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临床试验/NCT04543669
NCT04543669已完成4 期

Adacel® (TdaP-Tetanus, Diphtheria, Acellular Pertussis) Booster Vaccination of Acellular Pertussis Vaccine-primed Individuals for Cell Mediated Immunity Assay Development

Dalhousie University2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2017年7月12日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
10
试验地点
2
主要终点
Determine best assay to evaluate CMI responses post-vaccination: CD4 T-cell proliferation

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
17 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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

结局指标

主要结局

Determine best assay to evaluate CMI responses post-vaccination: CD4 T-cell proliferation

时间窗: Days -14 to 28

% CD4+CTV-T cells analyzed by flow cytometry

Determine best assay to evaluate CMI responses post-vaccination: CD8 T-cell proliferation

时间窗: Days -14 to 28

% CD8+ CTV-T cells analyzed by flow cytometry

Determine optimal time point for sample collection: CD4 T-cell responses

时间窗: Days -14 to 28

% CD4+CTV-cytokine+T cells analyzed by flow cytometry

Determine optimal time point for sample collection: CD8 T-cell responses

时间窗: Days -14 to 28

% CD8+ CTV-cytokine+T cells analyzed by flow cytometry

次要结局

  • Transcriptomic profiling of host - B. pertussis antigen interactions: B-cell plasmablasts(Days -7, 7, 14, and 28)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Scott Halperin

Professor and Director, Canadian Centre for Vaccinology

Dalhousie University

研究点 (2)

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