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本文引用的文献

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B-Cell Epitope Mapping of the Tp0435 Immunodominant Lipoprotein for Peptide-Based Syphilis Diagnostics.用于基于肽的梅毒诊断的Tp0435免疫显性脂蛋白的B细胞表位图谱分析
Diagnostics (Basel). 2025 Jun 5;15(11):1443. doi: 10.3390/diagnostics15111443.
2
Resistance to ceftriaxone and penicillin G among contemporary syphilis strains confirmed by natural in vitro mutagenesis.当代梅毒菌株对头孢曲松和青霉素G的耐药性通过自然体外诱变得到证实。
Commun Med (Lond). 2025 Jun 10;5(1):224. doi: 10.1038/s43856-025-00948-x.
3
Protein TpF1 Inhibits Migration by Impairing Actin Polymerization via Toll-Like Receptor 4/PI3K/AKT in Microglia.蛋白TpF1通过Toll样受体4/PI3K/AKT损害小胶质细胞中的肌动蛋白聚合来抑制迁移。
ACS Infect Dis. 2025 May 9;11(5):1104-1113. doi: 10.1021/acsinfecdis.4c00868. Epub 2025 Apr 24.
4
A comprehensive strategy for the development of a multi-epitope vaccine targeting , utilizing heat shock proteins, encompassing the entire process from vaccine design to evaluation of immunogenicity.一种开发针对……的多表位疫苗的综合策略,利用热休克蛋白,涵盖从疫苗设计到免疫原性评估的整个过程。 (注:原文中“targeting”后缺少具体目标,翻译时保留原文状态)
Front Microbiol. 2025 Mar 19;16:1551437. doi: 10.3389/fmicb.2025.1551437. eCollection 2025.
5
The Significance of the Cell-Mediated Host Immune Response in Syphilis.细胞介导的宿主免疫反应在梅毒中的意义。
Microorganisms. 2024 Dec 13;12(12):2580. doi: 10.3390/microorganisms12122580.
6
Treponema Pallidum protein Tp47 triggers macrophage inflammatory senescence via PKM2-mediated metabolic reprogramming.梅毒螺旋体蛋白Tp47通过PKM2介导的代谢重编程触发巨噬细胞炎症衰老。
Int J Biol Macromol. 2024 Dec;283(Pt 4):137991. doi: 10.1016/j.ijbiomac.2024.137991. Epub 2024 Nov 22.
7
Global, regional, and national burden of syphilis, 1990-2021 and predictions by Bayesian age-period-cohort analysis: a systematic analysis for the global burden of disease study 2021.1990年至2021年梅毒的全球、区域和国家负担以及贝叶斯年龄-时期-队列分析预测:2021年全球疾病负担研究的系统分析
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8
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Blocking pathogenic Leptospira invasion with aptamer molecules targeting outer membrane LipL32 protein.利用针对外膜 LipL32 蛋白的适体分子阻断致病性钩端螺旋体的入侵。
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发病机制中的参与者:功能蛋白的进展。

Participants in pathogenesis: progress in functional proteins.

作者信息

Zuo Wei, Xiao Yongjian, Xiang Qing, Xiao Shuangwen, Xie Yafeng

机构信息

Department of Clinical Laboratory, The Second Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, China.

出版信息

Front Immunol. 2025 Aug 26;16:1632677. doi: 10.3389/fimmu.2025.1632677. eCollection 2025.

DOI:10.3389/fimmu.2025.1632677
PMID:40933996
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12417408/
Abstract

is the causative agent of syphilis, a chronic sexually transmitted disease that leads to widespread organ damage. The pathogenesis of syphilis involves crucial functional proteins that facilitate bacterial adhesion to host cells, invasion, dissemination, immune evasion, and inflammatory responses. Investigating these proteins is crucial for the development of innovative diagnostic tools, vaccines, and therapies. However, the intricate nature of and the inability to culture hinder our comprehensive understanding of these proteins. This review article presents innovative understandings of the pathogenesis of functional proteins, building upon existing knowledge. This paper establishes a foundation for comprehending the current knowledge landscape and outlining future research avenues.

摘要

是梅毒的病原体,梅毒是一种慢性性传播疾病,会导致广泛的器官损害。梅毒的发病机制涉及关键功能蛋白,这些蛋白有助于细菌粘附于宿主细胞、侵入、传播、免疫逃逸和炎症反应。研究这些蛋白对于开发创新的诊断工具、疫苗和治疗方法至关重要。然而,其复杂的性质以及无法培养的情况阻碍了我们对这些蛋白的全面理解。这篇综述文章在现有知识的基础上,对功能性蛋白的发病机制提出了创新性的理解。本文为理解当前的知识格局和勾勒未来的研究途径奠定了基础。

需注意,原文中部分关键内容缺失,比如缺失具体的病原体名称等,上述译文是在尽量按照正确逻辑翻译的基础上,根据现有内容补全以使译文完整。