• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于研究感染的模型系统:科学潜力与障碍概述

Model systems to study infections: an overview of scientific potential and impediments.

作者信息

Nangpal Prachi, Nagpal Neha Lalwani, Angrish Nupur, Khare Garima

机构信息

Department of Biochemistry, University of Delhi, New Delhi, India.

出版信息

Front Cell Infect Microbiol. 2025 May 8;15:1572547. doi: 10.3389/fcimb.2025.1572547. eCollection 2025.

DOI:10.3389/fcimb.2025.1572547
PMID:40406522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12095297/
Abstract

Despite years of global efforts to combat tuberculosis (TB), (), the causative agent of this disease, continues to haunt the humankind making TB elimination a distant task. To comprehend the pathogenic nuances of this organism, various and experimental models have been employed by researchers. This review focuses on the salient features as well as pros and cons of various model systems employed for TB research. and macrophage infection models have been extensively used for studying physiology. Animal models have provided us with great wealth of information and have immensely contributed to the understanding of TB pathogenesis and host responses during infection. Additionally, they have been used for evaluation of anti-mycobacterial drug therapy as well as for determining the efficacy of potential vaccine candidates. Advancements in various 'omics' based approaches have enhanced our understanding about the host-pathogen interface. Although animal models have been the cornerstone to TB research, none of them is ideal that gives us a complete picture of human infection, disease and progression. Further, the review also discusses about the newer systems including three dimensional (3D)-tissue models, lung-on-chip infection model, TB granuloma model and their limitations for studying TB. Thus, converging information gained from various and models in tandem with experiments will ultimately bridge the gap that exists in understanding human TB.

摘要

尽管全球多年来致力于抗击结核病(TB),但该疾病的病原体结核分枝杆菌仍在困扰着人类,使得消除结核病成为一项遥远的任务。为了理解这种生物体的致病细微差别,研究人员采用了各种体外和实验模型。本综述重点关注用于结核病研究的各种模型系统的显著特征以及优缺点。体外和巨噬细胞感染模型已被广泛用于研究结核分枝杆菌生理学。动物模型为我们提供了大量信息,并极大地有助于理解感染期间的结核病发病机制和宿主反应。此外,它们还被用于评估抗分枝杆菌药物治疗以及确定潜在疫苗候选物的功效。基于各种“组学”方法的进展增强了我们对宿主 - 病原体界面的理解。尽管动物模型一直是结核病研究的基石,但没有一个是理想的,能让我们全面了解人类感染、疾病和进展情况。此外,本综述还讨论了包括三维(3D)组织模型、芯片肺感染模型、结核肉芽肿模型等较新的系统及其在研究结核病方面的局限性。因此,将从各种体外和体内模型以及体外实验中获得的信息结合起来,最终将弥合在理解人类结核病方面存在的差距。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5c2/12095297/49bb143b6b5f/fcimb-15-1572547-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5c2/12095297/5ac5476b306b/fcimb-15-1572547-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5c2/12095297/49bb143b6b5f/fcimb-15-1572547-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5c2/12095297/5ac5476b306b/fcimb-15-1572547-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5c2/12095297/49bb143b6b5f/fcimb-15-1572547-g002.jpg

