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首页> 外文期刊>Vaccine >Comparison of anti-capsular antibody quantity and functionality in children after different primary dose and booster schedules of 13 valent-pneumococcal conjugate vaccine
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Comparison of anti-capsular antibody quantity and functionality in children after different primary dose and booster schedules of 13 valent-pneumococcal conjugate vaccine

机译:不同初级剂量和13例肺炎球菌缀合物疫苗后儿童抗囊抗体抗体量和功能的比较

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摘要

Different schedules for pediatric use of the 13-valent pneumococcal conjugate vaccine (PCV-13) are recommended in different countries and the U.S. Advisory Committee on Immunization Practices (ACIP) has considered potential of changing from 3 primary doses plus a booster (3p + 1) to two primary doses plus a booster (2p + 1) for protection against Streptococcus pneumoniae. In this paper, we report results of IgG antibody measured by ELISA and opsonophagocytic assay (OPA) after 2p, 3p, at child age 15 months of pre-booster and 18 months (post-booster) in serum samples opportunistically available from a prior study that focused on PCV effectiveness against AOM. A total of similar to 100 sera for each of the 4 study time points (390 sera tested) from 169 children were tested. Geometric mean concentrations (GMCs) and percentage of children exceeding the presumed protective antibody thresholds measured by ELISA and OPA were calculated. 2p doses produced lower antibody levels measured by ELISA but not OPA until the booster dose for serotypes 6A, 6B, 5 and 23F only. Booster dosing at 15 months resulted in significant increases in antibody. There was no difference in the percentage of children with >= correlate of protection (COP) for OPA for 2p vs 3p doses except for serotype 23F. A 2p + 0 or 3p + 0 schedule would likely result in many children failing to sustain protective levels of antibody into the second year of life. We conclude that protection from invasive pneumococcal infection in early childhood would be similar for most serotypes in PCV13 using a 2p + 1 or 3p + 1 but not a 2p + 0 or 3p + 0 schedule. (C) 2020 Elsevier Ltd. All rights reserved.
机译:在不同的国家建议使用不同的儿科使用时间表(PCV-13),在不同的国家,美国免疫惯例(ACIP)的咨询委员会认为从3个主要剂量加助推器改变的可能性(3P + 1 )两种主要剂量加上增压器(2p + 1),用于防止链球菌肺炎料。在本文中,我们报告了ELISA和OPA)在血清预增强剂和18个月(Booster)的儿童年龄15个月内2p,3p,18个月(Booster)的IgG抗体的结果,从事事先研究重点关注对AOM的PCV效力。测试了来自169名儿童的4个研究时间点(390次测试的390次测试中的每种血清相似。计算几何平均浓度(GMCs)和超过由ELISA和OPA测量的假定保护抗体阈值的儿童的百分比。 2P剂量产生通过ELISA测量的抗体水平,但直到仅用于血清型6a,6b,5和23f的增强剂量。在15个月内加强给药导致抗体的显着增加。除血清型23F外,患儿的患儿百分比没有> = POP的百分比对2P VS 3P剂量的百分比没有差异。 2P + 0或3P + 0安排可能导致许多儿童未能维持抗体的保护水平进入生命的第二年。我们得出结论,在幼儿早期侵袭性肺炎球菌感染的保护将在PCV13中的大多数血清型使用2P + 1或3P + 1但不是2P + 0或3P + 0安排类似于PCV13中的大多数血清型。 (c)2020 elestvier有限公司保留所有权利。

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