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Baseline Serum Vitamin A and D Levels Determine Benefit of Oral Vitamin AD Supplements to Humoral Immune Responses Following Pediatric Influenza Vaccination

机译:基线血清维生素A和D水平决定口服维生素A&D补充剂对儿科流感疫苗接种后的体液免疫应答的益处

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摘要

Maximizing vaccine efficacy is critical, but previous research has failed to provide a one-size-fits-all solution. Although vitamin A and vitamin D supplementation studies have been designed to improve vaccine efficacy, experimental results have been inconclusive. Information is urgently needed to explain study discrepancies and to provide guidance for the future use of vitamin supplements at the time of vaccination. We conducted a randomized, blinded, placebo-controlled study of influenza virus vaccination and vitamin supplementation among 2 to 8 (inclusive) year old children over three seasons, including 2015−2016 (n = 9), 2016−2017 (n = 44), and 2017−2018 (n = 26). Baseline measurements of vitamins A and D were obtained from all participants. Measurements were of serum retinol, retinol-binding protein (RBP, a surrogate for retinol), and 25-hydroxyvitamin D (25(OH)D). Participants were stratified into two groups based on high and low incoming levels of RBP. Children received two doses of the seasonal influenza virus vaccine on days 0 and 28, either with an oral vitamin supplement (termed A&D; 20,000 IU retinyl palmitate and 2000 IU cholecalciferol) or a matched placebo. Hemagglutination inhibition (HAI) antibody responses were evaluated toward all four components of the influenza virus vaccines on days 0, 28, and 56. Our primary data were from season 2016−2017, as enrollment was highest in this season and all children exhibited homogeneous and negative HAI responses toward the Phuket vaccine at study entry. Responses among children who entered the study with insufficient or deficient levels of RBP and 25(OH)D benefited from the A&D supplement (p < 0.001 for the day 28 Phuket response), whereas responses among children with replete levels of RBP and 25(OH)D at baseline were unaffected or weakened (p = 0.02 for the day 28 Phuket response). High baseline RBP levels associated with high HAI titers, particularly for children in the placebo group (baseline RBP correlated positively with Phuket HAI titers on day 28, r = 0.6, p = 0.003). In contrast, high baseline 25(OH)D levels associated with weak HAI titers, particularly for children in the A&D group (baseline 25(OH)D correlated negatively with Phuket HAI titers on day 28, r = −0.5, p = 0.02). Overall, our study demonstrates that vitamin A&D supplementation can improve immune responses to vaccines when children are vitamin A and D-insufficient at baseline. Results provide guidance for the appropriate use of vitamins A and D in future clinical vaccine studies.
机译:最大限度地提高疫苗效力是至关重要的,但以往的研究未能提供一个放之四海而皆准的解决办法。虽然维生素A和维生素d补充研究的目的是为了提高疫苗的有效性,实验结果尚无定论。信息是目前急需研究解释不符,并在接种疫苗时的将来使用的维生素补充剂提供指导。我们在三个赛季中进行了一项随机,双盲,安慰剂对照的流感病毒疫苗接种和补充维生素的研究中2到8(含)岁的儿童,其中包括2015 - 2016年(N = 9),2016-2017(N = 44) ,和2017年至2018年(N = 26)。从所有参与者获得维生素A和维生素d的基线测量。测量是血清视黄醇,视黄醇结合蛋白(RBP,视黄醇的替代物),和25-羟基d(25(OH)d)的。参与者基于RBP的高和低传入水平分层分为两组。儿童接受第0天及28两个剂量的季节性流感病毒疫苗的,无论是与口服维生素补充(称为A&d; 20000 IU维生素A棕榈酸酯和2000 IU胆钙化醇)或匹配的安慰剂。血凝抑制(HAI)抗体应答朝向流感病毒疫苗的所有四个组件评价第0天,28和56。我们的主要数据来自2016 - 2017年的季节,如登记在这个季节最高和所有儿童表现出均匀的和对在研究项目普吉疫苗负HAI响应。谁与水平不足或缺乏的RBP和25(OH)d的从A&d补充受益(P <0.001的第28天布吉响应)进入研究,而响应与RBP和25(的充满水平的儿童中的儿童中的响应OH在基线)d不受影响或减弱(p值= 0.02为天28布吉响应)。具有高滴度HAI相关联,特别是用于在安慰剂组中的儿童高基线RBP水平(基线RBP与在第28天布吉HAI滴度,R = 0.6,p值= 0.003正相关)。相反,用弱HAI滴度相关的高基线25(OH)d的水平,特别是对于A&d组的儿童(基线25(OH)d与布吉HAI滴度在第28天呈负相关,R = -0.5,P = 0.02) 。总的来说,我们的研究表明,维生素A&d补充可以提高疫苗的免疫反应,当孩子是维生素A和基线d-不足。结果为今后的临床疫苗研究的正确使用维生素A和维生素d的指导。

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