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1
The Research Progress in Immunotherapy of Tuberculosis.结核病免疫治疗的研究进展。
Front Cell Infect Microbiol. 2021 Nov 15;11:763591. doi: 10.3389/fcimb.2021.763591. eCollection 2021.
2
[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.
3
Antibiotic Treatment Shapes the Antigenic Environment During Chronic TB Infection, Offering Novel Targets for Therapeutic Vaccination.抗生素治疗在慢性结核感染期间塑造抗原环境,为治疗性疫苗接种提供新的靶标。
Front Immunol. 2020 Apr 28;11:680. doi: 10.3389/fimmu.2020.00680. eCollection 2020.
4
Tuberculosis结核病
5
Tuberculosis: current treatment, diagnostics, and newer antitubercular agents in clinical trials.结核病:当前的治疗、诊断方法以及临床试验中的新型抗结核药物
Infect Disord Drug Targets. 2015;15(1):32-41. doi: 10.2174/1871526514666140923153329.
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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.
7
The role of epigenetics, bacterial and host factors in progression of Mycobacterium tuberculosis infection.表观遗传学、细菌和宿主因素在结核分枝杆菌感染进展中的作用。
Tuberculosis (Edinb). 2018 Dec;113:200-214. doi: 10.1016/j.tube.2018.10.009. Epub 2018 Oct 30.
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[Annual progress of immunotherapy for tuberculosis in 2023].[2023年结核病免疫治疗年度进展]
Zhonghua Jie He He Hu Xi Za Zhi. 2024 Apr 12;47(4):371-375. doi: 10.3760/cma.j.cn112147-20231031-00283.
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Targeting multidrug-resistant tuberculosis (MDR-TB) by therapeutic vaccines.针对耐多药结核病(MDR-TB)的治疗性疫苗。
Med Microbiol Immunol. 2013 Apr;202(2):95-104. doi: 10.1007/s00430-012-0278-6. Epub 2012 Nov 10.
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[Frontier of mycobacterium research--host vs. mycobacterium].[分枝杆菌研究前沿——宿主与分枝杆菌]
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引用本文的文献

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Treatment outcomes and associated influencing factors among elderly patients with rifampicin-resistant tuberculosis: a multicenter, retrospective, cohort study in China.老年耐利福平肺结核患者的治疗结局及相关影响因素:一项中国的多中心、回顾性队列研究
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Cell therapies for viral diseases: a new frontier.用于病毒性疾病的细胞疗法:一个新的前沿领域。
Semin Immunopathol. 2025 Jan 2;47(1):5. doi: 10.1007/s00281-024-01031-8.
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Enhanced Immune Responses Against Through Heat-Killed BCG with Squalene-in-water Emulsion Adjuvant.通过水包角鲨烯乳液佐剂的热灭活卡介苗增强针对……的免疫反应。 (原文中“Against”后面缺少具体内容)
Indian J Microbiol. 2024 Dec;64(4):1929-1937. doi: 10.1007/s12088-024-01278-7. Epub 2024 May 27.
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Distinguish active tuberculosis with an immune-related signature and molecule subtypes: a multi-cohort analysis.鉴别具有免疫相关特征和分子亚型的活动性结核病:一项多队列分析。
Sci Rep. 2024 Nov 28;14(1):29564. doi: 10.1038/s41598-024-80072-3.
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IFNγ-secreting T cells that highly express IL-2 potently inhibit the growth of intracellular in macrophages.高表达 IL-2 的 IFNγ 分泌 T 细胞能够强有力地抑制巨噬细胞内的 生长。
Front Immunol. 2024 Nov 7;15:1469118. doi: 10.3389/fimmu.2024.1469118. eCollection 2024.
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The progress of drug targets.药物靶点的进展
Front Med (Lausanne). 2024 Oct 21;11:1455715. doi: 10.3389/fmed.2024.1455715. eCollection 2024.
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The advances in adjuvant therapy for tuberculosis with immunoregulatory compounds.用于结核病辅助治疗的免疫调节化合物的进展。
Front Microbiol. 2024 Jun 20;15:1380848. doi: 10.3389/fmicb.2024.1380848. eCollection 2024.
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hijacks host macrophages-derived interleukin 16 to block phagolysosome maturation for enhancing intracellular growth.劫持宿主巨噬细胞衍生的白细胞介素16以阻止吞噬溶酶体成熟,从而增强细胞内生长。
Emerg Microbes Infect. 2024 Dec;13(1):2322663. doi: 10.1080/22221751.2024.2322663. Epub 2024 Mar 3.
9
: immune response, biomarkers, and therapeutic intervention.免疫反应、生物标志物与治疗干预。
MedComm (2020). 2024 Jan 6;5(1):e419. doi: 10.1002/mco2.419. eCollection 2024 Jan.
10
Advanced drug delivery and therapeutic strategies for tuberculosis treatment.用于结核病治疗的先进药物输送和治疗策略。
J Nanobiotechnology. 2023 Nov 9;21(1):414. doi: 10.1186/s12951-023-02156-y.

