Huffman Anthony, Ong Edison, Brunson Tim, Sanati Nasim, Zheng Jie, Masci Anna Maria, Wu Guanming, He Yongqun
Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, United States.
Oregon Health & Science University, Portland, Oregon, OR, United States.
CEUR Workshop Proc. 2023 Aug-Sep;3603:1-12.
ImmPort, the world's largest repository of immunology data, includes many vaccine immune response datasets. ImmPort maps the metadata of these studies to ontology and database schema. As of February 28, 2023, our ImmPort data analysis identified 6.258 immune exposures using 47 vaccines in 4,607 human subjects, and 324 cohort studies from the ImmPort. We hypothesized that an integrative ontological representation of the data from these studies would enhance our understanding and analysis of these ImmPort vaccine studies, and with ontological classification and tools such as VIGET, we could further study the effects of different conditions such as vaccine types and host biological sex on the vaccine response gene expression profiles. Our Vaccine Ontology (VO) analysis classified these 37 vaccines into bacterial, viral, and protozoan vaccine types with different vaccine properties. The ImmPort metadata types were modeled with the Vaccine Investigation Ontology (VIO). Our new ontology-based pipeline extracted vaccine response data from the ImmPort database, annotated them based on ontology, obtained corresponding gene expression data from the GEO, and performed consistent omics data analysis. Our use case found gene profiles shared and differed from live and killed inactivated influenza vaccines. Furthermore, our Omics data analysis using the VIGET tool found that female and male human subjects have differential host responses for influenza vaccines. For example, our study showed much stronger early female responses to influenza vaccination than males, and males was able to show active immune responses at a later stage. Interestingly, the female (but not male) human subject group also showed significantly enriched neutrophil degranulation at Day 3 after influenza vaccination; however, males (but not females) displayed significantly enriched neutrophil degranulation at Day 14 after influenza vaccination. These mechanisms have been used to find differences between the gene lists and pathways of host responses to different vaccines conditional to different factors including vaccine types and host biological sex. Moreover, this framework can be expanded to other vaccines and vaccine categories easily.
ImmPort是世界上最大的免疫学数据储存库,包含许多疫苗免疫反应数据集。ImmPort将这些研究的元数据映射到本体和数据库模式。截至2023年2月28日,我们的ImmPort数据分析在4607名人类受试者中使用47种疫苗识别出6258次免疫暴露,以及来自ImmPort的324项队列研究。我们假设对这些研究数据进行综合本体表示将增强我们对这些ImmPort疫苗研究的理解和分析,并且借助本体分类和诸如VIGET之类的工具,我们可以进一步研究不同条件(如疫苗类型和宿主生物学性别)对疫苗反应基因表达谱的影响。我们的疫苗本体(VO)分析将这37种疫苗分为具有不同疫苗特性的细菌、病毒和原生动物疫苗类型。ImmPort元数据类型使用疫苗研究本体(VIO)进行建模。我们基于本体的新流程从ImmPort数据库中提取疫苗反应数据,基于本体对其进行注释,从GEO获取相应的基因表达数据,并进行一致的组学数据分析。我们的用例发现了活流感疫苗和灭活流感疫苗共有的和不同的基因谱。此外,我们使用VIGET工具进行的组学数据分析发现,女性和男性人类受试者对流感疫苗的宿主反应存在差异。例如,我们的研究表明,女性对流感疫苗的早期反应比男性强得多,而男性能够在后期表现出活跃的免疫反应。有趣的是,女性(而非男性)人类受试者组在流感疫苗接种后第3天也显示出明显富集的中性粒细胞脱颗粒;然而,男性(而非女性)在流感疫苗接种后第14天显示出明显富集的中性粒细胞脱颗粒。这些机制已被用于发现宿主对不同疫苗的反应在不同因素(包括疫苗类型和宿主生物学性别)条件下基因列表和途径之间的差异。此外,该框架可以轻松扩展到其他疫苗和疫苗类别。