A Study on the Inflammatory Response of the Brain in Neurosyphilis

Neurosyphilis (NS) is a clinical condition caused by infection of the central nervous system (CNS) by Treponema pallidum (Tp) that can lead to asymptomatic meningitis and more serious neurological diseases, such as dementia and blindness. However, current studies on the pathogenesis of NS are limited. Here, through the integration analysis of proteomics and single-cell transcriptomics, Toll-like/NF-κB signaling is identified as the key pathway involved in CNS damage caused by Tp. Moreover, monocyte-derived macrophages are key cells involved in the inflammatory response to Tp in the CNS of NS patients. In addition, it is found that inflammatory cells in peripheral blood may cause neurological damage through disruption of the blood‒brain barrier (BBB) in individuals with NS. Notably, activation of the Toll-like/NF-κB signaling pathway, as well as dysregulation of neural function, is likewise validated in an in vitro NS brain organoid model. In conclusion, the results revealed the mechanisms of inflammation-mediated brain injury in Tp-induced NS and provided new ideas for the clinical treatment of Tp infection.

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Publication Details

Journal
Advanced Science
Published
2024-11-22
DOI
https://doi.org/10.1002/advs.202406971
Citations
11
Primary Topic
Syphilis Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
3.59

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article

A Study on the Inflammatory Response of the Brain in Neurosyphilis

Qiyu Zhang, Ling Leng, Hanlin Zhang, Mansheng Li et al.
11 citations
Advanced Science
Syphilis Diagnosis and Treatment
3.59
article

A Study on the Inflammatory Response of the Brain in Neurosyphilis

Qiyu Zhang, Ling Leng, Hanlin Zhang, Mansheng Li, Jie Ma, Huizi Gong, Yujie Wang, Jun Li, Heyi Zheng, Jia Zhou
article en
11 citations

Abstract

Neurosyphilis (NS) is a clinical condition caused by infection of the central nervous system (CNS) by Treponema pallidum (Tp) that can lead to asymptomatic meningitis and more serious neurological diseases, such as dementia and blindness. However, current studies on the pathogenesis of NS are limited. Here, through the integration analysis of proteomics and single-cell transcriptomics, Toll-like/NF-κB signaling is identified as the key pathway involved in CNS damage caused by Tp. Moreover, monocyte-derived macrophages are key cells involved in the inflammatory response to Tp in the CNS of NS patients. In addition, it is found that inflammatory cells in peripheral blood may cause neurological damage through disruption of the blood‒brain barrier (BBB) in individuals with NS. Notably, activation of the Toll-like/NF-κB signaling pathway, as well as dysregulation of neural function, is likewise validated in an in vitro NS brain organoid model. In conclusion, the results revealed the mechanisms of inflammation-mediated brain injury in Tp-induced NS and provided new ideas for the clinical treatment of Tp infection.

Advanced ScienceVol. 12(5)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking Union Medical College Hospital (CN), Beijing Proteome Research Center (CN)
National Natural Science Foundation of China, Peking Union Medical College Hospital, Peking Union Medical College
Good health and well-being
Openalex Percentile: Top 6%
Syphilis Diagnosis and Treatment
3.59
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