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A conjugate vaccine against typhoid fever

机译:抗伤寒的复合疫苗

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Zulfiqar Bhutta and colleages' study in The Lancet Infectious Diseases marks an important milestone for the use of typhoid conjugate vaccines. Present Vi polysaccharide vaccines (Vi-PS) are not widely used because they cannot be given to children younger than 2 years and are thus excluded frorh the Expanded Programme of Immunization (EPI); furthermore, their effectiveness decreases rapidly after 2-3 years. Expectations of a typhoid conjugate vaccine include safe administration to children younger than 2 years, the induction of protective IgG anti-Vi immune responses, and the development of long-term, and at best lifelong, protection. Such an improved vaccine against typhoid fever could have substantial global effect in endemic regions. Bhutta and colleagues present data from their two phase 2 clinical trials of the immunogenicity and safety of conjugate typhoid vaccine Vi-CRM~197. The findings show that the vaccine was safe when given to children younger than 2 years of age, rendering it a suitable candidate for inclusion into EPI programmes. Significant post-vaccination antibody titre concentrations, although largely similar to those of the Vi-PS, were reported.
机译:Zulfiqar Bhutta及其同事在《柳叶刀传染病》中的研究标志着使用伤寒结合疫苗的重要里程碑。目前的Vi多糖疫苗(Vi-PS)不能被广泛使用,因为它们不能提供给2岁以下的儿童,因此被扩展免疫计划(EPI)排除在外;此外,它们的效果在2-3年后迅速下降。伤寒共轭疫苗的期望包括对2岁以下的儿童安全给药,诱导保护性IgG抗Vi免疫反应以及发展长期(最好是终生)保护。这种针对伤寒的改良疫苗可能会在地方性流行地区产生重大全球影响。 Bhutta及其同事提供了两项关于结合伤寒疫苗Vi-CRM〜197的免疫原性和安全性的2期临床试验数据。研究结果表明,将疫苗接种到2岁以下的儿童中是安全的,使其成为加入EPI计划的合适人选。尽管与Vi-PS的抗体效价浓度基本相似,但仍报告了明显的疫苗后效价浓度。

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