Evidence map›Paper›PMID 36263841›Full record

ArticleHaematologica2023

Enhancing regulatory T-cell function via inhibition of high mobility group box 1 protein signaling in immune thrombocytopenia.

Haoyi Wang, Tianshu Yu, Ning An, Yunqi Sun, Pengcheng Xu, Panpan Han, Yajing Zhao, Lingjun Wang, Xiaofei Ni, Yubin Li and 5 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

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  7. Baohe Pingwei power plus neoadjuvant chemotherapy for gastric cancer.World journal of gastrointestinal surgery · 2025
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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 2 institutions in 2 countries.

Haoyi WangDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Tianshu YuDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Ning AnLaboratory of Cancer Signaling, Interdisciplinary Cluster for Applied Genoproteomics (GIGA) Stem Cells, University of Liège, CHU, Sart-Tilman, Liège, 4000 Belgium.
Yunqi SunDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Pengcheng XuDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Panpan HanDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Yajing ZhaoDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Lingjun WangDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Xiaofei NiDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Yubin LiDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Guosheng LiDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Yanfeng LiuDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Jun PengDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012.
Ming HouDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012, China; Shandong Provincial Key Laboratory of Immunohematology, Qilu Hospital of Shandong University, Jinan. qlhouming@sina.com.
Yu HouDepartment of Hematology, Qilu Hospital of Shandong University, Shandong University, Jinan, Shandong, 250012, China; Shandong Provincial Key Laboratory of Immunohematology, Qilu Hospital of Shandong University, Jinan. houyu2009@sina.com.
Qilu Hospital of Shandong University · CNUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary immune thrombocytopenia (ITP) is the most common acquired autoimmune bleeding disorder. Abnormally increased levels of High Mobility Group Box 1 (HMGB1) protein associate with thrombocytopenia and therapeutic outcome in ITP. Previous studies proposed that a natural inhibitor of HMGB1, 18β-glycyrrhetinic acid (18β-GA), could be used for its anti-inflammatory and immune-modulatory effects, although its ability to correct immune balance in ITP is unclear. In this study, we showed that plasma HMGB1 correlated negatively with platelet counts in ITP patients, and confirmed that 18β-GA stimulated the production of regulatory T cells (Treg), restored the balance of CD4+ T-cell subsets and enhanced the suppressive function of Treg through blocking the effect on HMGB1 in patients with ITP. HMGB1 short hairpin RNA interference masked the effect of 18β-GA in Treg of ITP patients. Furthermore, we found that 18β-GA alleviated thrombocytopenia in mice with ITP. Briefly, anti-CD61 immune-sensitized splenocytes were transferred into severe combined immunodeficient mice to induce a murine model of severe ITP. The proportion of circulating Treg increased significantly, while the level of plasma HMGB1 and serum antiplatelet antibodies decreased significantly in ITP mice along 18β-GA treatment. In addition, 18β-GA reduced phagocytic activity of macrophages towards platelets both in ITP patients and ITP mice. These results indicate that 18β-GA has the potential to restore immune balance in ITP via inhibition of HMGB1 signaling. In short, this study reveals the role of HMGB1 in ITP, which may serve as a potential target for thrombocytopenia therapy.

Indexed as

HMGB1 ProteinPurpura, Thrombocytopenic, IdiopathicThrombocytopeniaAnimalsGlycyrrhetinic AcidMiceT-Lymphocytes, Regulatory18alpha-glycyrrhetinic acidGlycyrrhetinic AcidHMGB1 Protein

Identifiers

PMID36263841
PMCPMC9973480
OpenAlexW4306868160

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.