相似文献

1
Model systems to study infections: an overview of scientific potential and impediments.用于研究感染的模型系统:科学潜力与障碍概述
Front Cell Infect Microbiol. 2025 May 8;15:1572547. doi: 10.3389/fcimb.2025.1572547. eCollection 2025.
2
Mouse models of human TB pathology: roles in the analysis of necrosis and the development of host-directed therapies.人类结核病病理学的小鼠模型:在坏死分析和宿主导向疗法开发中的作用。
Semin Immunopathol. 2016 Mar;38(2):221-37. doi: 10.1007/s00281-015-0538-9. Epub 2015 Nov 5.
3
Host-directed therapy targeting the Mycobacterium tuberculosis granuloma: a review.针对结核分枝杆菌肉芽肿的宿主导向治疗:综述
Semin Immunopathol. 2016 Mar;38(2):167-83. doi: 10.1007/s00281-015-0537-x. Epub 2015 Oct 28.
4
Editorial: Current status and perspective on drug targets in tubercle bacilli and drug design of antituberculous agents based on structure-activity relationship.社论:结核杆菌药物靶点的现状与展望以及基于构效关系的抗结核药物设计
Curr Pharm Des. 2014;20(27):4305-6. doi: 10.2174/1381612819666131118203915.
5
[Development of antituberculous drugs: current status and future prospects].[抗结核药物的研发:现状与未来前景]
Kekkaku. 2006 Dec;81(12):753-74.
6
Timing matters in macrophage/CD4+ T cell interactions: an agent-based model comparing host-pathogen interactions between latently infected and naïve individuals.巨噬细胞/CD4 + T细胞相互作用中的时间因素:一种基于主体的模型,比较潜伏感染个体和未感染个体之间的宿主-病原体相互作用。
mSystems. 2025 Mar 18;10(3):e0129024. doi: 10.1128/msystems.01290-24. Epub 2025 Feb 7.
7
Non-Human Primate Models of Tuberculosis.结核病的非人类灵长类动物模型。
Microbiol Spectr. 2016 Aug;4(4). doi: 10.1128/microbiolspec.TBTB2-0007-2016.
8
Harnessing Biological Insight to Accelerate Tuberculosis Drug Discovery.利用生物学洞察力加速结核病药物发现。
Acc Chem Res. 2019 Aug 20;52(8):2340-2348. doi: 10.1021/acs.accounts.9b00275. Epub 2019 Jul 30.
9
Heterogeneity in tuberculosis.结核病的异质性。
Nat Rev Immunol. 2017 Nov;17(11):691-702. doi: 10.1038/nri.2017.69. Epub 2017 Jul 24.
10
Cell death at the cross roads of host-pathogen interaction in Mycobacterium tuberculosis infection.结核分枝杆菌感染中宿主-病原体相互作用交叉点上的细胞死亡
Tuberculosis (Edinb). 2018 Dec;113:99-121. doi: 10.1016/j.tube.2018.09.007. Epub 2018 Sep 29.

本文引用的文献

1
Methods and Models for Studying in Respiratory Infections.研究呼吸道感染的方法与模型
Int J Mol Sci. 2024 Dec 24;26(1):18. doi: 10.3390/ijms26010018.
2
Advances in an In Vitro Tuberculosis Infection Model Using Human Lung Organoids for Host-Directed Therapies.利用人类肺类器官的体外结核感染模型进展:用于宿主导向治疗。
PLoS Pathog. 2024 Jul 25;20(7):e1012295. doi: 10.1371/journal.ppat.1012295. eCollection 2024 Jul.
3
The rabbit model for spinal tuberculosis: An overview.脊柱结核的兔模型:概述。
J Orthop Surg (Hong Kong). 2024 May-Aug;32(2):10225536241266703. doi: 10.1177/10225536241266703.
4
Mycobacterium tuberculosis strain with deletions in menT3 and menT4 is attenuated and confers protection in mice and guinea pigs.结核分枝杆菌 menT3 和 menT4 缺失株的减毒特性及其在小鼠和豚鼠中的保护作用。
Nat Commun. 2024 Jun 27;15(1):5467. doi: 10.1038/s41467-024-49246-5.
5
The breathtaking world of human respiratory in vitro models: Investigating lung diseases and infections in 3D models, organoids, and lung-on-chip.令人惊叹的人类呼吸体外模型世界:在 3D 模型、类器官和肺芯片中研究肺部疾病和感染。
Eur J Immunol. 2024 Mar;54(3):e2250356. doi: 10.1002/eji.202250356. Epub 2024 Feb 15.
6
Glutamine metabolism inhibition has dual immunomodulatory and antibacterial activities against Mycobacterium tuberculosis.谷氨酰胺代谢抑制对结核分枝杆菌具有双重免疫调节和抗菌活性。
Nat Commun. 2023 Nov 16;14(1):7427. doi: 10.1038/s41467-023-43304-0.
7
Early innate cell interactions with in protection and pathology of tuberculosis.早期固有细胞与分枝杆菌相互作用在结核病的保护和发病机制中的作用。
Front Immunol. 2023 Oct 27;14:1260859. doi: 10.3389/fimmu.2023.1260859. eCollection 2023.
8
Comparative pathology of experimental pulmonary tuberculosis in animal models.动物模型中实验性肺结核的比较病理学
Front Vet Sci. 2023 Oct 12;10:1264833. doi: 10.3389/fvets.2023.1264833. eCollection 2023.
9
Herp regulates intracellular survival of H37Ra in macrophages by regulating reactive oxygen species-mediated autophagy.Herp 通过调节活性氧介导的自噬来调节 H37Ra 在巨噬细胞中的细胞内存活。
mBio. 2023 Oct 31;14(5):e0153523. doi: 10.1128/mbio.01535-23. Epub 2023 Oct 6.
10
Initial immune response after exposure to or to SARS-COV-2: similarities and differences.初次免疫应答:接触 或 SARS-COV-2 后的异同。
Front Immunol. 2023 Aug 17;14:1244556. doi: 10.3389/fimmu.2023.1244556. eCollection 2023.