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Developing computational models to predict the immune response to B. pertussis booster vaccination

开发计算模型来预测百日咳博德特氏菌加强疫苗接种的免疫反应

基本信息

批准号：
10570832
负责人：
Bjoern Peters
金额：
$ 135.01万
依托单位：
LA JOLLA INSTITUTE FOR IMMUNOLOGY
依托单位国家：
美国
项目类别：
财政年份：
2020
资助国家：
美国
起止时间：
2020-03-10 至 2025-02-28
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10570832
关键词：
Address Adult Age Antibodies Antigen-Antibody Complex Antigens B-Lymphocytes Bacteria Biological Assay Bordetella pertussis CCL3 gene Case Study Cell Communication Cell surface Cells Child Code Communities Computer Models Country Coupled Data Demographic Impact Development Educational workshop Eligibility Determination Epidemiology Evaluation Event Feedback Fine needle aspiration biopsy Frequencies Gene Expression Gene Expression Profile Generations Grant IgG4 Immune Immune response Immune system Immunity Individual Infant Infection Measurement Measures Modeling Morbidity - disease rate Outcome Peripheral Blood Mononuclear Cell Pertussis Pertussis Vaccine Phenotype Plasma Process Protocols documentation Proxy Publications Reporting Research Personnel Sampling Secondary Immunization Specificity Stains Structure of germinal center of lymph node T-Lymphocyte Teaching Materials Teenagers Testing Time United States National Institutes of Health Vaccination Vaccine Research Vaccines age group antigen-specific T cells booster vaccine cell type cohort improved individual response infancy lymph nodes model building novel vaccines outreach peripheral blood predictive modeling recruit response sex side effect single-cell RNA sequencing success transcriptome sequencing vaccination outcome vaccine response vaccine-induced immunity web platform web site

项目摘要

Project Summary/Abstract: Bordetella pertussis (PT) is the causative agent of whooping cough. Highly effective vaccines to protect from PT infection have been in use since the early 1940s. However, the last fifteen years have witnessed a consistent increase in the number of whooping cough cases, and the reasons for this are not completely understood. This highlights the need to better understand how immune responses against PT vary between individuals, which we can determine by measuring immune responses to PT booster vaccination as a proxy for immune responses to infectious challenge. We will use these data to develop computational models that will help establish a quantitative and predictive understanding of the factors that impact immune responses resulting from PT booster vaccination. Specifically, we will examine the impact of demographic variables such as age and sex, the type of vaccine received in infancy, and the immune state prior to vaccination. Understanding how these variables can impact vaccine responses is of importance not only for PT, but for vaccine research in general. To achieve this, we are proposing an iterative process of model building, model evaluation, experimental data generation, and model refinement. We will engage the wider scientific community in this process by hosting an annual prediction contest. We have placed particular emphasis on making this process transparent and open, to ensure that the value of the models and the results from the evaluation are accepted by the community at large. Specifically, we will: 1) Establish and seed an open platform to build and evaluate computational models of PT booster vaccination. 2) Generate new experimental data with staggered release dates to test and iteratively improve computational models. 3) Engage the broader scientific community in this modeling effort.

项目概要/摘要：百日咳杆菌（PT）是百日咳的病原体。高效的疫苗来保护 PT感染自20世纪40年代初以来一直在使用。然而，在过去的15年里，百日咳病例增加，其原因尚不完全清楚。这强调需要更好地了解个体之间对PT的免疫反应如何变化，我们可以通过测量对PT加强疫苗接种的免疫应答来确定，传染性挑战我们将使用这些数据来开发计算模型，这将有助于建立一个定量和预测的了解影响PT加强疫苗接种产生的免疫应答的因素。具体地说，我们将研究人口统计变量的影响，如年龄和性别，接种疫苗的类型，婴儿期和接种疫苗前的免疫状态。了解这些变量如何影响疫苗反应不仅对PT，而且对疫苗研究都很重要。为了实现这一点，我们提出了一个迭代的过程，模型建立，模型评估，实验数据生成和模型细化。我们将通过举办一个年度预测大赛我们特别强调使这一进程透明和公开，确保模型的价值和评估结果为社会大众所接受。具体而言，我们将： 1)建立并播种一个开放平台，用于构建和评估PT加强疫苗接种的计算模型。 2)生成具有交错发布日期的新实验数据以进行测试，并迭代地改进计算模型 3)让更广泛的科学界参与这项建模工作。