本文引用的文献

1
A peptide-based vaccine ACP derived from antigens of Mycobacterium tuberculosis induced Th1 response but failed to enhance the protective efficacy of BCG in mice.一种来源于结核分枝杆菌抗原的基于肽的疫苗 ACP 诱导了 Th1 反应,但未能增强卡介苗在小鼠中的保护效力。
Indian J Tuberc. 2022 Oct;69(4):482-495. doi: 10.1016/j.ijtb.2021.08.016. Epub 2021 Aug 18.
2
Differential Diagnosis of Latent Tuberculosis Infection and Active Tuberculosis: A Key to a Successful Tuberculosis Control Strategy.潜伏性结核感染与活动性结核的鉴别诊断:成功结核病控制策略的关键
Front Microbiol. 2021 Oct 22;12:745592. doi: 10.3389/fmicb.2021.745592. eCollection 2021.
3
Vitamin D receptor activated by vitamin D administration alleviates Mycobacterium tuberculosis-induced bone destruction by inhibiting NFκB-mediated aberrant osteoclastogenesis.维生素 D 给药激活维生素 D 受体通过抑制 NFκB 介导的异常破骨细胞生成来减轻结核分枝杆菌引起的骨破坏。
FASEB J. 2021 Jun;35(6):e21543. doi: 10.1096/fj.202100135R.
4
Peptides-Based Vaccine MP3RT Induced Protective Immunity Against Infection in a Humanized Mouse Model.基于肽的疫苗 MP3RT 诱导针对 感染的保护免疫反应在人源化小鼠模型中。
Front Immunol. 2021 Apr 26;12:666290. doi: 10.3389/fimmu.2021.666290. eCollection 2021.
5
Prophylactic efficacy against Mycobacterium tuberculosis using ID93 and lipid-based adjuvant formulations in the mouse model.使用 ID93 和基于脂质的佐剂制剂在小鼠模型中预防结核分枝杆菌的功效。
PLoS One. 2021 Mar 11;16(3):e0247990. doi: 10.1371/journal.pone.0247990. eCollection 2021.
6
Trained immunity, tolerance, priming and differentiation: distinct immunological processes.训练免疫、耐受、致敏和分化:不同的免疫过程。
Nat Immunol. 2021 Jan;22(1):2-6. doi: 10.1038/s41590-020-00845-6.
7
Development of a formulation platform for a spray-dried, inhalable tuberculosis vaccine candidate.喷雾干燥型可吸入肺结核候选疫苗制剂平台的开发。
Int J Pharm. 2021 Jan 25;593:120121. doi: 10.1016/j.ijpharm.2020.120121. Epub 2020 Dec 2.
8
Extruded filaments derived 3D printed medicated skin patch to mitigate destructive pulmonary tuberculosis: design to delivery.挤出长丝 3D 打印载药皮肤贴片以减轻破坏性肺结核:从设计到交付。
Expert Opin Drug Deliv. 2021 Feb;18(2):301-313. doi: 10.1080/17425247.2021.1845648. Epub 2020 Nov 15.
9
DAR-901 vaccine for the prevention of infection with Mycobacterium tuberculosis among BCG-immunized adolescents in Tanzania: A randomized controlled, double-blind phase 2b trial.用于预防坦桑尼亚卡介苗免疫青少年感染结核分枝杆菌的DAR-901疫苗:一项随机对照、双盲2b期试验。
Vaccine. 2020 Oct 27;38(46):7239-7245. doi: 10.1016/j.vaccine.2020.09.055. Epub 2020 Sep 29.
10
Effects of Mycobacterium vaccae vaccine in a mouse model of tuberculosis: protective action and differentially expressed genes.卡介苗疫苗在结核分枝杆菌感染小鼠模型中的作用:保护作用及差异表达基因。
Mil Med Res. 2020 Jun 3;7(1):25. doi: 10.1186/s40779-020-00258-4.

结核病免疫治疗的研究进展。

The Research Progress in Immunotherapy of Tuberculosis.

机构信息

Tuberculosis Prevention and Control Key Laboratory/Beijing Key Laboratory of New Techniques of Tuberculosis Diagnosis and Treatment, Senior Department of Tuberculosis, The 8th Medical Center of PLA General Hospital, Beijing, China.

出版信息

Front Cell Infect Microbiol. 2021 Nov 15;11:763591. doi: 10.3389/fcimb.2021.763591. eCollection 2021.

DOI:10.3389/fcimb.2021.763591
PMID:34869066
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8634162/
Abstract

Tuberculosis (TB) is a serious public health problem worldwide. The combination of various anti-TB drugs is mainly used to treat TB in clinical practice. Despite the availability of effective antibiotics, effective treatment regimens still require long-term use of multiple drugs, leading to toxicity, low patient compliance, and the development of drug resistance. It has been confirmed that immune recognition, immune response, and immune regulation of () determine the occurrence, development, and outcome of diseases after infection. The research and development of TB-specific immunotherapy agents can effectively regulate the anti-TB immune response and provide a new approach toward the combined treatment of TB, thereby preventing and intervening in populations at high risk of TB infection. These immunotherapy agents will promote satisfactory progress in anti-TB treatment, achieving the goal of "ultra-short course chemotherapy." This review highlights the research progress in immunotherapy of TB, including immunoreactive substances, tuberculosis therapeutic vaccines, chemical agents, and cellular therapy.

摘要

结核病(TB)是全球严重的公共卫生问题。在临床实践中,多种抗结核药物的联合使用主要用于治疗结核病。尽管有有效的抗生素,有效的治疗方案仍需要长期使用多种药物,导致毒性、患者依从性低和耐药性的发展。已经证实,()对感染后疾病的发生、发展和结局的免疫识别、免疫反应和免疫调节起着决定性作用。结核特异性免疫治疗药物的研发可以有效地调节抗结核免疫反应,为结核的联合治疗提供新的途径,从而预防和干预结核感染高危人群。这些免疫治疗药物将促进抗结核治疗取得满意的进展,实现“超短程化疗”的目标。本文重点介绍了结核病免疫治疗的研究进展,包括免疫反应物质、结核治疗性疫苗、化学制剂和细胞治疗。