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首页> 外文期刊>Vaccine >Pneumococcal polysaccharide 23-valent vaccine: long-term persistence of circulating antibody and immunogenicity and safety after revaccination in adults.
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Pneumococcal polysaccharide 23-valent vaccine: long-term persistence of circulating antibody and immunogenicity and safety after revaccination in adults.

机译:肺炎球菌多糖23价疫苗:成人免疫后长期循环抗体的持久性以及免疫原性和安全性。

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摘要

Since publication of a 1997 review of the immunogenicity and safety data for pneumococcal polysaccharide vaccines (PPSVs), dozens of additional studies have been published, involving larger cohorts, longer observation periods, and more specific assays. Additionally, a 13-valent pneumococcal conjugate vaccine (PCV) has been licensed for adults. This paper reviews adult studies assessing antibody persistence for 鈮? years after pneumococcal vaccination, and adult studies of immunogenicity and safety after revaccination. This review emphasizes the currently registered PPSV23 formulations containing 25-g polysaccharide per serotype, for which far more long-term data are available. Broadly, IgG and functional antibody levels after PPSV23 in adults persist above concentrations in unvaccinated adults for at least 5-10 years in most studies. The few exceptions involve populations of non-ambulatory adults or those with confounding host-factor issues. Revaccination with PPSV23 5-10 years after a previous dose consistently and substantially increases both IgG and functional antibody levels. There is an inverse association between circulating antibody level just before primary or revaccination and subsequent antibody increase. Although injection-site reactions (e.g., pain, swelling, redness) were reported more commonly after PPSV23 revaccination than after primary vaccination in most studies, these reactions typically resolved within 5 days. We interpret the contemporary literature as supporting pneumococcal revaccination as a means to sustain anti-pneumococcal antibodies at levels greater than among unvaccinated adults. PPSV23 is a broad-spectrum public-health tool to help prevent serious pneumococcal diseases across the adult lifespan.
机译:自1997年发表关于肺炎球菌多糖疫苗(PPSV)的免疫原性和安全性数据的综述以来,已经发表了许多其他研究,涉及更大的队列,更长的观察期和更具体的测定方法。此外,一种13价肺炎球菌结合疫苗(PCV)已获准用于成人。本文综述了评估抗体持久性≤?的成人研究。肺炎球菌疫苗接种后数年,以及成年后免疫原性和安全性研究。这篇综述着重介绍了目前注册的每血清型含25 g多糖的PPSV23制剂,可得到更多的长期数据。广泛地说,在大多数研究中,成年人PPSV23之后的IgG和功能性抗体水平持续高于未接种疫苗的成年人至少5-10年。少数例外情况涉及非流动成年人或具有混杂宿主因素问题的成年人。在先前剂量后5-10年用PPSV23再次接种疫苗,可以持续且实质上增加IgG和功能性抗体水平。在初次或再次免疫之前,循环抗体水平与随后的抗体升高之间存在负相关关系。尽管在大多数研究中,PPSV23疫苗接种后报告的注射部位反应(例如疼痛,肿胀,发红)比初次疫苗接种更为常见,但这些反应通常在5天内消失。我们将当代文献解释为支持肺炎球菌再接种,将其作为维持抗肺炎球菌抗体水平高于未接种疫苗的成年人的一种手段。 PPSV23是一种广谱的公共卫生工具,可帮助预防成年人整个寿命期间的严重肺炎球菌疾病。

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