FAIM in Immunity and Autoimmunity

免疫和自身免疫中的 FAIM

• 批准号: 8489252
• 负责人: THOMAS L ROTHSTEIN
• 金额: $ 38.62万
• 依托单位: FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-01 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8489252
• 关键词: Affect; Affinity; Antibodies; Antibody Formation; Antibody-Producing Cells; Antigens; Apoptosis; Attention; Autoantibodies; Autoimmune Diseases; Autoimmune Process; Autoimmunity; Autologous; B cell differentiation; B-Cell Activation; B-Lymphocytes; BCL1 Oncogene; Bacterial Infections; Binding; Biological Models; Biology; Blood; Cell physiology; Cellular biology; Clinical; Complex; DNA; Development; Disease; Down-Regulation; Dysplasia; Evolution; Face; Genes; Goals; Grant; Human; IRF4 gene; Immune; Immune response; Immunity; Immunoglobulins; In Vitro; Laboratories; Letters; Leukocytes; Location; Lower Organism; Lupus; Lupus Erythematosus; MS4A1 gene; Mature B-Lymphocyte; Modeling; Molecular Structure; Molecular Target; Mus; Participant; Patients; Personal Communication; Physiology; Plasma Cells; Play; Porifera; Process; Production; Protein Region; Proteins; Publishing; Research Personnel; Rest; Role; Sequence Homology; Signal Transduction; Specificity; Structure; Structure of germinal center of lymph node; System; TNFRSF5 gene; TNFSF5 gene; Time; Virus Diseases; Work; antimicrobial; fascinate; feeding; gene cloning; gene discovery; in vivo; lupus prone mice; new therapeutic target; novel; overexpression; plasma cell differentiation; public health relevance; therapeutic target; transcription factor

DESCRIPTION (provided by applicant): Like the two faces of Janus, antibodies can be a gateway to anti-microbial immunity or to autoantibody- associated disease. The recent successful use of anti-CD20 to treat patients with autoimmune dyscrasias has re-focused attention on the role of B cells as therapeutic targets. Mature B cells become antibody secreting plasma cells through a complex process that begins in the germinal center and involves alterations in multiple transcription factors. Work from this laboratory has identified a new player in B cell activation and differentiation, namely the novel gene, Faim. FAIM is unique; it is highly evolutionarily conserved, yet does not contain sequence homology, or structural homology, with any other protein. In B cells FAIM acts as a force multiplier. It boosts CD40 signaling by enhancing CD40L-stimulated increases in NF-:B and IRF4, and, it enhances the CD40L-stimulated decline in BCL-6. As expected from the extra increase in IRF4 and decline in BCL-6 (as well as its location in the germinal center) FAIM overexpression augments the plasma cell compartment in chimeric mice. FAIM expression is stimulated by IRF4 and so once triggered FAIM is involved in a "feed-forward" positive re-inforcing mechanism. The long term objective of this proposal is two-fold: to understand normal B cell biology focusing on how "resting" B cells become effectors, and to determine the points at which these processes go awry resulting in autoantibody production and autoimmunity. The near term objective of this work is to define the role of FAIM in facilitating immunity and regulating autoimmunity, with the goal of identifying a new therapeutic target. The specific aims of this proposal are to: 1) conduct a careful molecular structure/function analysis to identify and characterize the unique FAIM effector motif; and, 2) evaluate the influence of FAIM on the quality and selection of antibody produced in a model normal immune response, and on checkpoint integrity in a model system of spontaneous autoantibody production, and elucidate the physiology of FAIM expression in the germinal center. The results of this work are highly likely to provide completely new and fundamental information about how signaling in B cells is promoted, and about how plasma cell differentiation is regulated. Moreover, the recent finding by other investigators (unpublished) that SNPs proximal to, and within, the FAIM sequence are strongly associated with human lupus disease indicates that the mechanisms revealed by this study are highly likely to be relevant to understanding clinical autoimmunity and may provide a new target for therapeutic manipulation.

描述（由申请人提供）：就像Janus的两面一样，抗体可以成为抗微生物免疫或自身抗体相关疾病的门户。最近成功使用抗cd20治疗自身免疫性疾病患者重新关注了B细胞作为治疗靶点的作用。成熟的B细胞通过一个复杂的过程成为分泌抗体的浆细胞，该过程始于生发中心，涉及多种转录因子的改变。该实验室的工作已经确定了B细胞激活和分化的新参与者，即新基因Faim。饥荒是独一无二的；它是高度进化保守的，但不包含序列同源性，或结构同源性，与任何其他蛋白质。在B细胞中，饥饿是一种力量倍增器。它通过增强cd40l刺激的NF-:B和IRF4的增加来促进CD40信号传导，并增强cd40l刺激的BCL-6的下降。正如预期的那样，IRF4的额外增加和BCL-6的下降（以及它在生发中心的位置），FAIM过表达增加了嵌合小鼠的浆细胞区室。FAIM的表达是由IRF4刺激的，因此一旦触发FAIM就参与了一个“前馈”正向强化机制。这项建议的长期目标有两个方面：了解正常的B细胞生物学，重点关注“静止”B细胞如何成为效应细胞，并确定这些过程出错导致自身抗体产生和自身免疫的点。这项工作的近期目标是确定fam在促进免疫和调节自身免疫中的作用，目的是确定一个新的治疗靶点。本提案的具体目的是：1)进行仔细的分子结构/功能分析，以识别和表征独特的fam效应基序；2)评估FAIM对模型正常免疫反应中产生的抗体质量和选择的影响，以及对自发自身抗体产生模型系统中检查点完整性的影响，并阐明FAIM在生发中心表达的生理学。这项工作的结果极有可能为B细胞信号传导如何促进以及浆细胞分化如何调节提供全新的基础信息。此外，最近其他研究人员（未发表）发现，fam序列附近和内部的snp与人类狼疮疾病密切相关，这表明本研究揭示的机制极有可能与理解临床自身免疫相关，并可能为治疗操作提供新的靶点。