Evidence map›Paper›PMID 38644444›Full record

ArticleScience China. Life sciences2024

High dimensional proteomic mapping of bone marrow immune characteristics in immune thrombocytopenia.

Feng-Qi Liu, Qing-Yuan Qu, Ying Lei, Qi Chen, Yu-Xiu Chen, Meng-Lin Li, Xue-Yan Sun, Ye-Jun Wu, Qiu-Sha Huang, Hai-Xia Fu and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Science China. Life sciences, 2024. 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
0.9field-weighted citation impact, top 25% of its field
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, 2 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
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

15 authors at 6 institutions in 2 countries.

Feng-Qi Liu *Peking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Qing-Yuan Qu *Peking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Ying LeiCAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, 100101, China.
Qi ChenPeking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Yu-Xiu ChenPeking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Meng-Lin LiPeking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Xue-Yan SunPeking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Ye-Jun WuPeking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Qiu-Sha HuangPeking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Hai-Xia FuPeking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Yuan KongPeking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Yue-Ying LiCAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, 100101, China.
Qian-Fei WangCAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, 100101, China.
Xiao-Jun HuangPeking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China.
Xiao-Hui ZhangPeking University People's Hospital, Peking University Institute of Hematology, Beijing, 100044, China. zhangxh@bjmu.edu.cn.
National Clinical Research Center for Digestive Diseases · CNPeking University People's Hospital · CNPeking University · CNBeijing Institute of Genomics · CNChinese Academy of Sciences · CNUniversity of Chinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the role of co-stimulatory and co-inhibitory molecules on immune tolerance in immune thrombocytopenia (ITP), this study mapped the immune cell heterogeneity in the bone marrow of ITP at the single-cell level using Cytometry by Time of Flight (CyTOF). Thirty-six patients with ITP and nine healthy volunteers were enrolled in the study. As soluble immunomodulatory molecules, more sCD25 and sGalectin-9 were detected in ITP patients. On the cell surface, co-stimulatory molecules like ICOS and HVEM were observed to be upregulated in mainly central memory and effector T cells. In contrast, co-inhibitory molecules such as CTLA-4 were significantly reduced in Th1 and Th17 cell subsets. Taking a platelet count of 30×10

Indexed as

Bone MarrowProteomicsPurpura, Thrombocytopenic, IdiopathicAdultAgedFemaleHumansMaleMiddle AgedPlatelet CountYoung Adultautoimmune diseasesbone marrowco-inhibitoryco-stimulatoryCTLA4Cytometry by Time of Flightimmune checkpointimmune thrombocytopenia

Identifiers

PMID38644444
OpenAlexW4395007266

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.