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Cell Mediated Immunity in Older Adults (CMI)

Primary Purpose

Immunity to Influenza Vaccine

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
High dose influenza vaccine Sanofi-Pasteur
fluzone by sanofi pasteur
Sponsored by
Vanderbilt University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Immunity to Influenza Vaccine focused on measuring influenza, vaccine, cell mediated immunity, elderly, high dose influenza vaccine

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • healthy
  • aged 65+ years

Exclusion Criteria:

  • <65 years
  • influenza vaccine allergy
  • Guillain-Barre
  • weight <110 pounds

Sites / Locations

  • Vanderbilt University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Standard dose influenza vaccine

High Dose Vaccine

Arm Description

Fluzone (Sanofi Pasteur)

High Dose Fluzone by sanofi pasteur

Outcomes

Primary Outcome Measures

Cellular Immune Response
comparison of CMI in high vs standard dose

Secondary Outcome Measures

Antibody Responses
Hemagglutination inhibition antibody titers measured for standard vs high dose

Full Information

First Posted
August 23, 2010
Last Updated
April 3, 2014
Sponsor
Vanderbilt University
Collaborators
Centers for Disease Control and Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT01189123
Brief Title
Cell Mediated Immunity in Older Adults
Acronym
CMI
Official Title
Evaluation of Cell-mediated Immunity and Antibody Response to Influenza Vaccination and Correlates of Protection in Seniors
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
August 2010 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
August 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University
Collaborators
Centers for Disease Control and Prevention

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is to study the immune response to the flu vaccine in people 65 years old and older. Only adults 65 years old and older and who are getting their flu vaccine are being asked to join in this study. The investigators plan to enroll approximately 100 people in this study in the 2010-2011 flu season. Vanderbilt is working with the Centers for Disease Control and Prevention on this study. There will be 5 study visits. Up to 4 tablespoons of blood from a vein will be obtained prior to the flu shot. Return visits will be 1, 2, and 4 weeks later,with up to 4 tablespoons of blood drawn again. Patients will be randomized to receive either the standard dose or the high dose flu vaccine. Both flu vaccines are FDA-approved.
Detailed Description
During the 2010-2011 influenza season, approximately 100 adults ≥65 years of age will be enrolled. After consent, blood and serum will be collected and then subjects will be randomized to either standard or high dose influenza vaccine (both FDA approved vaccines). Vaccination will be done by an unblinded nurse. All further evaluations and analysis will be done by a blinded staff member. Medical history, relevant medications, and functional/nutritional status will be assessed at the first visit. Subjects will return (Table 3) for blood and serum draws on days 7, 14, 28 and for a serum blood draw after influenza season. No micronutrient samples will be drawn, but serum will be kept for possible vitamin D testing. During influenza season, subjects will answer a questionnaire about influenza-like illness (ILI) every two weeks (either by email or telephone) and will be asked to return for a nasal swab if an ILI is present. Comparisons will be made of the cell-mediated response of those vaccinated with standard versus high dose vaccines. Analyses will be done accounting for age, use of immunomodulating agents, and underlying medical conditions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Immunity to Influenza Vaccine
Keywords
influenza, vaccine, cell mediated immunity, elderly, high dose influenza vaccine

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
105 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard dose influenza vaccine
Arm Type
Active Comparator
Arm Description
Fluzone (Sanofi Pasteur)
Arm Title
High Dose Vaccine
Arm Type
Active Comparator
Arm Description
High Dose Fluzone by sanofi pasteur
Intervention Type
Biological
Intervention Name(s)
High dose influenza vaccine Sanofi-Pasteur
Other Intervention Name(s)
High dose fluzone (Sanofi-Pasteur)
Intervention Description
High dose influenza vaccine Sanofi-Pasteur at standard dosing intramuscular injection
Intervention Type
Biological
Intervention Name(s)
fluzone by sanofi pasteur
Intervention Description
standard dose fluzone
Primary Outcome Measure Information:
Title
Cellular Immune Response
Description
comparison of CMI in high vs standard dose
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Antibody Responses
Description
Hemagglutination inhibition antibody titers measured for standard vs high dose
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: healthy aged 65+ years Exclusion Criteria: <65 years influenza vaccine allergy Guillain-Barre weight <110 pounds
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
H. Keipp Talbot, MD MPH
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vanderbilt University Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37215
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
27473306
Citation
Kim JH, Talbot HK, Mishina M, Zhu Y, Chen J, Cao W, Reber AJ, Griffin MR, Shay DK, Spencer SM, Sambhara S. High-dose influenza vaccine favors acute plasmablast responses rather than long-term cellular responses. Vaccine. 2016 Aug 31;34(38):4594-4601. doi: 10.1016/j.vaccine.2016.07.018. Epub 2016 Jul 26.
Results Reference
derived

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Cell Mediated Immunity in Older Adults

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