An Integrated Multilevel Modeling Framework for Repertoire-Based Diagnostics

用于基于指令的诊断的集成多级建模框架

• 批准号: 10910349
• 负责人: Ramy Arnaout
• 金额: $ 18.23万
• 依托单位: BETH ISRAEL DEACONESS MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-05-15 至 2025-04-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10910349
• 关键词: Address; Affect; Aging; Agreement; Amino Acid Motifs; Amino Acids; Antibodies; Autoimmune Diseases; Autoimmunity; B-Lymphocytes; Base Sequence; Big Data; Binding; Biophysics; Characteristics; Charge; Classification; Clinical; Collection; Complex; Computer Models; Creativeness; Data Set; Dependence; Diagnosis; Diagnostic; Diagnostic tests; Disease; Ensure; Entropy; Fostering; Gene Frequency; Genes; Goals; Health; Human; Immune; Immunology; Individual; Infection; Influenza vaccination; Intuition; Learning; Letters; Machine Learning; Malignant Neoplasms; Mathematics; Measurement; Measures; Medicine; Methods; Mission; Modeling; Outcome; Pattern; Performance; Persons; Physics; Play; Population Heterogeneity; Privatization; Property; Public Health; Reading; Reporting; Research; Role; Sample Size; Sampling; Sampling Errors; Signs and Symptoms; Speed; System; T-Cell Receptor; T-Cell Receptor Genes; T-Lymphocyte; Testing; United States National Institutes of Health; Vaccination; Virus Diseases; Work; biophysical properties; clinical diagnostics; computerized tools; diagnostic accuracy; human disease; immunological diversity; improved; innovation; machine learning method; multidisciplinary; multilevel analysis; novel; novel strategies; tool

Immune-repertoire sequence, which consists of an individual's millions of unique antibody and T-cell receptor (TCR) genes, encodes a dynamic and highly personalized record of an individual's state of health. Our long- term goal is to develop the computational models and tools necessary to read this record, to one day be able diagnose diverse infections, autoimmune diseases, cancers, and other conditions directly from repertoire se- quence. The key problem is how to find patterns of specific diseases in repertoire sequence, when repertoires are so complex. Our hypothesis is that a combination of bottom-up (sequence-level) and top-down (systems- level) modeling can reveal these patterns, by encoding repertoires as simple but highly informative models that can be used to build highly sensitive and specific disease classifiers. In preliminary studies, we introduced two new modeling approaches for this purpose: (i) statistical biophysics (bottom-up) and (ii) functional diversity (top-down), and showed their ability to elucidate patterns related to vaccination status (97% accuracy), viral infection, and aging. Building on these studies, we will test our hypothesis through two specific aims: (1) We will develop models and classifiers based on the bottom-up approach, statistical biophysics; and (2) we will de- velop the top-down approach, functional diversity, to improve these classifiers. To achieve these aims, we will use our extensive collection of public immune-repertoire datasets, beginning with 391 antibody and TCR da- tasets we have characterized previously. Our team has deep and complementary expertise in developing computational tools for finding patterns in immune repertoires (Dr. Arnaout) and in the mathematics that under- lie these tools (Dr. Altschul), with additional advice available as needed regarding machine learning (Dr. AlQuraishi). This proposal is highly innovative for how our two new approaches address previous issues in the field. (i) Statistical biophysics uses a powerful machine-learning method called maximum-entropy modeling (MaxEnt), improving on past work by tailoring MaxEnt to learn patterns encoded in the biophysical properties (e.g. size and charge) of the amino acids that make up antibodies/TCRs; these properties ultimately determine what targets antibodies/TCRs can bind, and therefore which sequences are present in different diseases. (ii) Functional diversity fills a key gap in how immunological diversity has been measured thus far, by factoring in whether different antibodies/TCRs are likely to bind the same target. This proposal is highly significant for (i) developing an efficient, accurate, generative, and interpretable machine-learning method for finding diagnostic patterns in repertoire sequence; (ii) applying a robust mathematical framework to the measurement of immuno- logical diversity; (iii) impacting clinical diagnostics; and (iv) adding a valuable new tool for integrative/big-data medicine. The expected outcome of this proposal is an integrated pair of robust and well validated new tools/models for classifying specific disease exposures directly from repertoire sequence. This proposal in- cludes plans to make these tools widely available, to maximize their positive impact across medicine.

免疫替代序列，由个人的数百万抗体和T细胞受体组成 （TCR）基因编码个人健康状况的动态和个性化的记录。我们的长期 术语目标是开发读取此记录所需的计算模型和工具，有一天能够 诊断出多种感染，自身免疫性疾病，癌症和其他疾病直接来自曲目 quence。关键问题是如何在曲目序列中找到特定疾病的模式 是如此复杂。我们的假设是自下而上（序列级）和自上而下的组合（系统 - 级别的建模可以通过将曲目编码为简单但信息丰富的模型来揭示这些模式 可用于构建高度敏感和特定的疾病分类器。在初步研究中，我们介绍了 为此目的的两种新建模方法：（i）统计生物物理学（自下而上）和（ii）功能多样性 （自上而下），并显示了他们阐明与疫苗接种状态相关的模式（精度为97％），病毒 感染和衰老。在这些研究的基础上，我们将通过两个具体目标检验我们的假设：（1）我们 将根据自下而上的方法，统计生物物理学开发模型和分类器； （2）我们将 从自上而下的方法，功能多样性，以改善这些分类器。为了实现这些目标，我们将 使用我们广泛的公共免疫替代数据集，从391抗体和TCR DA-开始 我们以前已经表征了Taset。我们的团队在发展方面具有深厚的互补专业知识 用于在免疫曲目中查找模式的计算工具（Arnaout博士）以及数学不足的数学 说出这些工具（Altschul博士），并根据需要提供有关机器学习的其他建议（博士 Alquraishi）。该提案对于我们的两种新方法如何解决以前的问题是高度创新的 场地。 （i）统计生物物理学使用一种强大的机器学习方法，称为最大入侵建模 （Maxent），通过调整Maxent学习生物物理特性中编码的模式来改善过去的工作 构成抗体/TCR的氨基酸的（例如大小和电荷）；这些属性最终确定 靶向抗体/TCR可以结合的是什么，因此在不同的疾病中存在哪些序列。 （ii） 功能多样性填补了迄今为止通过考虑到迄今为止免疫学多样性的关键差距 不同的抗体/TCR是否可能结合相同的靶标。该建议对于（i）非常重要 开发一种有效，准确，生成和可解释的机器学习方法，以查找诊断 曲目序列中的模式； （ii）将强大的数学框架应用于免疫的测量 逻辑多样性； （iii）影响临床诊断； （iv）为综合/大数据添加有价值的新工具 药品。该提案的预期结果是一对综合的稳健且经过良好验证的新的 直接从曲目序列中直接对特定疾病暴露进行分类的工具/模型。这项提议中 Cludes计划将这些工具广泛使用，以最大程度地发挥其在药物上的积极影响。