Genome-wide dissection of Mendelian susceptibility to mycobacterial disease

孟德尔对分枝杆菌疾病易感性的全基因组解析

• 批准号: 8460157
• 负责人: Jean-Laurent Casanova
• 金额: $ 39.72万
• 依托单位: ROCKEFELLER UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-05-01 至 2016-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8460157
• 关键词: Accounting; Affect; Antibiotics; BCG Vaccine; Biological; Candidate Disease Gene; Child; Childhood; Clinical; Communicable Diseases; Defect; Development; Disease; Dissection; Dominant Genetic Conditions; Employee Strikes; Family; Family member; Funding; Genes; Genetic; Genetic Counseling; Genetic Heterogeneity; Genetic Predisposition to Disease; Genus Mycobacterium; Grant; Hematopoietic Stem Cell Transplantation; Hereditary Disease; Herpes encephalitis; Heterogeneity; Host Defense; Human; IFNGR1 gene; IFNGR2 gene; IL12B gene; IL12RB1 gene; IL12RB2 gene; Immunity; Immunologic Deficiency Syndromes; Inborn Genetic Diseases; Individual; Infection; Interferon Receptor; Interferons; Interleukin-12; Investigation; JAK2 gene; Laboratories; Life; Light; Link; Maps; Mediating; Methods; Minority; Molecular Diagnosis; Molecular Genetics; Mutation; Pathogenesis; Pathway interactions; Patients; Physicians; Pneumococcal Infections; Predisposition; Recombinant Interferon; Recombinants; Recurrence; Research; Role; STAT1 gene; Salmonella infections; Syndrome; TYK2; Testing; Tuberculosis; Ubiquitin; United States National Institutes of Health; Ursidae Family; Variant; Viral; Virulent; Work; autosomal recessive trait; base; congenital immunodeficiency; cytokine; deep sequencing; disease-causing mutation; exome; exome sequencing; genome wide association study; genome-wide; genome-wide linkage; innovation; insight; microorganism; mycobacterial; novel; protein expression; public health relevance; recessive genetic trait; trait

DESCRIPTION (provided by applicant): Mendelian susceptibility to mycobacterial disease (MSMD) is a primary immunodeficiency syndrome characterized by severe disease caused by weakly virulent mycobacteria, such as BCG vaccines and environmental mycobacteria, in otherwise healthy patients. Patients with MSMD are also vulnerable to tuberculosis and salmonellosis, though other infections are rare. First described clinically in the 1950s, the pathogenesis of MSMD remained unclear until 1996, when its first genetic etiology was deciphered in children with interferon- receptor 1 (IFN-R1) deficiency. Genetic dissection of MSMD over the last fifteen years has identified six morbid genes, including five autosomal (IFNGR1, IFNGR2, STAT1, IL12B, IL12RB1) and one X- linked (NEMO) gene. The high level of allelic heterogeneity at these six loci has led to the definition of up to 13 distinct disorders. The pathogenesis of MSMD in patients with these disorders involves impaired interleukin-12 (IL-12)-dependent IFN- immunity. However, only about half of the 600 patients tested in our laboratory carried any of these genetic defects. We hypothesize that MSMD in other patients results from other monogenic inborn errors of immunity, possibly but not necessarily involving the IL-12-IFN- circuit. A hypothesis-based, candidate gene approach focused on genes involved in the IL-12-IFN- circuit and related to the known MSMD-causing genes is being funded by the NIH grant 1R01AI089970. Therefore, the principal objective of the work described in this application is to identify new MSMD-causing genes by following a complementary, hypothesis-generating, genome-wide (GW) screening approach. In the present, GW approach, we will search for and characterize MSMD-causing genes by GW linkage (for both X-linked and autosomal recessive traits) and GW deep sequencing (by whole-exome sequencing). A novel method of GW linkage has been developed in the lab and whole-exome deep sequencing has been pioneered by our lab for other infectious diseases. Following this approach, we have obtained strong preliminary evidence of five novel MSMD-causing genes, with recessive mutations in X-linked CYBB and autosomal TYK2, JAK2, ISG15, and AP4E1. These five discoveries are very surprising, each in a unique way, and together they neatly illustrate the power of GW approaches and whole-exome sequencing in particular. Our project is therefore highly innovative, feasible, and supported by strong preliminary evidence. From a basic biological standpoint, this research will provide considerable and novel insights into the mechanisms of immunity to mycobacteria. Elucidation of the molecular genetic basis of MSMD will also shed light on the pathogenesis of mycobacterial disease, making it possible to provide molecular diagnoses for patients and genetic counseling for families. This new information will pave the way for the use of IFN- or other cytokines for the treatment of mycobacterial diseases, in addition to antibiotics. Finally, the genetic dissection of MSMD will pave the way for the genetic dissection of severe tuberculosis in otherwise healthy children.

描述（由申请人提供）：分枝杆菌病孟德尔易感性（MSMD）是一种原发性免疫缺陷综合征，其特征是由弱毒分枝杆菌引起的严重疾病，如卡介苗和环境分枝杆菌，在其他健康患者中。MSMD患者也容易感染结核病和沙门氏菌病，尽管其他感染很少见。MSMD的发病机制在20世纪50年代首次被临床描述，直到1996年才在干扰素受体1 （IFN-R1）缺乏的儿童中发现其第一个遗传病因。在过去的15年里，MSMD的遗传解剖已经确定了6个病态基因，包括5个常染色体基因（IFNGR1、IFNGR2、STAT1、IL12B、IL12RB1）和1个X连锁（NEMO）基因。这6个基因座的高水平等位基因异质性导致了多达13种不同疾病的定义。这些疾病患者的MSMD发病机制涉及白细胞介素-12 （IL-12）依赖性IFN-免疫受损。然而，在我们实验室测试的600名患者中，只有大约一半的人携带这些遗传缺陷。我们假设其他患者的MSMD是由其他单基因先天性免疫错误引起的，可能但不一定涉及IL-12-IFN-回路。一种基于假设的候选基因方法专注于参与IL-12-IFN通路的基因，并与已知的msmd引起基因相关，该方法由NIH资助1R01AI089970。因此，本应用中描述的工作的主要目标是通过一种互补的、产生假设的、全基因组（GW）筛选方法来识别新的msmd引起基因。在目前的GW方法中，我们将通过GW连锁（x连锁和常染色体隐性性状）和GW深度测序（全外显子组测序）来寻找和表征msmd引起基因。我们的实验室已经开发了一种新的GW连锁方法，并在其他传染病的全外显子组深度测序方面开创了先河。根据这种方法，我们已经获得了5种新的msmd致病基因的强有力的初步证据，这些基因在x连锁CYBB和常染色体TYK2、JAK2、ISG15和AP4E1中具有隐性突变。这五个发现非常令人惊讶，每一个都以独特的方式出现，它们巧妙地说明了GW方法的力量，特别是全外显子组测序。因此，我们的项目具有高度的创新性和可行性，并得到了强有力的初步证据的支持。从基本生物学的角度来看，这项研究将为分枝杆菌的免疫机制提供可观的和新颖的见解。阐明MSMD的分子遗传学基础，也将有助于阐明分枝杆菌病的发病机制，为患者提供分子诊断，为家庭提供遗传咨询。这一新信息将为使用IFN-或其他细胞因子治疗分枝杆菌疾病铺平道路，除了抗生素。最后，MSMD的基因解剖将为其他健康儿童重症结核病的基因解剖铺平道路。