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Influenza Immunization in Adults Over Age 75

Primary Purpose

Influenza, Immunization, Older Adults

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Influenza
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Influenza

Eligibility Criteria

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

Inclusion Criteria:

  • Adults over age 75 years

Exclusion Criteria:

  • Allergies to egg or vaccine
  • Active malignancies
  • On radiation or chemotherapy
  • Active systemic inflammatory diseases including rheumatoid arthritis, Crohn's disease, and ulcerative colitis
  • Acute exacerbation of chronic cardiopulmonary conditions including decompensated CHF or COPD
  • Taking oral steroids (such as prednisone) or immune modulating drugs (such as methotrexate).
  • Lacking the capacity to consent (individuals who do not understand what Flu shot is or need someone else to decide if s/he should get the Flu shot)

Sites / Locations

  • Johns Hopkins University; JHAAC 5501 Hopkins Bayview Circle, 1B84Recruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Influenza Immunization

Arm Description

Influenza immunization in adults over age 75

Outcomes

Primary Outcome Measures

Presence of CMV Viral DNA in Peripheral Blood Monocytes
To assess the role of chronic CMV infection as defined by presence of CMV viral DNA in peripheral monocytes as a risk factor for vaccine failure in this oldest old subset.

Secondary Outcome Measures

Immune Responses to High Dose TIV Immunization

Full Information

First Posted
July 11, 2014
Last Updated
April 19, 2023
Sponsor
Johns Hopkins University
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1. Study Identification

Unique Protocol Identification Number
NCT02200276
Brief Title
Influenza Immunization in Adults Over Age 75
Official Title
Influenza Immunization in Adults Over Age 75
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 2014 (undefined)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
June 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The immune system is the part of the body that protects against infection. The immune system often doesn't work as effectively as people get older. This research is being done to find out how the immune systems in older people who are over age 75 respond to influenza vaccine (flu shot). We also want to find out if chronic cytomegalovirus (CMV) infection, a common virus infection in older persons affects the immune response in people older than 75 years of age who receive a flu shot. The Flu Shot is a vaccine approved for the prevention of influenza ("Flu") infections and is recommended every year for all persons 50 years and older. People who are older than 75 years of age are considered healthy or frail may join. A total of 1025 persons will be participating in this study. In order to determine if you are qualified for the study, we would ask you to answer a few questions over the phone that will take approximately 5 minutes. If you qualify and agree to proceed, you will be asked to come to Johns Hopkins Bayview Medical Center or, if you are unable to come to Bayview, one of our staff can visit you at your home. During that visit we obtain consent, review your medical history, and measure your vital signs, walking speed and grip strength. We will also administer a few brief questionnaires and collect urine and blood samples. We will then give you the Influenza vaccine for free. 7 days post receiving your Influenza Vaccine we will collect a small blood sample for further immune system testing. also, you will be asked to complete a 12-question survey which will assess your symptoms over the past 7 days (post receiving the Influenza vaccine). Also 4 weeks post receiving your Influenza vaccine you will be asked to complete a third visit that will include follow up health questionnaires and an influenza symptoms assessment questionnaire and vital signs. A third blood draw will be collected (approximately 10 teaspoons) to measure immune responses to the influenza vaccine. In addition, you will receive your test result (CBC/w/Diff.) from visit #1. Throughout the influenza study season, we will call you once a week to ask about your general health and any Flu-like symptoms. These calls will be made throughout the Flu season which typically lasts through May. If you begin to have any influenza like symptoms at any time during the study, we ask that you call our office to report these symptoms so that we may perform vital signs, nasal swab to confirm influenza, and a fourth blood draw to look at the immune response and protection of influenza vaccine.
Detailed Description
Seasonal influenza causes significant morbidity and mortality and is the fourth leading cause of death for older Americans. Annual immunization with a trivalent inactivated influenza vaccine (TIV) is recommended for all adults 50 years and older. However, despite improved vaccination coverage in older adults over time, influenza-related mortality has actually increased. While many TIV studies indicate its benefit for older adults as a whole, these studies lacked representation of the older and frail subset of the elderly who suffer over three-quarters of influenza-related mortality. Our pilot study funded by a Beeson K23 award showed significant vaccine failures in both antibody response to TIV and clinical protection in the frail elderly. Our preliminary data also suggest that chronic cytomegalovirus (CMV) infection as defined by the presence of CMV viral DNA in peripheral monocytes using a highly sensitive and specific nested PCR-based assay developed in our laboratory, rather than anti-CMV IgG serology, is associated with poor antibody and T-cell responses to TIV immunization as well as poor clinical protection. This is likely because anti-CMV IgG serology, the conventional diagnostic measure for chronic CMV infection, is a crude measure that merely indicates prior exposure to CMV and does not distinguish chronic (persistent) from past (resolved) infections. Mechanistically, precipitous immune functional decline has been observed in those over 75 and chronic CMV infection may contribute significantly to age-related immune senescent remodeling, termed immunosenescence. In order to improve our assessment of the effectiveness of TIV immunization and understanding of risk factors and underlying immune mechanisms that determine vaccine failure in adults over age 75, the frail, oldest old adult subset, this study is designed to conduct prospective, 4-year TIV immunization and post-vaccination influenza surveillance in adults over 75 years. We will first assess chronic CMV infection defined by detectable CMV DNA in peripheral blood monocytes and frailty status of the study participants and administer the Fluzone High-Dose TIV vaccine. Influenza-like illness (ILI) cases will be identified through post-vaccination influenza surveillance as previously done in the Beeson project and respiratory specimens obtained from ILI cases will be tested using the cutting edge PCR-based IBIS assay which can accurately subtype influenza and other respiratory viruses in the laboratory of Dr. Charlotte Gaydos in Division of Infectious Disease, a co-investigator of this project. Strain-specific antibody responses to TIV immunization will be measured by the standard hemogglutination inhibition (HI) assay. We will also evaluate T-cell responses to influenza viruses at baseline and after TIV immunization. Taken together, these studies will provide more accurate assessment of the clinical effectiveness of TIV immunization in real world geriatric population over age 75 and its underlying humoral and cell-mediated immune mechanisms. Moreover, we investigate the role of chronic CMV infection as defined by the presence of CMV viral DNA in peripheral monocytes as a risk factor for vaccine failure in the elderly over age 75. Because this oldest old subset is growing most rapidly in numbers and is at greatest risk for influenza-related morbidity and mortality. The long-term goal of this research is to strengthen immune protection against influenza for vulnerable older Americans through more effective and targeted immunization strategies as well as possibly through prevention and mitigation of chronic CMV infection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Influenza, Immunization, Older Adults, Over Age 75

