Influenza Vaccine in Lung Transplant Patients - Persistence of Antibodies Beyond the Season
Study Details
Study Description
Brief Summary
This a sub-study of a 5-year study designed to investigate how antibody and T cell responses following influenza vaccine compare among lung transplant patients, patients waiting for lung transplantation, and healthy individuals.
This study is designed to investigate influenza vaccine-induced antibodies in lung transplant patients beyond the season of vaccination.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
Every year influenza infection causes significant morbidity and mortality in the general population making it a serious public health concern. Among those at highest risk for complications from infection are the immunocompromised. Effective influenza immunization that confers protection throughout the season is critical for lung transplant recipients because in addition to aggressive immunosuppressive therapy, infection directly affects the transplanted organ. Studies of influenza vaccine response rates in lung transplant patients show generally lower antibody concentrations, but acceptable influenza vaccine response rates compared with healthy individuals. However, little is known about the persistence of influenza vaccine-induced antibody concentration in either healthy or immunosuppressed populations.
Influenza antibody concentrations persist at seroprotective levels (defined as antibody concentrations at least 40 hemagglutination units) up to a year post vaccination. However, the investigators could find no information regarding persistence beyond one year.
It is hypothesized that the high rates of persisting influenza vaccine antibody in immunosuppressed lung transplant individuals would match the rates of persisting vaccine-antibody in healthy individuals.
Influenza antibody concentrations against viruses no longer included in the vaccine were measured in serum by hemagglutination inhibition assay (HIA) annually (individual participants followed for 3 years). Samples were collected at 2-4 weeks post-vaccination. Seroprotection was defined as a titer of ≥ 1:40 and was compared between groups over the measured term using Fisher's exact tests.
[This substudy that was originally registered to NCT00205270 and subsequently registered to its own NCT number for the purpose of clarity in linked results]
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Vaccine, Post-transplant Cohort consist of individuals who have received lung transplants Inactivated influenza vaccine will be administered intramuscularly annually. |
Drug: Influenza vaccine
influenza vaccine 0.5 ml intramuscularly each season, antigens measured for 3 years following vaccination in:
2004-2005: A/Wyoming H3N2; B/Shanghai
2006-2007: A/New Caledonia H1N1
2007-2008: A/Solomon Islands; A/Wisconsin H3N2; B/Malaysia
|
| Vaccine, Healthy Control Cohort consists of healthy individuals who received the influenza vaccine Inactivated influenza vaccine will be administered intramuscularly annually. |
Drug: Influenza vaccine
influenza vaccine 0.5 ml intramuscularly each season, antigens measured for 3 years following vaccination in:
2004-2005: A/Wyoming H3N2; B/Shanghai
2006-2007: A/New Caledonia H1N1
2007-2008: A/Solomon Islands; A/Wisconsin H3N2; B/Malaysia
|
Outcome Measures
Primary Outcome Measures
- Antibody response to influenza vaccine [season 1 (up to 1 year on study)]
Influenza antibody concentrations against viruses no longer included in the vaccine were measured in serum by hemagglutination inhibition assay (HIA) annually following vaccination of lung transplant participants and healthy controls.
- Antibody response to influenza vaccine [season 2 (up to 2 years on study)]
Influenza antibody concentrations against viruses no longer included in the vaccine were measured in serum by hemagglutination inhibition assay (HIA) annually following vaccination of lung transplant participants and healthy controls.
- Antibody response to influenza vaccine [season 2 (up to 2.5 years on study)]
Influenza antibody concentrations against viruses no longer included in the vaccine were measured in serum by hemagglutination inhibition assay (HIA) annually following vaccination of lung transplant participants and healthy controls.
- Antibody response to influenza vaccine [season 3 (up to 3 years on study)]
Influenza antibody concentrations against viruses no longer included in the vaccine were measured in serum by hemagglutination inhibition assay (HIA) annually following vaccination of lung transplant participants and healthy controls.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Receiving care Post-lung transplant at University of Wisconsin Hospital
-
Healthy adult
Exclusion Criteria:
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Allergy to eggs
-
Moderate to severe febrile illness
-
Active treatment for acute rejection
-
Received season's influenza vaccine prior to enrollment
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Wisconsin | Madison | Wisconsin | United States | 53792 |
Sponsors and Collaborators
- University of Wisconsin, Madison
Investigators
- Principal Investigator: Mary S Hayney, PharmD, University of Wisconsin, Madison
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- H-2004-0240d
- A561000
- PHARM/PHARMACY/PHARMACY