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Adacel® Booster Vaccination for CMI Assay Development

Primary Purpose

Pertussis

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Adacel®
Sponsored by
Dalhousie University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pertussis

Eligibility Criteria

17 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age ≥16years
  • Primed during infancy with an acellular pertussis vaccine
  • Good general health status, as determined by history no greater than 30 days prior to administration of the first test article
  • Written informed consent provided
  • If female of child-bearing potential, has a negative pregnancy test on the day of consent and has agreed to continue adequate contraception until after the last blood draw.

Exclusion Criteria:

  • Not primed in infancy with an acellular pertussis vaccine
  • History of anemia
  • Underlying chronic medical condition requiring ongoing monitoring by a physician (e.g., diabetes, seizure disorder)
  • Underlying cardiac and/or pulmonary disease including hypertension, angina, prior myocardial infection, asthma, emphysema, chronic bronchitis, and pulmonary tuberculosis
  • Pregnant (known before or established at the time of screening using a urine-based test)
  • Immunocompromised (reporting HIV/AIDS positive or receiving immunosuppressive therapy involving steroids)
  • Vaccinated against pertussis within previous 5 years
  • Refusing to get an Adacel® (TdaP) vaccination dose

Sites / Locations

  • Canadian Center for Vaccinology

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Adacel®

Arm Description

All participants will receive one booster dose of commercially available Adacel® (TdaP-Tetanus, diphtheria, acellular pertussis) vaccine

Outcomes

Primary Outcome Measures

Determine best assay to evaluate CMI responses post-vaccination: CD4 T-cell proliferation
% CD4+CTV-T cells analyzed by flow cytometry
Determine best assay to evaluate CMI responses post-vaccination: CD8 T-cell proliferation
% CD8+ CTV-T cells analyzed by flow cytometry
Determine optimal time point for sample collection: CD4 T-cell responses
% CD4+CTV-cytokine+T cells analyzed by flow cytometry
Determine optimal time point for sample collection: CD8 T-cell responses
% CD8+ CTV-cytokine+T cells analyzed by flow cytometry

Secondary Outcome Measures

Transcriptomic profiling of host - B. pertussis antigen interactions: B-cell plasmablasts
ASC per 106 PBMCs (ELISpot)
Transcriptomic profiling of host - B. pertussis antigen interactions: B-cell plasmablasts
% CD19+ CD38+ CD27+ cells

Full Information

First Posted
April 26, 2017
Last Updated
September 9, 2020
Sponsor
Dalhousie University
Collaborators
Sanofi Pasteur, a Sanofi Company, VaxDesign Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT04543669
Brief Title
Adacel® Booster Vaccination for CMI Assay Development
Official Title
Adacel® (TdaP-Tetanus, Diphtheria, Acellular Pertussis) Booster Vaccination of Acellular Pertussis Vaccine-primed Individuals for Cell Mediated Immunity Assay Development
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
July 12, 2017 (Actual)
Primary Completion Date
September 20, 2017 (Actual)
Study Completion Date
September 20, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dalhousie University
Collaborators
Sanofi Pasteur, a Sanofi Company, VaxDesign Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Recruitment of individuals primed during childhood with TdaP (tetanus, diphtheria , acellular pertussis) vaccine, and administration of an Adacel booster with blood sample collection at various time points before and after vaccination. Collection of blood sample volumes will be large enough to allow assessment and comparison of multiple assays that evaluate cell-mediated immune (CMI) responses and other biomarkers following the administration of pertussis vaccinations. The ultimate objective would be to utilize these validated assays for evaluation of pertussis clinical trial results or development of new pertussis vaccine formulations.
Detailed Description
Pertussis, known as "whooping cough", is caused by the bacterium Bordetella pertussis which was discovered over a century ago. Human vaccines were developed in the subsequent two decades and routine childhood immunization has been practiced for over 60 years. Yet, B. pertussis remains a significant cause of morbidity in children and adults worldwide. Globally, about 20-40 million cases of pertussis are reported each year, with about 400,000 cases being fatal. The incidence of pertussis is highest and the severity the greatest in children under 6 months of age. Vaccination and natural infection are not protective for life, and the reason is unclear. The epidemiologic features of B. pertussis infections in older individuals who are only partially immune from prior infections and immunizations are not well understood. Clarification is important, in light of studies that suggest that pertussis is a cause of prolonged cough illness in adults who serve as the reservoir of B. pertussis and are the major source of infection for infants in whom the disease has substantial morbidity and mortality. With the considerable increase in cases and outbreaks, there is an imminent need for improved immunogenic and efficacious pertussis vaccines, paired with the best tools to evaluate vaccines and vaccine programs. VaxDesign has proposed two studies for acellular vaccine primed (acP) versus whole cell vaccine primed (wcP) donors, to further develop and validate a number of practical assays for use as biomarkers and to define a baseline readout for pertussis vaccinations from these two cohorts. In addition, these assays will be optimized to use the small blood volumes that are routinely available from clinical studies. In contrast to measuring humoral immune responses, the cell mediated immune response (CMI) is a substantially more challenging parameter to assess and thus the sample volumes required for the study must be large enough to allow the multiple different assessments. In this study, samples will be taken to evaluate transcriptomics, and humoral and cellular immunity over a one month period following vaccination. The collaboration with the Canadian Center for Vaccinology (CCfV) offers a unique opportunity of easily accessing acellular vaccine primed individuals.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pertussis

