Function of asthma- and allergic disease-associated risk variants and genes in lung immune cells

肺免疫细胞中哮喘和过敏性疾病相关风险变异和基因的功能

• 批准号: 10453777
• 负责人: Anne I. Sperling
• 金额: $ 38.86万
• 依托单位: UNIVERSITY OF CHICAGO
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-07-19 至 2026-04-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10453777
• 关键词: Address; Adult; Affect; Allergic; Allergic Disease; Antigens; Asthma; B-Lymphocytes; Bacterial Artificial Chromosomes; Blood; Blood Cells; Bronchus-Associated Lymphoid Tissue; Candidate Disease Gene; Cell Line; Cells; Child; Chromatin; Clustered Regularly Interspaced Short Palindromic Repeats; Collaborations; Data; Databases; Dendritic Cells; Disease; Enhancers; Environment; Epithelial Cells; Gene Expression; Genes; Genetic; Genetic Risk; Genetic Variation; Genomics; Genotype-Tissue Expression Project; Goals; Human; Immune; Immune response; Immune system; Immunization; Immunologics; Incidence; Inflammatory; Knowledge; Ligands; Link; Lung; Lymphocyte; Lymphoid; Modeling; Myelogenous; Pathogenesis; Pathway interactions; Phenotype; Play; Population; Property; Publishing; Quantitative Trait Loci; Regulation; Regulatory Element; Resources; Role; Sampling; Smooth Muscle Myocytes; Spleen; T-Lymphocyte; Technology; Therapeutic; Tissue Model; Tissues; Transgenic Mice; Transgenic Organisms; United States; Variant; Virus; Whole Blood; Work; asthma exacerbation; base; causal variant; cell type; clinical heterogeneity; cytokine; disease heterogeneity; genetic variant; immune function; immunoregulation; in vivo; macrophage; new therapeutic target; novel; peripheral blood; programs; receptor function; response; risk variant

Asthma and allergic diseases (AADs) affect over 25 million children and adults in the United States, and AAD incidence has been increasing over the last 4 decades. There is significant clinical heterogeneity in AAD due to multiple overlapping but distinct underlying mechanisms of disease. Both innate and adaptive branches of the immune system play key roles in asthma pathogenesis and the heterogeneity of the disease. Yet, studies of immune cells in asthma have rely mostly on peripheral blood cells, which have different origins, composition, receptors and function than immune cells in the lung. Our work combined with those of others demonstrated that subsets of lung T cells, B cells, macrophages and dendritic cells have substantial differences from their counterparts in blood and other tissues. Thus, circulating immune cells are a poor model for tissue-based immune cells, and focus should shift toward lung-resident immune cells in studies of AADs. In Project 2, we focus on discovering mechanisms that guide the function of specific lung-resident immune cells and how genetic variation perturbs these mechanisms. The premise that most AAD-associated genetic variants impart their effects by changing the properties of cell type-specific regulatory elements thereby altering expression of target genes, implies that the phenotypic effects of these variants should be studied in homogenous populations of specific lung cells. Nevertheless, the largest public expression quantitative trait loci (eQTL) databases, such as GTEx, sample whole lung, which represents a mix of many different cell types. Nearly all that is known about genetic effects in immune cells are from studies of peripheral blood immune cells. As such, extrapolation of the effects of AAD risk variants from these resources are not likely to reflect their effects in AAD-relevant lung immune cells. Thus, our overall goal is to address these significant gaps by leveraging this collaborative program's unique resources to determine i) how specific lung immune cell types relevant to AADs contribute to immune responses, ii) the effects of genetic variation on these responses, iii) how different lung immune cell types coordinate to generate immune responses and how this is skewed by AAD-relevant inflammatory states, and iv) the functional effects on AAD causal variants and their target genes. We will achieve our goals through 3 Aims. Aim 1 will use human lymphoid and myeloid lung-resident immune cells to determine the landscape of stimulation-responsive genes, enhancers and stimulation-responsive chromatin and the effects of genetic variation on these responses. Aim 2 will determine how putative causal variants affect gene expression and downstream function in lung immune cells under asthma relevant conditions. Aim 3 will investigate the role of genetic variation identified through our omics studies on the in vivo response to allergic stimulation using CRISPR and BAC transgenic technology. Achieving our goals will link cells-specific mechanisms of immune regulation, genetic risk in AAD and specific genes, ultimately leading to treatments for asthma and allergic diseases.

哮喘和过敏性疾病（AAD）影响美国超过2500万儿童和成人， 在过去的40年里，发病率一直在上升。由于以下原因，AAD存在显著的临床异质性 多种重叠但不同的潜在疾病机制。先天和适应性的分支， 免疫系统在哮喘的发病机制和疾病的异质性中起关键作用。然而，研究 哮喘中免疫细胞主要依赖于外周血细胞，外周血细胞具有不同的来源、组成 受体和功能比肺中的免疫细胞。我们的工作与其他人的工作相结合， 肺T细胞、B细胞、巨噬细胞和树突状细胞的亚群与它们的细胞亚群具有实质性差异。 血液和其他组织中的对应物。因此，循环免疫细胞对于基于组织的免疫调节是一个很差的模型。 免疫细胞，重点应该转向肺部驻留的免疫细胞在抗AD的研究。在项目2中，我们 专注于发现指导特定肺部驻留免疫细胞功能的机制，以及如何 遗传变异扰乱了这些机制。大多数AAD相关遗传变异的前提是 通过改变细胞类型特异性调节元件的性质，从而改变 靶基因，这意味着这些变体的表型效应应该在同源的 特定的肺细胞群。然而，最大的公共表达数量性状基因座（eQTL） 数据库，如GTEx，对整个肺进行采样，这代表了许多不同细胞类型的混合。几乎所有 我们对免疫细胞遗传效应的了解来自于对外周血免疫细胞的研究。因此，在本发明的一个方面， 从这些资源中推断AAD风险变量的影响不太可能反映其在以下方面的影响： AAD相关肺免疫细胞。因此，我们的总体目标是通过利用这一点来解决这些重大差距。 合作计划的独特资源，以确定i）特定的肺免疫细胞类型如何与AAD相关 有助于免疫反应，ii）遗传变异对这些反应的影响，iii）不同的肺 免疫细胞类型协调产生免疫反应，以及这是如何被AAD相关 炎症状态，和iv）对AAD致病变体及其靶基因的功能作用。我们将 通过三个目标实现我们的目标。Aim 1将使用人类淋巴和骨髓肺驻留免疫细胞， 确定刺激响应基因、增强子和刺激响应染色质的景观 以及遗传变异对这些反应的影响。目标2将确定假定的因果变异 影响哮喘相关条件下肺免疫细胞的基因表达和下游功能。目的 3将研究通过我们的组学研究确定的遗传变异对体内应答的作用， 使用CRISPR和BAC转基因技术的过敏刺激。实现我们的目标将连接细胞特异性 免疫调节机制，AAD的遗传风险和特定基因，最终导致治疗 哮喘和过敏性疾病。