Evidence map›Paper›PMID 40853519›Full record

ArticleAMB Express2025

Treponema pallidum inhibits CD4+ T-cell proliferation through METAP2: insights from Mendelian randomization analysis.

Zhaoping Liu, Xiaohong Zhang, Ting Lin, Xuan Ding, Han Yu, Jiangchen Yao, Ke Gao, Yimou Wu, Feijun Zhao

Abstract read
In one paragraph

Article in AMB Express, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Infection and immunity · 2026
    Review
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Zhaoping Liu *Department of Clinical Laboratory Medicine, Institution of Microbiology and Infectious Diseases, Hunan Province Clinical Research Center for Accurate Diagnosis and Treatment of High-incidence Sexually Transmitted Diseases, The First Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan, People's Republic of China.
Xiaohong Zhang *MOE Key Lab of Rare Pediatric Diseases&Institute of Pathogenic Biology and Key Laboratory of Special Pathogen Prevention and Control of Hunan Province, Hengyang Medical College, University of South China, Hengyang City, 421001, People's Republic of China.
Ting Lin *School of Public Health, Hengyang Medical School, University of South China, Hengyang, 421001, People's Republic of China.
Xuan DingMOE Key Lab of Rare Pediatric Diseases&Institute of Pathogenic Biology and Key Laboratory of Special Pathogen Prevention and Control of Hunan Province, Hengyang Medical College, University of South China, Hengyang City, 421001, People's Republic of China.
Han YuMOE Key Lab of Rare Pediatric Diseases&Institute of Pathogenic Biology and Key Laboratory of Special Pathogen Prevention and Control of Hunan Province, Hengyang Medical College, University of South China, Hengyang City, 421001, People's Republic of China.
Jiangchen YaoMOE Key Lab of Rare Pediatric Diseases&Institute of Pathogenic Biology and Key Laboratory of Special Pathogen Prevention and Control of Hunan Province, Hengyang Medical College, University of South China, Hengyang City, 421001, People's Republic of China.
Ke GaoMOE Key Lab of Rare Pediatric Diseases&Institute of Pathogenic Biology and Key Laboratory of Special Pathogen Prevention and Control of Hunan Province, Hengyang Medical College, University of South China, Hengyang City, 421001, People's Republic of China.
Yimou WuMOE Key Lab of Rare Pediatric Diseases&Institute of Pathogenic Biology and Key Laboratory of Special Pathogen Prevention and Control of Hunan Province, Hengyang Medical College, University of South China, Hengyang City, 421001, People's Republic of China. yimouwu@sina.com.
Feijun ZhaoMOE Key Lab of Rare Pediatric Diseases&Institute of Pathogenic Biology and Key Laboratory of Special Pathogen Prevention and Control of Hunan Province, Hengyang Medical College, University of South China, Hengyang City, 421001, People's Republic of China. nhdxzhfj@163.com.

Funding

Health High-Level Talents Major Scientific Research Project of Hunan Provincial Health Commission R2023004Health Research Key Project of Hunan Provincial Health Commission no. 20221064723Hunan Province Natural Science Foundation 2024JJ5343Hunan Province Natural Science Foundation no. 2023JJ30530Major Scientific and Technological Projects for collaborative prevention and control of birth defects in Hunan Province no. 2019SK1010Research funding of the First Affiliated Hospital of University of South China no. 20230005-1015Scientific Research and Innovation Project of postgraduates in Hunan Province no. CX20220974the National Natural Science Foundation of China no. 81971980
6 · The paper itself

Abstract

Neurosyphilis (NS) is a chronic central nervous system infection caused by Treponema pallidum. Owing to its diverse clinical manifestations and the limited sensitivity of current diagnostic methods, NS is difficult to diagnose. Understanding the molecular mechanisms of NS and identifying reliable biomarkers are essential for improving diagnostic and therapeutic strategies. This study employed Mendelian randomization (MR) analysis to explore the causal relationships among protein ratio quantitative trait loci (rQTLs), cerebrospinal fluid (CSF) metabolites, and syphilis risk at various stages. The results revealed that several rQTLs, including CD46/TNFRSF14 and TBC1D23/TBC1D5, were closely associated with syphilis risk, whereas others, such as BANK1/HEXIM1 and GOPC/HEXIM1, exhibited protective effects. Mediation analysis further identified key CSF metabolites, such as N-acetyltaurine and bilirubin, as important mediators linking rQTLs and syphilis progression. Through integrated analysis of cis-proteins from rQTLs and transcriptomic data from CD4 + T-cells of NS patients, METAP2 was identified as a key biomarker in NS, with the potential mechanisms elucidated. Importantly, T. pallidum may inhibit CD4 + T-cell proliferation by modulating METAP2, thereby accelerating disease progression. These findings offer new insights into the pathogenesis of NS and highlight METAP2 as a potential biomarker, laying a foundation for improving diagnostic and therapeutic strategies.

Indexed as

CD4 + T-cellsCerebrospinal fluid metabolitesMendelian randomizationMETAP2Treponema pallidum

Identifiers

PMID40853519
PMCPMC12379665

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.