...
首页> 外文期刊>Journal of Translational Medicine >Development of an objective gene expression panel as an alternative to self-reported symptom scores in human influenza challenge trials
【24h】

Development of an objective gene expression panel as an alternative to self-reported symptom scores in human influenza challenge trials

机译:客观基因表达面板的开发,作为人类流感挑战试验中自我报告症状评分的替代方法

获取原文

摘要

Background Influenza challenge trials are important for vaccine efficacy testing. Currently, disease severity is determined by self-reported scores to a list of symptoms which can be highly subjective. A more objective measure would allow for improved data analysis. Methods Twenty-one volunteers participated in an influenza challenge trial. We calculated the daily sum of scores (DSS) for a list of 16 influenza symptoms. Whole blood collected at baseline and 24, 48, 72 and 96?h post challenge was profiled on Illumina HT12v4 microarrays. Changes in gene expression most strongly correlated with DSS were selected to train a Random Forest model and tested on two independent test sets consisting of 41 individuals profiled on a different microarray platform and 33 volunteers assayed by qRT-PCR. Results 1456 probes are significantly associated with DSS at 1% false discovery rate. We selected 19 genes with the largest fold change to train a random forest model. We observed good concordance between predicted and actual scores in the first test set (r?=?0.57; RMSE?=??16.1%) with the greatest agreement achieved on samples collected approximately 72?h post challenge. Therefore, we assayed samples collected at baseline and 72?h post challenge in the second test set by qRT-PCR and observed good concordance (r?=?0.81; RMSE?=??36.1%). Conclusions We developed a 19-gene qRT-PCR panel to predict DSS, validated on two independent datasets. A transcriptomics based panel could provide a more objective measure of symptom scoring in future influenza challenge studies. Trial registration Samples were obtained from a clinical trial with the ClinicalTrials.gov Identifier: NCT02014870, first registered on December 5, 2013
机译:背景流感挑战试验对于疫苗功效测试很重要。目前,疾病严重程度是由自我报告得分决定的,这些得分可能是高度主观的症状。更加客观的措施将可以改善数据分析。方法21名志愿者参加了流感挑战试验。我们计算了16种流感症状的每日总得分(DSS)。在Illumina HT12v4微阵列上分析在基线以及攻击后24、48、72和96小时收集的全血。选择与DSS最密切相关的基因表达变化来训练随机森林模型,并在两个独立的测试集上进行测试,该测试集由41位在不同微阵列平台上进行分析的个体和33位通过qRT-PCR分析的志愿者组成。结果1456个探针以1%的错误发现率与DSS显着相关。我们选择了19个倍数变化最大的基因来训练随机森林模型。我们在第一个测试集中观察到的预测分数与实际分数之间具有很好的一致性(r = 0.57; RMSE = 16.1%),并且在挑战后约72 h收集的样本达到了最大的一致性。因此,我们通过qRT-PCR分析了在第二个测试组中在基线和攻击后72小时收集的样品,并观察到良好的一致性(r = 0.81; RMSE = 36.1%)。结论我们开发了一个19基因qRT-PCR面板来预测DSS,并在两个独立的数据集上进行了验证。基于转录组学的小组可以在未来的流感挑战研究中提供更客观的症状评分方法。试验注册样本是使用ClinicalTrials.gov标识符从临床试验获得的:NCT02014870,首次注册时间为2013年12月5日

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号