Impact of Bacterial Expression and Immune Response in the Severity of Pertussis
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 210
- 试验地点
- 14
- 主要终点
- Measurement of expression level of Bp genes during infection by Nanostring transcriptomic analysis of Bp isolates from the nasopharynx of children with pertussis.
研究概览
简要总结
The resurgence of pertussis is associated with an evolutionary mechanism under the pressure of current acellular vaccines, with a possible impact on vaccine effectiveness and disease expression. Little is known about the mechanisms involved in the clinical variability of pertussis, including its most severe malignant form observed in infants (mortality between 50-80%). The main challenges are: (i) the lack of knowledge about the gene expression of B. pertussis strains currently circulating during human infection, incorporating evolutionary changes and vaccine-induced selective pressure; (ii) the poor understanding of the variability in clinical expression of pertussis, and (iii) the lack of biomarkers to predict disease severity or prognosis in infants.
An integrative strategy combining a clinical, microbiological, immunological and 'omic' approach from a prospective cohort of children with pertussis will be used to identify
- 'in situ' expression profiles of B. pertussis genes and proteins incorporating recent evolutionary changes and
- a systemic and respiratory immune signature in B. pertussis-infected children according to severity.
Results should furthermore serve as a prerequisite for the identification of severity biomarkers and new vaccine antigen candidates taking into account specific immune responses in infants.
详细描述
The study design is characterized by 4 work packages:
- Collection of clinical data and biological samples (deep nasal swab, blood sample) from children with pertussis
- Construction and validation of a microbial panel of 200 genes of interest (involved in virulence and/or potential vaccine antigens) for transcriptomic analysis
- Transcriptomic study using the panel of interest of B. pertussis isolates from nasopharyngeal swabs preserved with an RNA stabilizer, using the Nanostring® technique
- Study of the immune response during pertussis
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- — 至 15 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •be between the ages of 0 and 15 years inclusive
- •be suspected of having pertussis by the physician in charge, with the prescription of a diagnostic PCR (pertussis PCR, which may be a syndromic PCR, a PCR targeting IS481 and/or IS1001)
- •be free of any pathology/treatment that may influence the immune response (autoimmune/inflammatory pathology or immune deficiency not listed above, hepatic insufficiency, taking immunosuppressive treatment (including taking oral corticosteroids with a dose ≥ 10 mg/d Prednisone equivalent for more than 15 days)
- •Have received age-appropriate information and written assent or consent from their parents/legal guardians
- •be affiliated with or benefiting from a social security plan
排除标准
- •Patient with any pathology/treatment that may influence the immune response (autoimmune/inflammatory pathology or immune deficiency not listed above, hepatic failure, taking immunosuppressive therapy (including oral corticosteroids with dose ≥ 10 mg/d prednisone equivalent for more than 15 days)
- •Use of antibiotics active against pertussis in the 24 hours preceding the sampling
- •Delay between the result of the diagnostic sample (pertussis PCR) and the day of inclusion > 48 hours
- •Patient's condition that, in the opinion of the physician, is incompatible with the expanded/additional sampling(s) required by the study
- •Infant with a weight < 2.5 kg at the time of inclusion.
结局指标
主要结局
Measurement of expression level of Bp genes during infection by Nanostring transcriptomic analysis of Bp isolates from the nasopharynx of children with pertussis.
时间窗: 3 years
To identify in a standardized way the microbial "in situ" expression profiles of currently circulating Bp genes during infection in children ;
Phenotyping of immune cells by cytometry with a 20-color flow cytometry panel
时间窗: 3 years
To determine systemic and respiratory immune responses in children during pertussis.
Measurement of plasma cytokine and chemokine concentrations by SIMOA digital ELISA
时间窗: 3 years
To determine systemic and respiratory immune responses in children during pertussis.
次要结局
- Measurement of high expression level of Bp genes in all clinical forms of pertussis by Nanostring transcriptomic analysis of Bp isolates(3 years)
- Measurement of expression level of Bp genes which is associated with severe pertussis by Nanostring transcriptomic analysis of Bp isolates(3 years)
- Measurement of expression level of Bp genes which is modified by recent gene developments related to vaccine pressure by Nanostring transcriptomic analysis of Bp isolates(3 years)