• 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

针对不同分枝杆菌属结核杆菌谱系的再感染的保护作用广泛存在。

Protection against reinfection with extends across heterologous Mtb lineages.

作者信息

Simonson Andrew W, Chao Michael C, Hood Luke E, Donlan Rachel A, Hopkins Forrest, Chase Michael R, Vickers Andrew J, Callendrello Alanna, Klein Edwin, Borish H Jacob, Malin Marshall, Maiello Pauline, Scanga Charles A, Lin Philana Ling, Fortune Sarah M, Flynn JoAnne L

机构信息

Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

Center for Vaccine Research, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

出版信息

bioRxiv. 2025 Jul 31:2025.07.08.663727. doi: 10.1101/2025.07.08.663727.

DOI:10.1101/2025.07.08.663727
PMID:40672196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12265691/
Abstract

Immunological memory elicited either through previous or ongoing (Mtb) infection provides a critical mechanism by which hosts protect against re-infection and disease progression upon Mtb re-exposure. Conversely, the uneven competition between distinct Mtb strains suggest certain bacterial clades have enhanced ability to spread across communities and circulate globally, potentially by evading memory responses gained by prior infection with genomically different strains. To address whether memory responses induced by one strain can protect against a genetically distinct strain, we conducted a heterologous reinfection study in cynomolgus macaques involving primary infection by a Lineage 4 Erdman Mtb strain and subsequent re-challenge by a Lineage 2 strain, HT-L2. Recent epidemiologic studies have shown that the clade to which HT-L2 belongs has been spreading successfully over the last decade in Lima, Peru. Here, through microbiologic, PET-CT imaging and sequencing of Mtb genomic barcodes, we show that reinfected animals developed fewer lung lesions and controlled both pulmonary and disseminated forms of infection better than naïve animals without prior exposure to Mtb. Our data support that protection against reinfection is not limited by Mtb lineage, providing optimism that vaccines can be effective across populations and geographic locations.

摘要

通过既往或正在进行的(结核分枝杆菌)感染引发的免疫记忆提供了一种关键机制,宿主借此在再次接触结核分枝杆菌时预防再次感染和疾病进展。相反,不同结核分枝杆菌菌株之间的不均衡竞争表明,某些细菌进化枝具有更强的能力在社区中传播并在全球范围内循环,这可能是通过逃避先前感染基因组不同菌株所获得的记忆反应来实现的。为了探究由一种菌株诱导的记忆反应是否能抵御基因不同的菌株,我们在食蟹猴中进行了一项异源再感染研究,包括先用4型埃尔德曼结核分枝杆菌菌株进行初次感染,随后用2型菌株HT-L2进行再次攻击。最近的流行病学研究表明,HT-L2所属的进化枝在过去十年中在秘鲁利马成功传播。在此,通过微生物学、PET-CT成像以及结核分枝杆菌基因组条形码测序,我们发现再感染的动物肺部病变较少,并且比未接触过结核分枝杆菌的天真动物能更好地控制肺部和播散性感染形式。我们的数据支持对再感染的保护不受结核分枝杆菌谱系的限制,这为疫苗在不同人群和地理位置都能有效提供了乐观的依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/f768ea401849/nihpp-2025.07.08.663727v2-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/e8deff08fb83/nihpp-2025.07.08.663727v2-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/18f364663479/nihpp-2025.07.08.663727v2-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/55f7be953b94/nihpp-2025.07.08.663727v2-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/3b9b0dabf1a9/nihpp-2025.07.08.663727v2-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/cb736bb6367b/nihpp-2025.07.08.663727v2-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/f768ea401849/nihpp-2025.07.08.663727v2-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/e8deff08fb83/nihpp-2025.07.08.663727v2-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/18f364663479/nihpp-2025.07.08.663727v2-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/55f7be953b94/nihpp-2025.07.08.663727v2-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/3b9b0dabf1a9/nihpp-2025.07.08.663727v2-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/cb736bb6367b/nihpp-2025.07.08.663727v2-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957e/12320642/f768ea401849/nihpp-2025.07.08.663727v2-f0006.jpg