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
1025 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Influenza Immunization
Arm Type
Other
Arm Description
Influenza immunization in adults over age 75
Intervention Type
Biological
Intervention Name(s)
Influenza
Primary Outcome Measure Information:
Title
Presence of CMV Viral DNA in Peripheral Blood Monocytes
Description
To assess the role of chronic CMV infection as defined by presence of CMV viral DNA in peripheral monocytes as a risk factor for vaccine failure in this oldest old subset.
Time Frame
At the end of each flu season for the next 4 years
Secondary Outcome Measure Information:
Title
Immune Responses to High Dose TIV Immunization
Time Frame
At the end of the study-5th year
Other Pre-specified Outcome Measures:
Title
Effectiveness of High Dose TIV Immunization
Description
To assess clinical effectiveness of High Dose TIV immunization in real world geriatric population over age 75 through post-vaccination influenza detection
Time Frame
At the end of the study, 5th year
Title
Influence of Frailty and Chronic CMV Infection on Vaccine-Induced Influenza Strain-Specific Antibody Titers and T-Cell Responses
Description
To assess potential interaction between chronic CMV infection as defined above and frailty in their impact on antibody and T-cell responses to as well as clinical protection of High Dose TIV immunization in the study population.
Time Frame
At the end of the study, 5th year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adults over age 75 years Exclusion Criteria: Allergies to egg or vaccine Active malignancies On radiation or chemotherapy Active systemic inflammatory diseases including rheumatoid arthritis, Crohn's disease, and ulcerative colitis Acute exacerbation of chronic cardiopulmonary conditions including decompensated CHF or COPD Taking oral steroids (such as prednisone) or immune modulating drugs (such as methotrexate). Lacking the capacity to consent (individuals who do not understand what Flu shot is or need someone else to decide if s/he should get the Flu shot)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Engle Abrams
Phone
410-550-2061
Email
eabrams3@jhmi.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Janna Shapiro
Phone
410-550-2061
Email
jshapi30@jh.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sean Leng
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins University; JHAAC 5501 Hopkins Bayview Circle, 1B84
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Engle Abrams
Phone
410-550-2061
Email
eabrams3@jhmi.edu
First Name & Middle Initial & Last Name & Degree
Trudymae Agboka, M.S. Biology
Phone
410-550-6763
Email
Tagboka1@jhmi.edu
First Name & Middle Initial & Last Name & Degree
Sean Leng, MD, PhD

12. IPD Sharing Statement

Learn more about this trial

Influenza Immunization in Adults Over Age 75

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