Role of Macrophage Migration Inhibitory Factor (MIF) in Pneumococcal Pathogenesis

巨噬细胞迁移抑制因子 (MIF) 在肺炎球菌发病机制中的作用

• 批准号: 8528463
• 负责人: Rituparna Das
• 金额: $ 13.38万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-30 至 2015-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8528463
• 关键词: Age; Antibiotics; Bacteria; Cessation of life; Child; Childhood; Communicable Diseases; Communities; Data; Defect; Disease; Doctor of Philosophy; Epithelium; Generations; Immune; Immune response; Immune system; Infection; Inflammation; Inflammatory; Inflammatory Response; Integration Host Factors; Laboratories; Lead; Location; Lower Respiratory Tract Infection; Lower respiratory tract structure; Lung; Mediating; Mediator of activation protein; Mentors; Mentorship; Migration Inhibitory Factor; Modeling; Morbidity - disease rate; Mucosal Immune Responses; Mus; Natural Immunity; Neutrophil Activation; Neutrophil Infiltration; Nose; Organism; Organism Strains; Pathogenesis; Patients; Pattern recognition receptor; Pennsylvania; Persons; Play; Pneumococcal Colonization; Pneumococcal Infections; Pneumococcal vaccine; Pneumonia; Population; Postdoctoral Fellow; Production; Research; Research Methodology; Research Personnel; Risk; Role; Site; Sterility; Streptococcus pneumoniae; Structure of mucous membrane of nose; Structure of parenchyma of lung; Surface; Tissues; Training; Training Programs; Universities; Upper respiratory tract; Work; base; career; chemokine; cytokine; macrophage; mortality; neutrophil; novel; pathogen; phenylpyruvate tautomerase; response; vaccination strategy

DESCRIPTION (provided by applicant): Despite the use of antibiotics and vaccines, Streptococcus pneumoniae (pneumococcus) remains a leading cause of community acquired pneumonia and mortality. Pneumococcal strains are maintained in the population as commensal colonizers of the mucosal surfaces of the upper respiratory tract (URT), which is a precursor to infection of the lower respiratory tract (LRT). Research to date indicates that the pneumococcus has a variety of interactions with the host immune system that are dictated by bacterial as well as host factors, and the anatomical location of the interface. Host factors that lead to the clearance of the bacterium from its commensal niche on the mucosal surface of URT are not well defined. Moreover, it is often the exuberance of the host inflammatory response that leads to morbidity and mortality in the case of invasive pneumococcal infection in the LRT. My preliminary data demonstrate an important role for macrophage migration inhibitory factor (MIF), a cytokine and upstream mediator of the innate immune response, in pneumococcal infection. In a model of nasal colonization with the organism, I have shown that MIF-deficient mice have a prominent defect in the ability to clear URT pneumococcal colonization. In contrast, MIF seems to play a detrimental role in murine LRT infection with pneumococcus. I have demonstrated that presence of MIF in this model is associated with increased local cytokine production and neutrophil influx, resulting in lung tissue destruction, bacterial dissemination, and greater mortality. My hypothesis for this K08 proposal is that MIF has a dual role in pneumococcal pathogenesis - it is necessary for macrophage mediated clearance of URT colonization, but also promotes inflammatory tissue damage in response to invasive infection in the LRT. In Aim#1, I will investigate the mechanism by which MIF promotes clearance of pneumococcal colonization in the URT by examining the role of MIF in macrophage recruitment, activation, and function. In Aim#2, I will explore the contribution of MIF to pathogenic neutrophil recruitment and activation in the LRT. At Yale, I began my training in research methodology and innate immunity to infectious pathogens as a PhD candidate as well as an infectious disease fellow in the laboratory of Dr. Richard Bucala, who serves as my co-mentor for this proposal. Now as a post-doctoral researcher at the University of Pennsylvania, with Dr. Jeffrey Weiser as my primary mentor, I plan to examine the mechanisms by which the immune system interacts with pneumococcus from colonization to disease. I have assembled a mentorship committee as well as a program of training throughout the course of this proposal that will serve as the basis for my career as an independent investigator examining the role of innate immunity in host-pathogen interactions. Pneumococcal disease remains a major cause of morbidity and mortality across the spectrum of age. Understanding the interaction between the immune system with the bacterium will allow us to appreciate how pneumococcus exists as a colonizer in the nasal mucosa but causes destructive invasive disease in the lungs. My work on the role of the host cytokine, macrophage migration inhibitory factor in both colonization and disease with the pathogen may lead to novel vaccination strategies, immune modulating therapies, or identification of patients at greatest risk for severe pneumococcal disease.

描述（由申请方提供）：尽管使用了抗生素和疫苗，但肺炎链球菌（肺炎球菌）仍然是社区获得性肺炎和死亡的主要原因。肺炎球菌菌株作为上呼吸道（URT）粘膜表面的肠道定殖者维持在人群中，这是下呼吸道（LRT）感染的前兆。迄今为止的研究表明，肺炎球菌与宿主免疫系统有多种相互作用，这些相互作用由细菌和宿主因素以及界面的解剖位置决定。导致细菌从URT粘膜表面上的细菌微生态位清除的宿主因素尚未明确。此外，在LRT中侵袭性肺炎球菌感染的情况下，通常是宿主炎症反应的旺盛导致发病和死亡。我的初步数据表明，在肺炎球菌感染的巨噬细胞移动抑制因子（MIF），细胞因子和先天免疫反应的上游介质的重要作用。在一个鼻腔定植模型中，我发现MIF缺陷小鼠在清除URT肺炎球菌定植的能力上存在明显缺陷。相反，MIF似乎在小鼠肺炎球菌LRT感染中起有害作用。我已经证明，在这个模型中，MIF的存在与局部细胞因子产生和中性粒细胞流入增加有关，导致肺组织破坏，细菌传播和更高的死亡率。我对K 08提案的假设是，MIF在肺炎球菌发病机制中具有双重作用-它是巨噬细胞介导的URT定植清除所必需的，但也促进了炎症组织损伤，以响应LRT中的侵入性感染。在目标#1中，我将通过研究MIF在巨噬细胞募集、激活和功能中的作用，研究MIF促进URT中肺炎球菌定植清除的机制。在目标2中，我将探讨MIF对LRT中致病性中性粒细胞募集和激活的贡献。在耶鲁大学，我作为博士生和理查德·布卡拉博士实验室的传染病研究员开始了对研究方法和传染性病原体先天免疫的培训，他是我这项提议的共同导师。现在，作为宾夕法尼亚大学的博士后研究员，Jeffrey Weiser博士是我的主要导师，我计划研究免疫系统与肺炎球菌从定植到疾病相互作用的机制。我已经组建了一个指导委员会，并在整个过程中进行了培训计划，这将成为我作为独立研究者的职业生涯的基础，研究先天免疫在宿主-病原体相互作用中的作用。肺炎球菌疾病仍然是各年龄段发病率和死亡率的主要原因。了解免疫系统与细菌之间的相互作用将使我们能够理解肺炎球菌如何在鼻粘膜中作为定植者存在，但在肺部引起破坏性侵入性疾病。我对宿主细胞因子，巨噬细胞迁移抑制因子在病原体定植和疾病中的作用的研究可能会导致新的疫苗接种策略，免疫调节疗法，或识别严重肺炎球菌疾病风险最大的患者。