相似文献

1
Protection against reinfection with extends across heterologous Mtb lineages.针对不同分枝杆菌属结核杆菌谱系的再感染的保护作用广泛存在。
bioRxiv. 2025 Jul 31:2025.07.08.663727. doi: 10.1101/2025.07.08.663727.
2
TLR2 is non-redundant in the population and subpopulation responses to in macrophages and .TLR2 在巨噬细胞和 中的群体和亚群反应中是不可或缺的。
mSystems. 2023 Aug 31;8(4):e0005223. doi: 10.1128/msystems.00052-23. Epub 2023 Jul 13.
3
Diverse impacts of different rpoB mutations on the anti-tuberculosis efficacy of capreomycin.不同rpoB基因突变对卷曲霉素抗结核疗效的多样影响。
EBioMedicine. 2025 May 30;117:105776. doi: 10.1016/j.ebiom.2025.105776.
4
Xpert MTB/RIF Ultra assay for tuberculosis disease and rifampicin resistance in children.Xpert MTB/RIF Ultra assay 用于儿童结核病和利福平耐药检测。
Cochrane Database Syst Rev. 2022 Sep 6;9(9):CD013359. doi: 10.1002/14651858.CD013359.pub3.
5
Xpert® MTB/RIF assay for pulmonary tuberculosis and rifampicin resistance in adults.用于检测成人肺结核及利福平耐药性的Xpert® MTB/RIF检测法
Cochrane Database Syst Rev. 2014 Jan 21;2014(1):CD009593. doi: 10.1002/14651858.CD009593.pub3.
6
Xpert MTB/XDR for detection of pulmonary tuberculosis and resistance to isoniazid, fluoroquinolones, ethionamide, and amikacin.Xpert MTB/XDR 检测系统用于检测肺结核病及异烟肼、氟喹诺酮类、乙胺丁醇和阿米卡星耐药性。
Cochrane Database Syst Rev. 2022 May 18;5(5):CD014841. doi: 10.1002/14651858.CD014841.pub2.
7
Xpert MTB/RIF assay for extrapulmonary tuberculosis and rifampicin resistance.用于肺外结核病和利福平耐药性的Xpert MTB/RIF检测
Cochrane Database Syst Rev. 2018 Aug 27;8(8):CD012768. doi: 10.1002/14651858.CD012768.pub2.
8
South Asian origin and global transmission history of lineage 4.4 型谱系的南亚起源及全球传播史。
mSystems. 2025 Jun 17;10(6):e0042725. doi: 10.1128/msystems.00427-25. Epub 2025 May 20.
9
Immunogenicity, safety, and efficacy of the vaccine H56:IC31 in reducing the rate of tuberculosis disease recurrence in HIV-negative adults successfully treated for drug-susceptible pulmonary tuberculosis: a double-blind, randomised, placebo-controlled, phase 2b trial.疫苗H56:IC31在降低成功治疗药物敏感型肺结核的HIV阴性成人结核病复发率方面的免疫原性、安全性和疗效:一项双盲、随机、安慰剂对照的2b期试验。
Lancet Infect Dis. 2025 Jul;25(7):751-763. doi: 10.1016/S1473-3099(24)00814-4. Epub 2025 Mar 5.
10
Concurrent TB and HIV therapies effectively control clinical reactivation of TB during co-infection but fail to eliminate chronic immune activation.同时进行的结核病和艾滋病治疗能有效控制合并感染期间结核病的临床复发,但无法消除慢性免疫激活。
Res Sq. 2024 Aug 26:rs.3.rs-4908400. doi: 10.21203/rs.3.rs-4908400/v1.

本文引用的文献

1
Intravenous BCG-mediated protection against tuberculosis requires CD4+ T cells and CD8α+ lymphocytes.静脉注射卡介苗介导的抗结核保护作用需要CD4 + T细胞和CD8α +淋巴细胞。
J Exp Med. 2025 Apr 7;222(4). doi: 10.1084/jem.20241571. Epub 2025 Feb 6.
2
Engineered Mycobacterium tuberculosis triple-kill-switch strain provides controlled tuberculosis infection in animal models.工程化结核分枝杆菌三重杀灭开关菌株在动物模型中实现了对结核病感染的可控性。
Nat Microbiol. 2025 Feb;10(2):482-494. doi: 10.1038/s41564-024-01913-5. Epub 2025 Jan 10.
3
Paired analysis of host and pathogen genomes identifies determinants of human tuberculosis.
宿主和病原体基因组的配对分析确定了人类结核病的决定因素。
Nat Commun. 2024 Nov 29;15(1):10393. doi: 10.1038/s41467-024-54741-w.
4
CD4 T cells re-wire granuloma cellularity and regulatory networks to promote immunomodulation following Mtb reinfection.CD4 T 细胞重新构建肉芽肿细胞组成和调控网络,以促进 Mtb 再感染后的免疫调节。
Immunity. 2024 Oct 8;57(10):2380-2398.e6. doi: 10.1016/j.immuni.2024.08.002. Epub 2024 Aug 29.
5
Host and pathogen genetic diversity shape vaccine-mediated protection to .宿主和病原体遗传多样性塑造疫苗介导的 保护。
Front Immunol. 2024 Jun 28;15:1427846. doi: 10.3389/fimmu.2024.1427846. eCollection 2024.
6
Identification of bacterial determinants of tuberculosis infection and treatment outcomes: a phenogenomic analysis of clinical strains.结核感染和治疗结局的细菌决定因素鉴定:临床分离株的表型基因组分析。
Lancet Microbe. 2024 Jun;5(6):e570-e580. doi: 10.1016/S2666-5247(24)00022-3. Epub 2024 May 8.
7
Antibiotic treatment modestly reduces protection against reinfection in macaques.抗生素治疗在一定程度上降低了猕猴免受再感染的保护作用。
Infect Immun. 2024 Apr 9;92(4):e0053523. doi: 10.1128/iai.00535-23. Epub 2024 Mar 22.
8
Airway T cells are a correlate of i.v. Bacille Calmette-Guerin-mediated protection against tuberculosis in rhesus macaques.气道 T 细胞是猕猴静脉内接种卡介苗预防结核病的相关因素。
Cell Host Microbe. 2023 Jun 14;31(6):962-977.e8. doi: 10.1016/j.chom.2023.05.006. Epub 2023 Jun 1.
9
Response to Hypoxia and the Ensuing Dysregulation of Inflammation Impacts Pathogenicity.应对缺氧和随之而来的炎症失调会影响致病性。
Am J Respir Crit Care Med. 2022 Jul 1;206(1):94-104. doi: 10.1164/rccm.202112-2747OC.
10
Coordinated In Vitro Release of Granulysin, Perforin and IFN-γ in TB and HIV/TB Co-Infection Associated with Clinical Outcomes before and after Anti-TB Treatment.结核病及HIV/结核病合并感染中颗粒溶素、穿孔素和IFN-γ的体外协同释放与抗结核治疗前后临床结局的相关性
Pathogens. 2020 Aug 14;9(8):655. doi: 10.3390/pathogens9080655.