Pertussis Immunization Programs in Low Income Countries
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 3,587
- 试验地点
- 3
- 主要终点
- Proportion of biologically confirmed cases of pertussis in patients under 6 months old admitted into hospital with clinical signs corresponding to whooping cough syndrome.
研究概览
简要总结
Due to waning of infectious as well as vaccine immunity and lack of vaccination boosters, a large number of adolescents and adults are no longer immunized against Bordetella pertussis, the agent of whooping cough and consequently may contract whooping cough. Furthermore, these populations represent a reservoir of the infectious agent from which the dissemination to non-immune infants is possible, causing severe illness, or even death, in this age group.
Few studies have been carried out on whooping cough in developing countries (incidence, contaminator's age, etc.) and, specifically, none have assessed the duration of protection induced by the whole cell pertussis (wP) vaccine mainly presently used in these countries.
However, data on the duration of vaccine induced protection are essential to determine i) the usefulness of vaccine boosters and ii) the target age group for these boosters.
The aims of the present study are:
- To evaluate the proportion of confirmed pertussis cases in infants presenting whooping cough syndrome (WP1a)
- To evaluate the proportion of confirmed pertussis cases or healthy carriers among contact cases
- To determine origin of the infant's contamination (WP1b)
- To determine the duration of protection induced by the wP vaccines used in contact cases and the child population aged 3 to 15 yo (WP1b and WP2)
- To bring new scientific evidences documenting the potential need for initiating boosters (WP1b and WP2)
- To allow a comparison of the results with those obtained using the same methodology for the acellular pertussis vaccine and/or in other contexts. Potential implications for the use of pertussis vaccines in low and moderate income countries.
- To increase local capabilities by the transfer of materials and expertise that will make the diagnosis of pertussis possible in the centres of reference and strengthen a pertussis monitoring network in the implicated countries.
- To improve children's health through a better match of the vaccination schedule according to the reality of the situation.
详细描述
Background:
Vaccination of infants and young children with a whole-cell pertussis (wP) vaccine dramatically decreased the mortality and morbidity due to B. pertussis. However, twenty-five years of "honeymoon" period, after the introduction of high vaccination coverage, reappearance of whooping cough cases in industrialized countries was observed in infants contaminated by adolescents and adults. This modification in transmission of the disease after the introduction of the wP vaccine indicated that the immunity provided by the vaccine is not lifelong, just like that provided by natural infection, and that it decreases7-9 years after the first vaccination and the first booster. Due to secondary effects, wP vaccines cannot be used for boosters. Moreover, the wP vaccines have been shown to be different in terms of efficacy (varying from 30 to 95%). Acellular pertussis (aP) vaccines consisting of purified and inactivated bacterial proteins, have therefore been developed and commercialized. These vaccines induce much fewer side effects and may therefore be used for primary-vaccination as well as for vaccine boosters. They are expensive but have more reproducible manufacturing. The humoral and long-term cell-mediated immunities granted by the aP vaccines have been shown to be comparable to the immunity granted by the wP vaccines, effective for 6-7 years after the booster vaccine in the second year of life, also inducing different cell immunity. Since 2007, the proportion of B. pertussis and B. parapertussis isolates no longer producing vaccine antigen(s) has increased in the industrialized countries that use aP vaccines. These isolates may decrease the efficacy of the aP vaccines. Does this type of isolates circulate in the Low income countries still using wP vaccines ? Does it reduce the efficacy of the wP vaccines? Moreover, the wP vaccines used in the Southern countries have not been assessed like the ones used in the Northern countries. In particular, the duration of protection after the primary-vaccination and a vaccine booster is not known.
Rational:
For various reasons, a large difference exits between the monitoring systems across the world: awareness of the disease is variable depending on the population; differences in the immunization coverage and strategies; diverse compositions of the vaccines used; but overall the large differences between the vaccines in terms of immunity against the disease, protection against infection and/or decrease in the transmission of the pathogen. The underestimation of pertussis is recognized by the World Health Organisation (WHO) and the (Global Pertussis Initiative) who highlight the problem of the reliability of the declared data.
This situation is the result of i) limited use of biological diagnostics (problems in isolating the bacteria in the laboratories); ii) diagnostic errors due to the fact that diagnosis is mainly clinical ; iii) inadequate monitoring of the illness ; iv) a lack of awareness among physicians. Pertussis is not considered when it is comes to identifying the respiratory pathogen: most clinicians continue to consider it as only a child illness and ignore adult infections. The absence of an available tool allowing a reliable diagnostic to be made makes difficult to assess the real impact of this pathogen in child respiratory syndromes.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Cohort 1 (WP1a)
- •Infants under 6 months old
- •Presenting clinical signs of a whooping cough syndrome
- •Written consent obtained from a parent/guardian of the child
- •Cohort 2 (WP1b)
- •People in regular and prolonged contact (>1h per day) with the index case for at least 5 days before the signs of whooping cough occurred in the infected child, living (or not) in the same household.
- •For the adults, written consent obtained.
- •For minors under 7 yo: written consent obtained from a parent/guardian.
- •For minors over 7 yo: written consent obtained from parent/guardian and oral assent obtained from the child.
- •Cohort 3 (WP2)
- •Child aged between 3 and 15 yo
- •Up to date first pertussis vaccination (vaccination booklet or official register)
- •Last pertussis vaccination done more than one year before inclusion
- •For minors under 7 yo: written consent obtained from parent/guardian.
- •For minors over 7 yo: written consent obtained from parent/guardian and oral assent obtained from the child.
排除标准
- •Cohort 3 (WP2)
- •Pertussis vaccination done more than one year before inclusion
结局指标
主要结局
Proportion of biologically confirmed cases of pertussis in patients under 6 months old admitted into hospital with clinical signs corresponding to whooping cough syndrome.
时间窗: November 2018
Primary Outcome of WP1a (Cohort 1)
Proportion of cases tested positive for B.Pertussis given by the presence of B. pertussis DNA in the nasopharyngeal sample or by the presence of an anti-pertussis toxin IgG level >100 IU/mL in the serum.
时间窗: November 2018
Primary Outcome of WP1b (Cohort 2)
Proportion of cases tested positive given by the presence of an anti-pertussis toxin IgG level >100 IU/mL in the serum.
时间窗: November 2018
Primary Outcome of WP2 (Cohort 3)
次要结局
- Estimation of the relative risk of the disease occurring in the contact patients based on their immunization status and age groups(April 2019)
