Suppr超能文献

在冈比亚进行的一项疗效试验中确定的9价肺炎球菌结合疫苗(PCV-9)的免疫原性和血清型特异性疗效。

Immunogenicity and serotype-specific efficacy of a 9-valent pneumococcal conjugate vaccine (PCV-9) determined during an efficacy trial in The Gambia.

作者信息

Saaka M, Okoko B J, Kohberger R C, Jaffar S, Enwere G, Biney E E, Oluwalana C, Vaughan A, Zaman S M A, Asthon L, Goldblatt D, Greenwood B M, Cutts F T, Adegbola R A

机构信息

Medical Research Council Laboratories, Fajara, Banjul, Gambia.

出版信息

Vaccine. 2008 Jul 4;26(29-30):3719-26. doi: 10.1016/j.vaccine.2008.04.066. Epub 2008 May 16.

Abstract

This study aimed to determine the immunogenicity of a 9-valent pneumococcal conjugate vaccine (PCV-9) in a subgroup of Gambian children enrolled in a large vaccine efficacy trial. To place the antibody results in context, in this paper we also report previously unpublished data on serotype-specific clinical vaccine efficacy from the main trial. In the sub-study, a single 2-4 ml venous blood specimen was collected from 212 Gambian children 4-6 weeks after the administration of a third dose of PCV-9 or placebo. IgG antibodies to pneumococcal serotype 1, 4, 5, 6B, 9V, 14, 18C, 19F and 23F polysaccharides were measured by ELISA. The proportions of infants with antibody concentrations above 0.2, 0.35 and 1.0 microg/ml, and the geometric mean concentrations (GMCs) of anti-pneumococcal polysaccharide antibodies were substantially higher for each serotype in children who received three doses of PCV-9 than those in the placebo group. Among PCV-9 recipients, GMCs ranged between 2.61 and 11.09 microg/ml with the highest being against serotype 14 and the lowest against 9V polysaccharide. The estimated overall protective antibody level for all nine serotypes, based on the vaccine efficacy against vaccine-type invasive pneumococcal disease (IPD) of 77% (95% CI: 51, 90) observed in the trial, was 2.3 microg/ml (95% CI: 1.0, 5.0). The PCV-9 studied was immunogenic in a Gambian population where it was also found to be efficacious.

摘要

本研究旨在确定9价肺炎球菌结合疫苗(PCV-9)在参与一项大型疫苗效力试验的冈比亚儿童亚组中的免疫原性。为了全面呈现抗体结果,在本文中我们还报告了该主要试验中以前未发表的血清型特异性临床疫苗效力数据。在这项子研究中,在给212名冈比亚儿童接种第三剂PCV-9或安慰剂4至6周后,采集了一份2 - 4毫升的静脉血标本。通过酶联免疫吸附测定法(ELISA)检测了针对肺炎球菌血清型1、4、5、6B、9V、14、18C、19F和23F多糖 的IgG抗体。在接受三剂PCV-9的儿童中,每种血清型抗体浓度高于0.2、0.35和1.0微克/毫升的婴儿比例以及抗肺炎球菌多糖抗体的几何平均浓度(GMCs)均显著高于安慰剂组。在PCV-9接种者中,GMCs在2.61至11.09微克/毫升之间,最高的是针对血清型14,最低的是针对9V多糖。根据试验中观察到的针对疫苗型侵袭性肺炎球菌疾病(IPD)77%(95%CI:51,90)的疫苗效力,所有九种血清型的估计总体保护性抗体水平为2.3微克/毫升(95%CI:1.0,5.0)。所研究的PCV-9在冈比亚人群中具有免疫原性,且在该人群中也被发现具有效力。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验