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Clinical Trials/NCT03327987
NCT03327987
Withdrawn
Not Applicable

Safety and Immunogenicity of Influenza Vaccine During the First Post-Transplant Year in Solid Organ Transplant Recipients

University Health Network, Toronto1 site in 1 countryMay 7, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Influenza
Sponsor
University Health Network, Toronto
Locations
1
Primary Endpoint
Vaccine immunogenicity
Status
Withdrawn
Last Updated
5 years ago

Overview

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.

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).

Registry
clinicaltrials.gov
Start Date
May 7, 2019
End Date
May 7, 2019
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Kidney, liver or pancreas transplant recipients on at least one immunosuppressive medication
  • 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

Outcomes

Primary Outcomes

Vaccine immunogenicity

Time Frame: 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 Outcomes

  • Safety- adverse events(7 days)
  • Safety- graft rejection(6 months)
  • Safety- HLA(4 weeks)
  • Vaccine efficacy- CMI(4 weeks)
  • Vaccine efficacy- infection(6 months)

Study Sites (1)

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