Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3052, Australia.
Department of Medical Biology, University of Melbourne, Parkville, VIC 3010, Australia.
Nutrients. 2021 Oct 7;13(10):3516. doi: 10.3390/nu13103516.
Preventive zinc supplementation provided as a stand-alone dispersible tablet, or via home fortification as multiple micronutrient powders (MNPs), has been considered a potential strategy to prevent zinc deficiency and improve health (including immune) outcomes among children in low- and middle-income countries. However, the impact of zinc supplementation on immune profiles has not been well characterized. We sought to define the effect of zinc supplementation on peripheral blood gene expression and cytokine levels among young children in Dhaka, Bangladesh. In a sub-study of a large randomized, controlled, community-based efficacy trial where children 9-11 months of age received one of the following interventions on a daily basis for 24 weeks: (1) MNPs containing 10 mg of zinc; (2) dispersible tablet containing 10 mg zinc; or (3) placebo powder, we used RNA sequencing to profile the peripheral blood gene expression, as well as highly sensitive multiplex assays to detect cytokine profiles. We profiled samples from 100 children enrolled in the parent trial (zinc MNPs 28, zinc tablets 39, placebo 33). We did not detect an effect from either zinc intervention on differential peripheral blood gene expression at the end of the intervention, or an effect from the intervention on changes in gene expression from baseline. We also did not detect an effect from either intervention on cytokine concentrations. Exploratory analysis did not identify an association between undernutrition (defined as stunting, underweight or wasting) and peripheral blood gene expression. Zinc interventions in children did not produce a gene expression or cytokine signature in the peripheral blood. However, this study demonstrates a proof of principle that sensitive multi-omic techniques can be applied to samples collected in field studies.
预防性补锌以独立的可分散片剂形式提供,或通过家庭强化作为多种微量营养素粉末(MNP)提供,一直被认为是预防发展中国家儿童缺锌和改善健康(包括免疫)结局的潜在策略。然而,锌补充对免疫谱的影响尚未得到很好的描述。我们旨在确定锌补充对孟加拉国达卡的幼儿外周血基因表达和细胞因子水平的影响。在一项大型随机、对照、以社区为基础的疗效试验的子研究中,9-11 个月大的儿童每天接受以下干预措施之一,持续 24 周:(1)含 10 毫克锌的 MNP;(2)含 10 毫克锌的可分散片剂;或(3)安慰剂粉末,我们使用 RNA 测序来分析外周血基因表达,并使用高灵敏度的多重分析来检测细胞因子谱。我们对参加母试验的 100 名儿童的样本进行了分析(锌 MNP28、锌片剂 39、安慰剂 33)。我们没有发现两种锌干预措施在干预结束时对外周血差异基因表达有影响,也没有发现干预措施对从基线开始的基因表达变化有影响。我们也没有发现两种干预措施对细胞因子浓度有影响。探索性分析并未发现营养不良(定义为发育迟缓、体重不足或消瘦)与外周血基因表达之间存在关联。儿童锌干预措施在外周血中未产生基因表达或细胞因子特征。然而,这项研究证明了敏感的多组学技术可以应用于现场研究中收集的样本。