Evidence map›Paper›PMID 40755012›Full record

ArticleAnnals of medicine2025

Immune checkpoint changes correlate with the progression and prognosis of amyotrophic lateral sclerosis.

Sheng Chen, Chunzuan Xu, Changyun Liu, Jiaqi Li, Shupei Ke, Yingqian Lu, Yali Huang, Jialin Chen, Feifei Lin, Huapin Huang and 1 more

Abstract read
In one paragraph

Article in Annals of medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. ERVK activity in CD8Journal of neuroinflammation · 2026
    Article
  2. 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

11 authors.

Sheng ChenDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.ORCID 0000-0002-7934-015X
Chunzuan XuDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.ORCID 0009-0003-1186-4971
Changyun LiuDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
Jiaqi LiDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
Shupei KeDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
Yingqian LuDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
Yali HuangDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
Jialin ChenDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
Feifei LinDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
Huapin HuangDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
Zhangyu ZouDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.ORCID 0000-0002-8277-1110

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmyotrophic lateral sclerosis (ALS) urgently requires robust biomarkers for early diagnosis and prognostic stratification. This study aims to investigate the diagnostic and prognostic potential of membrane-bound and soluble immune checkpoint molecules in ALS pathogenesis.

methodsIn the present study at Fujian Medical Union Hospital, 72 participants (46 ALS and 26 healthy controls [HC]) underwent flow cytometry analysis of PD-1 expression in CD4

resultsFlow cytometry revealed elevated PD1 expression in CD4

conclusionsOur research demonstrated a considerable increase in membrane-bound and soluble PD-1 in ALS patients, correlating with disease progression and worse prognosis. Furthermore, we explored 13 other immune checkpoint molecules. Collectively, these molecules may be implicated in peripheral immune mechanisms underlying ALS pathogenesis. While baseline PD-1 levels show some association with prognosis, their elevation potentially indicates an unfavorable course.

Indexed as

Amyotrophic Lateral SclerosisImmune Checkpoint ProteinsProgrammed Cell Death 1 ReceptorAdultAgedBiomarkersCase-Control StudiesCD4-Positive T-LymphocytesDisease ProgressionFemaleFlow CytometryHumansMaleMiddle AgedNeurofilament ProteinsPrognosisBiomarkersImmune Checkpoint Proteinsneurofilament protein LNeurofilament ProteinsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorAmyotrophic lateral sclerosisimmune checkpointsPD-1prognosis

Identifiers

PMID40755012
PMCPMC12322990

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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.