Plasma Cells in Health and Disease

健康和疾病中的浆细胞

• 批准号: 10621320
• 负责人: Ignacio E. Sanz
• 金额: $ 269.13万
• 依托单位: EMORY UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-06-25 至 2027-04-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10621320
• 关键词: Acute; Allergic Reaction; Animals; Antibodies; Antigens; Area; Autoimmune Diseases; Autoimmune Responses; B-Lymphocytes; Bioinformatics; Biological Response Modifier Therapy; Bone Marrow; COVID-19 pandemic; CRISPR/Cas technology; Cell Aging; Cell Compartmentation; Cell Differentiation process; Cell Maturation; Cell Survival; Cell physiology; Cells; Chromatin; Complementary DNA; Computer Analysis; DNA Methylation; Data Set; Development; Disease; EZH2 gene; Endowment; Ensure; Epigenetic Process; Foundations; Generations; Genetic Transcription; Genome engineering; Goals; Graft Rejection; Health; Heme; Heterogeneity; Human; Hypersensitivity; Immune system; Immunoglobulin A; Immunoglobulin G; Immunoglobulin M; Immunoglobulin-Secreting Cells; Infection; Information Dissemination; Institution; Investigation; Iron; Laboratory Personnel; Libraries; Longevity; Mediating; Memory; Memory B-Lymphocyte; Metabolic; Metabolism; Molecular; Nature; Pathogenicity; Pathway interactions; Plasma Cells; Plasmablast; Population; Preparation; Process; Production; Regulation; Research Personnel; Role; SIRT1 gene; Safety; Serology; Systemic Lupus Erythematosus; Transcriptional Regulation; Vaccination; Work; arm; autoreactivity; base; data sharing; design; effective therapy; epigenetic regulation; epigenomics; histone modification; human tissue; immune function; immunogenic; improved; methylation pattern; overexpression; programs; response; transcriptome; vaccine response

Antibody secreting cells (ASC) are responsible for both protective and pathogenic responses through the function of populations endowed with different function and longevity. Hence, major unmet need in human health and disease is a deep understanding of the processes that underlie ASC generation from different B cell precursors through separate differentiation pathways; the metabolic, transcriptional and epigenetic programs that underpin these processes, thereby promoting the generation of diverse ASC populations of different longevity and function; and how these processes may be subverted in SLE leading to expansion of pathogenic autoreactive plasma cells. Proper ASC function and dysregulation respectively provide protection in vaccination and infection and mediate multiple diseases including SLE and other autoimmune conditions, allergic reactions and transplant rejection. Thus, understanding the processes that regulate differentiation and survival of protective ASC while avoiding the accumulation of pathogenic ones is essential for our ability to improve vaccination and treat multiple antibody- mediated diseases. Over the previous cycle, despite the severe disruption caused by the COVID-19 pandemic for over a year, our work has contributed major progress in these areas that provides the foundation for this renewal application. Combined, our work will address the following concepts: Theme 1 - ASC heterogeneity in human healthy and autoimmune responses; Theme 2 - Molecular and epigenetic regulation of PC development and survival; Theme 3 - Metabolic regulation of ASC differentiation, function and survival; Theme 4: Microenvironment regulation of ASC formation, survival and function. These goals will be accomplished by highly interactive investigators through the following Projects and cores: Project 1. Epigenetic and metabolic mechanisms governing commitment to the long-lived plasma cell pool (Lund, PI). Project 2. Epigenetic programming of plasma cell heterogeneity and metabolism. (Boss, PI) Project 3. Role of Cellular Senescence in long-lived plasma cell generation. (Lee, PI) Project 4. Heterogeneity. Regulation and Function of Antibody-Secreting Cells in SLE (Sanz, PI) Core A. Administrative Core (Sanz, PI) Core B. Epigenomics, Bioinformatics, and Genome Engineering (Scharer, PI)

抗体分泌细胞(Asc)负责保护性和致病性反应。 通过赋予不同功能和长寿的人群的功能。因此，少校 在人类健康和疾病方面未得到满足的需要是对基础过程的深刻理解 不同B细胞前体通过不同的分化途径产生ASC； 支持这些过程的代谢、转录和表观遗传程序，从而 促进不同寿命和功能的不同ASC种群的产生；以及如何 这些过程在系统性红斑狼疮中可能被颠覆，导致病理性自身反应的扩大。 浆细胞。ASC功能正常和调节失调分别为 接种疫苗和感染并调节多种疾病，包括系统性红斑狼疮和其他自身免疫 条件、过敏反应和移植排斥反应。因此，了解 调节保护性ASC的分化和存活，避免积聚 致病抗体对我们提高疫苗接种和治疗多种抗体的能力至关重要- 媒介疾病。 在上一个周期，尽管新冠肺炎大流行对 一年多来，我们的工作在这些领域取得了重大进展，为 是次续期申请。结合起来，我们的工作将涉及以下概念：主题1- 人类健康和自身免疫反应中ASC的异质性；主题2-分子和 PC发育和存活的表观遗传调控；主题3-ASC的代谢调控 分化、功能与生存；主题4：ASC形成的微环境调节， 生存和功能。这些目标将由高度互动的调查人员通过 以下项目和核心： 项目1.管理对长寿老人承诺的表观遗传和代谢机制 浆细胞池(Lund，PI)。 项目2.浆细胞异质性和新陈代谢的表观遗传编程。(老板，PI) 项目3.细胞衰老在长寿命浆细胞生成中的作用。(李，派) 项目4.异质性。SLE(Sanz，Pi)中抗体分泌细胞的调节和功能 核心A.行政核心(SANZ，PI) 表观基因组学、生物信息学和基因组工程(Scharer，PI)

项目成果

Autoreactive monoclonal antibodies from patients with primary biliary cholangitis recognize environmental xenobiotics.

来自原发性胆管炎患者的自身反应性单克隆抗体识别环境异种生物。

• DOI: 10.1002/hep.29245
• 发表时间: 2017-09
• 期刊: Hepatology (Baltimore, Md.)
• 作者: Tanaka T;Zhang W;Sun Y;Shuai Z;Chida AS;Kenny TP;Yang GX;Sanz I;Ansari A;Bowlus CL;Ippolito GC;Coppel RL;Okazaki K;He XS;Leung PSC;Gershwin ME
• 通讯作者: Gershwin ME

Understanding B-cell activation and autoantibody repertoire selection in systemic lupus erythematosus: A B-cell immunomics approach.

• DOI: 10.1111/imr.12660
• 发表时间: 2018-07
• 期刊: Immunological reviews
• 影响因子: 8.7
• 作者: Tipton CM;Hom JR;Fucile CF;Rosenberg AF;Sanz I
• 通讯作者: Sanz I

Systemic lupus erythematosus: Extent and patterns of off-label use of rituximab for SLE.

• DOI: 10.1038/nrrheum.2016.191
• 发表时间: 2016-11-22
• 期刊: Nature reviews. Rheumatology
• 作者: Sanz I

New Perspectives in Rheumatology: May You Live in Interesting Times: Challenges and Opportunities in Lupus Research.

• DOI: 10.1002/art.40109
• 发表时间: 2017-08
• 期刊: Arthritis & rheumatology (Hoboken, N.J.)
• 作者: Sanz I

Immediate Reactions After the First Dose of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Messenger RNA Vaccines Do Not Preclude Second-Dose Administration.

• DOI: 10.1093/cid/ciab448
• 发表时间: 2021-12-06
• 期刊: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
• 作者: Vanijcharoenkarn K;Lee FE;Martin L;Shih J;Sexton ME;Kuruvilla ME
• 通讯作者: Kuruvilla ME