names:
  • annual influenza vaccine
  • Outcome Measures

    Primary Outcome Measures

    1. Vaccine immunogenicity [4 weeks]

      Vaccine immunogenicity based on assessment of pre- and post-vaccine (4 weeks) antibody titer. A positive vaccine response will be defined based on: Seroconversion rate: serological response with a four-fold or greater increase in HAI antibody titers to each of the three antigens in the vaccine, and Seroprotection rate: HAI titers of ≥1:40 to each of the three antigens post-immunization.

    Secondary Outcome Measures

    1. Safety- adverse events [7 days]

      Local and systemic adverse events to vaccination

    2. Safety- graft rejection [6 months]

      Rates of biopsy proven allograft rejection in the 6 months following vaccination

    3. Safety- HLA [4 weeks]

      Development of de novo or increased titer of HLA alloantibody and specifically DSA (donor specific antibody). The 4 weeks post-vaccine sample will be compared with the pre-vaccine samples.

    4. Vaccine efficacy- CMI [4 weeks]

      Analysis of CMI in a subgroup of 60 patients (influenza strain-specific CD4+ and CD8+ T-cell responses; detectable vs. non-detectable and absolute percentage) at four weeks post-vaccine vs. pre-vaccine sample. CMI responses will also be correlated with HAI responses.

    5. Vaccine efficacy- infection [6 months]

      Documented influenza infection (i.e., microbiology proven by the direct fluorescent antibody, viral culture, or PCR) in the six months following vaccination.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Kidney, liver or pancreas transplant recipients on at least one immunosuppressive medication

    • Age ≥ 18

    • Outpatient status

    • Greater than 30 days post-transplant

    Exclusion Criteria:
    • Has already received influenza vaccination for 2017-2018 season

    • Egg allergy or allergy to previous influenza vaccine

    • Febrile illness in the past one week

    • Active Cytomegalovirus viremia

    • Use of Rituximab in the past one year

    • Ongoing or recent (in past 30 days) therapy for acute rejection

    • Chronic kidney insufficiency (creatinine clearance ≤30mL/min or dialysis-dependent

    • Previous life-threatening reaction to influenza vaccine (i.e., Guillain Barre Syndrome)

    • Receipt of intravenous immunoglobulin (IVIG) in the past 30 days or planning to receive IVIG in the next four weeks

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Health Network, Toronto General Hospital, Multi-Organ Transplant Toronto Ontario Canada M5G2N2

    Sponsors and Collaborators

    • University Health Network, Toronto

    Investigators

    • Principal Investigator: Deepali Kumar, MD, UHN

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Health Network, Toronto
    ClinicalTrials.gov Identifier:
    NCT03327987
    Other Study ID Numbers:
    • 17-5960
    First Posted:
    Nov 1, 2017
    Last Update Posted:
    Oct 20, 2020
    Last Verified:
    Oct 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University Health Network, Toronto
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 20, 2020