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不同剂次肺炎球菌结合疫苗免疫程序诱导的记忆 B 细胞应答:越南随机对照试验分析。

Memory B cell responses induced by pneumococcal conjugate vaccine schedules with fewer doses: analysis of a randomised-controlled trial in Viet Nam.

机构信息

Infection, Immunity & Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.

Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.

出版信息

Nat Commun. 2024 Aug 14;15(1):6968. doi: 10.1038/s41467-024-51413-7.

DOI:10.1038/s41467-024-51413-7
PMID:39138203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11322157/
Abstract

The use of pneumococcal conjugate vaccine (PCV) schedules with fewer doses are being considered to reduce costs and improve access, particularly in low- and middle-income countries. While several studies have assessed their immunogenicity, there are limited data on their potential for long-term immune protection, as assessed by pneumococcal serotype-specific memory B cell (B) responses. This current study reports secondary outcome data that aims to compare B responses following reduced-dose (0 + 1 and 1 + 1) schedules of PCV10 and PCV13 in Vietnamese infants from our randomised-controlled trial (trial registration number NCT03098628). Following vaccination at 12 months of age, B levels for most serotypes peaked seven days post-vaccination and were higher in magnitude for the 1 + 1 than 0 + 1 schedules and for PCV13 than PCV10. Furthermore, B did not wane as rapidly as IgG levels by 24 months of age. Further studies are needed to assess the use of B as markers of long-term protection against pneumococcal carriage and disease, which is crucial to generate data for immunisation program decision-making.

摘要

使用剂量较少的肺炎球菌结合疫苗(PCV)方案正被考虑用于降低成本和改善可及性,特别是在低收入和中等收入国家。虽然有几项研究评估了其免疫原性,但关于其通过肺炎球菌血清型特异性记忆 B 细胞(B)反应产生长期免疫保护的潜力的数据有限。本研究报告了次要结果数据,旨在比较我们的随机对照试验(试验注册号 NCT03098628)中越南婴儿接受 PCV10 和 PCV13 减毒(0+1 和 1+1)方案后的 B 反应。在 12 个月大时接种疫苗后,大多数血清型的 B 水平在接种后 7 天达到峰值,1+1 方案比 0+1 方案和 PCV13 比 PCV10 的幅度更高。此外,到 24 个月大时,B 不像 IgG 水平那样迅速下降。需要进一步研究来评估 B 作为预防肺炎球菌定植和疾病的长期保护的标志物的使用,这对于为免疫规划决策生成数据至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebcf/11322157/5b4bbf31fe94/41467_2024_51413_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebcf/11322157/58b720110137/41467_2024_51413_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebcf/11322157/c73515f1fc7c/41467_2024_51413_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebcf/11322157/eec81563421f/41467_2024_51413_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebcf/11322157/5b4bbf31fe94/41467_2024_51413_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebcf/11322157/58b720110137/41467_2024_51413_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebcf/11322157/c73515f1fc7c/41467_2024_51413_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebcf/11322157/eec81563421f/41467_2024_51413_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebcf/11322157/5b4bbf31fe94/41467_2024_51413_Fig4_HTML.jpg

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