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Impact of Obesity and Weight-Loss Interventions on Immune-Surveillance Mechanisms

肥胖和减肥干预措施对免疫监视机制的影响

基本信息

批准号：
8322274
负责人：
VISHWA DEEP DIXIT
金额：
$ 5.12万
依托单位：
LSU PENNINGTON BIOMEDICAL RESEARCH CTR
依托单位国家：
美国
项目类别：
财政年份：
2011
资助国家：
美国
起止时间：
2011-04-01 至 2015-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8322274
关键词：
Adipocytes Antigens Biomedical Research Body Weight decreased Body mass index Bone Marrow Transplantation Caloric Restriction Cardiovascular Diseases Cell physiology Cells Cellular Immunity Chronic Clinical Research Data Deposition Detection Development Disease Endocrine Functional disorder Funding Gastrectomy Generations Goals Human Immune Immune System Diseases Immune system Immunity Immunologic Surveillance Incidence Infection Inflammation Institutional Review Boards Lead Lipids Liver Malignant Neoplasms Mediating Memory Metabolic Modeling Monkeys Mus Muscle Natural regeneration Nature Obesity Obesity associated disease Organ Outcome Participant Patients Phenotype Procedures Process Production Protocols documentation Research Research Personnel Risk Risk Assessment Schedule Severities Site T-Cell Receptor T-Lymphocyte Testing Thymus Gland adipocyte differentiation age related bariatric surgery base cell mediated immune response immune function immunosenescence lipid biosynthesis middle age mouse model novel pathogen post intervention prevent reconstitution vaccination strategy weight loss intervention

项目摘要

DESCRIPTION (provided by applicant): Robust T cell mediated immune responses are key components of protection from infection and certain cancers. Emerging evidence suggests that, apart from increased incidence of cardiovascular diseases and cancers, obesity also compromises T cell dependent immune-surveillance mechanisms in mice with increased risk and severity of infections. It is recognized that thymic export of T cells establishes the size and diversity of human naive T cell repertoire. Intriguingly, by middle age, thymus undergoes a process of involution characterized by reduced naive T cell production together with replacement of thymic space with adipocytes. Dietary-obesity is known to increase lipid deposition in several ectopic sites such as muscle, liver and compromise organ function. Similarly, we have shown that obesity in mice exacerbates the mechanisms that promote deposition of ectopic lipid-bearing adipocyte in thymus and reduces generation of naive T cells from thymus. Based on our data from mouse models that obesity restricts T cell receptor (TCR) repertoire diversity and preliminary findings in obese humans, we propose to test the hypothesis that, obesity accelerates immunosenescence and excess weight-loss can rescue loss of thymopoiesis and restriction of T cell repertoire diversity and function in humans. The overall goal of this project is to assess specific hypotheses and predictions about the relationship between obesity and immune system - in particular, thymopoiesis and T cell-mediated immunity - with implications for understanding the mechanisms whereby weight-loss might enhance immune- surveillance in humans. Therefore, we propose to study the impact of obesity and subsequent weight-loss through bariatric surgery and caloric restriction on functional thymic content, thymopoiesis, T cell function and TCR diversity in humans. We propose three specific aims, 1) To test the prediction that obesity increases ectopic adipocyte development in thymus. 2) To test the prediction that obesity lowers thymopoiesis and compromises T cell function. 3) To test the prediction that obesity-induced reduction in functional thymic space, thymopoiesis, and aberrant immune function can be rescued by weight-loss therapy.

描述（由申请人提供）：强大的T细胞介导的免疫应答是保护免受感染和某些癌症的关键组成部分。新出现的证据表明，除了心血管疾病和癌症的发病率增加外，肥胖还损害了小鼠的T细胞依赖性免疫监视机制，增加了感染的风险和严重程度。人们认识到，T细胞的胸腺输出建立了人幼稚T细胞库的大小和多样性。有趣的是，到了中年，胸腺经历了一个退化的过程，其特征是幼稚T细胞的产生减少，胸腺空间被脂肪细胞取代。已知饮食性肥胖会增加几个异位部位（如肌肉、肝脏）的脂质沉积，并损害器官功能。同样地，我们也发现小鼠肥胖加剧了促进胸腺异位脂质脂肪细胞沉积的机制，并减少了胸腺幼稚T细胞的产生。基于我们从肥胖限制T细胞受体（TCR）库多样性的小鼠模型中获得的数据和在肥胖人类中的初步发现，我们提出测试以下假设：肥胖加速免疫衰老和过度减肥可以挽救人类中胸腺生成的丧失和T细胞库多样性和功能的限制。该项目的总体目标是评估关于肥胖和免疫系统之间关系的具体假设和预测-特别是胸腺生成和T细胞介导的免疫-对理解减肥可能增强人类免疫监视的机制的影响。因此，我们建议研究肥胖和随后的减肥，通过减肥手术和热量限制功能性胸腺含量，胸腺生成，T细胞功能和TCR的多样性在人类的影响。我们提出了三个具体目标：1）检验肥胖增加胸腺异位脂肪细胞发育的预测。2)为了验证肥胖会降低胸腺细胞生成并损害T细胞功能的预测。3)验证肥胖引起的功能性胸腺空间减少、胸腺生成和异常免疫功能可以通过减肥治疗来挽救的预测。