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Adacel®
Arm Type
Experimental
Arm Description
All participants will receive one booster dose of commercially available Adacel® (TdaP-Tetanus, diphtheria, acellular pertussis) vaccine
Intervention Type
Biological
Intervention Name(s)
Adacel®
Intervention Description
Vaccine for TdaP-Tetanus, diphtheria, acellular pertussis
Primary Outcome Measure Information:
Title
Determine best assay to evaluate CMI responses post-vaccination: CD4 T-cell proliferation
Description
% CD4+CTV-T cells analyzed by flow cytometry
Time Frame
Days -14 to 28
Title
Determine best assay to evaluate CMI responses post-vaccination: CD8 T-cell proliferation
Description
% CD8+ CTV-T cells analyzed by flow cytometry
Time Frame
Days -14 to 28
Title
Determine optimal time point for sample collection: CD4 T-cell responses
Description
% CD4+CTV-cytokine+T cells analyzed by flow cytometry
Time Frame
Days -14 to 28
Title
Determine optimal time point for sample collection: CD8 T-cell responses
Description
% CD8+ CTV-cytokine+T cells analyzed by flow cytometry
Time Frame
Days -14 to 28
Secondary Outcome Measure Information:
Title
Transcriptomic profiling of host - B. pertussis antigen interactions: B-cell plasmablasts
Description
ASC per 106 PBMCs (ELISpot)
Time Frame
Days -7, 7, 14, and 28
Title
Transcriptomic profiling of host - B. pertussis antigen interactions: B-cell plasmablasts
Description
% CD19+ CD38+ CD27+ cells
Time Frame
Days -7, 7, 14, and 28

10. Eligibility

Sex
All
Minimum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age ≥16years Primed during infancy with an acellular pertussis vaccine Good general health status, as determined by history no greater than 30 days prior to administration of the first test article Written informed consent provided If female of child-bearing potential, has a negative pregnancy test on the day of consent and has agreed to continue adequate contraception until after the last blood draw. Exclusion Criteria: Not primed in infancy with an acellular pertussis vaccine History of anemia Underlying chronic medical condition requiring ongoing monitoring by a physician (e.g., diabetes, seizure disorder) Underlying cardiac and/or pulmonary disease including hypertension, angina, prior myocardial infection, asthma, emphysema, chronic bronchitis, and pulmonary tuberculosis Pregnant (known before or established at the time of screening using a urine-based test) Immunocompromised (reporting HIV/AIDS positive or receiving immunosuppressive therapy involving steroids) Vaccinated against pertussis within previous 5 years Refusing to get an Adacel® (TdaP) vaccination dose
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Scott A Halperin, MD
Organizational Affiliation
Dalhousie
Official's Role
Principal Investigator
Facility Information:
Facility Name
Canadian Center for Vaccinology
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3K 6R8
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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Adacel® Booster Vaccination for CMI Assay Development

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