KEMRI-Wellcome Trust Research Programme (KWTRP), Centre for Geographic Medical Research - Coast (CGMRC), Kilifi, Kenya.
KEMRI-Wellcome Trust Research Programme (KWTRP), Centre for Geographic Medical Research - Coast (CGMRC), Kilifi, Kenya.
Vaccine. 2021 Aug 23;39(36):5095-5105. doi: 10.1016/j.vaccine.2021.07.033. Epub 2021 Jul 31.
BACKGROUND: Streptococcus pneumoniae is one of the most common bacterial pathogens of infants and young children. Antibody responses against the pneumococcal polysaccharide capsule are the basis of vaccine-mediated protection. We examined the relationship between the dose of polysaccharide in pneumococcal conjugate vaccines (PCVs) and immunogenicity. METHODS: A systematic search of English publications that evaluated the immunogenicity of varying doses of pneumococcal conjugate vaccines was performed in Medline and Embase (Ovid Sp) databases in August 2019. We included only articles that involved administration of pneumococcal conjugate vaccine in humans and assessed the immunogenicity of more than one serotype-specific saccharide dose. Results were synthesised descriptively due to the heterogeneity of product valency, product content and vaccine schedule. RESULTS: We identified 1691 articles after de-duplication; 9 studies met our inclusion criteria; 2 in adults, 6 in children and 1 in both. Doses of polysaccharide evaluated ranged from 0.44 mcg to 17.6 mcg. In infants, all doses tested elicited IgG geometric mean concentrations (GMCs) above the established correlate of protection (COP; 0.35 mcg/ml). A month after completion of the administered vaccine schedule, 95% confidence intervals of only three out of all the doses evaluated had GMCs that crossed below the COP. In the adult studies, all adults achieved GMCs that would be considered protective in children who have received 3 standard vaccine doses. CONCLUSION: For some products, the mean antibody concentrations induced against some pneumococcal serotypes increased with increasing doses of the polysaccharide conjugate, but for other serotypes, there were no clear dose-response relationships or the dose response curves were negative. Fractional doses of polysaccharide which contain less than is included in currently distributed formulations may be useful in the development of higher valency vaccines, or dose-sparing delivery for paediatric use.
背景:肺炎链球菌是婴幼儿最常见的细菌病原体之一。针对肺炎球菌多糖荚膜的抗体反应是疫苗介导保护的基础。我们研究了肺炎球菌结合疫苗(PCV)中多糖剂量与免疫原性之间的关系。
方法:2019 年 8 月,我们在 Medline 和 Embase(Ovid Sp)数据库中进行了系统检索,以查找评估不同剂量肺炎球菌结合疫苗免疫原性的英文文献。我们仅纳入了在人体中使用肺炎球菌结合疫苗并评估了多种血清型特异性多糖剂量免疫原性的文章。由于产品效价、产品含量和疫苗接种方案的异质性,结果仅进行描述性综合。
结果:去重后共识别出 1691 篇文章;9 项研究符合纳入标准;其中 2 项为成人研究,6 项为儿童研究,1 项为成人和儿童均有。评估的多糖剂量范围为 0.44 mcg 至 17.6 mcg。在婴儿中,所有测试剂量均产生了高于已建立的保护相关性(0.35 mcg/ml)的 IgG 几何平均浓度(GMC)。在完成接种疫苗方案一个月后,只有所有评估剂量中的三个剂量的 GMC 置信区间低于 COP。在成人研究中,所有成年人都达到了在接受 3 剂标准疫苗的儿童中被认为具有保护作用的 GMC。
结论:对于某些产品,针对某些肺炎球菌血清型诱导的平均抗体浓度随着多糖结合物剂量的增加而增加,但对于其他血清型,没有明确的剂量反应关系或剂量反应曲线为负。包含的多糖少于目前已分发制剂的多糖分数剂量可能有助于开发更高效价的疫苗,或用于儿科的剂量节约递送。
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