检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:钟如杰 杜建[1] ONG Rujie;DU Jian(Department of bacteriology&immunology,Beijing Tuberculosis and Thoracic Tumor earch Institute/Beijing Chest Hospital,Capital Medical University,Beijing 101149,China)
机构地区:[1]北京市结核病胸部肿瘤研究所/首都医科大学附属北京胸科医院细菌免疫室,北京101149
出 处:《中国病原生物学杂志》2024年第10期1248-1250,F0003,共4页Journal of Pathogen Biology
摘 要:结核病是一种慢性传染病,其治疗周期较长,且容易产生耐药性。这与结核杆菌诱导机体生成结核肉芽肿之间存在密切关系。为了系统地研究结核肉芽肿,出现了许多构建生物模型的方法。在本文献综述中分析了结核肉芽肿的形成机制,比较了现有的生物模型构建方法,并探讨了类器官技术在构建新型结核肉芽肿体外模型的潜力与挑战,旨在为研发新型抗结核药物及优化治疗方案提供一个全新切入点。Tuberculosis is a chronic infectious disease,which has a lengthy treatment cycle and a tendency to develop drug resistance.Thisissue is closely related to the formation of tuberculous granuloma induced by Mycobacterium tuberculosis.To systematically study tuberculous granulomas,various methods for constructing biological models have been developed.In this review,we analyzed the mechanism of tuberculousgranuloma formation,compared and contrasted existing methods for constructing biological models,and assessed the potential and challenges of using organoid technology to create innovative in vitro models of tuberculous granulomas.The goal is to provide a fresh perspective for the development of innovative anti-tuberculosis drugsand the optimization of treatment strategies.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.49