Evidence map›Paper›PMID 27009269›Full record

ArticleScience translational medicine2016

Arginase-1-dependent promotion of TH17 differentiation and disease progression by MDSCs in systemic lupus erythematosus.

Hao Wu, Yu Zhen, Zhanchuan Ma, Huimin Li, Jinyu Yu, Zhong-Gao Xu, Xiang-Yang Wang, Huanfa Yi, Yong-Guang Yang

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

117 citing papers in PubMed, 187 citations in OpenAlex.

  1. Review
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  5. Myeloid-Derived Suppressor Cells in Inflammatory Arthritis.International journal of molecular sciences · 2026
    Review
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57 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Hao WuThe First Hospital and Institute of Immunology, Jilin University, Changchun 130061, China.
Yu ZhenThe First Hospital and Institute of Immunology, Jilin University, Changchun 130061, China.
Zhanchuan MaThe First Hospital and Institute of Immunology, Jilin University, Changchun 130061, China.
Huimin LiThe First Hospital and Institute of Immunology, Jilin University, Changchun 130061, China.
Jinyu YuThe First Hospital and Institute of Immunology, Jilin University, Changchun 130061, China.
Zhong-Gao XuThe First Hospital and Institute of Immunology, Jilin University, Changchun 130061, China.
Xiang-Yang WangDepartment of Human and Molecular Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.
Huanfa YiThe First Hospital and Institute of Immunology, Jilin University, Changchun 130061, China. yihuanfa@jlu.edu.cn yy2324@columbia.edu.
Yong-Guang YangThe First Hospital and Institute of Immunology, Jilin University, Changchun 130061, China. Department of Medicine, Columbia Center for Translational Immunology, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA. yihuanfa@jlu.edu.cn yy2324@columbia.edu.
First Hospital of Jilin University · CNJilin University · CNVirginia Commonwealth University · US

Funding

Large heat shock proteins and their role in cancer therapyR01CA099326 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI REPASKY, ELIZABETH A, WANG, XIANG-YANG SHAWN · 2003 to 2020
$5.7M
Role of CD47 in xenograft rejection by macrophagesR01AI064569 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI YANG, YONG-GUANG · 2008 to 2016
$3.1M
Large Stress Proteins in Biology and MedicineR01CA154708 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI WANG, XIANG-YANG SHAWN · 2011 to 2015
$1.5M
Scavenger Receptor-A and Immune RegulationR01CA129111 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI WANG, XIANG-YANG SHAWN · 2007 to 2011
$1.2M
NCI NIH HHS R01 CA099326NCI NIH HHS R01 CA129111NCI NIH HHS R01 CA154708NIAID NIH HHS R01 AI064569
6 · The paper itself

Abstract

Expansion of myeloid-derived suppressor cells (MDSCs) has been documented in some murine models and patients with autoimmune diseases, but the exact role of MDSCs in this process remains largely unknown. The current study investigates this question in patients with systemic lupus erythematosus (SLE). Patients with active SLE showed a significant increase in HLA-DR(-)CD11b(+)CD33(+)MDSCs, including both CD14(+)CD66b(-)monocytic and CD14(-)CD66b(+)granulocytic MDSCs, in the peripheral blood compared to healthy controls (HCs). The frequency of MDSCs was positively correlated with the levels of serum arginase-1 (Arg-1) activity, T helper 17 (TH17) responses, and disease severity in SLE patients. Consistently, in comparison with MDSCs from HCs, MDSCs from SLE patients exhibited significantly elevated Arg-1 production and increased potential to promote TH17 differentiation in vitro in an Arg-1-dependent manner. Moreover, in a humanized SLE model, MDSCs were essential for the induction of TH17 responses and the associated renal injuries, and the effect of MDSCs was Arg-1-dependent. Our data provide direct evidence demonstrating a pathogenic role for MDSCs in human SLE. This study also provides a molecular mechanism of the pathogenesis of SLE by demonstrating an Arg-1-dependent effect of MDSCs in the development of TH17 cell-associated autoimmunity, and suggests that targeting MDSCs or Arg-1 may offer potential therapeutic strategies for the treatment of SLE and other TH17 cell-mediated autoimmune diseases.

Indexed as

Cell DifferentiationDisease ProgressionAnimalsArginaseCytokinesHumansLupus Erythematosus, SystemicLymphocyte CountMice, SCIDMyeloid-Derived Suppressor CellsProteinuriaTh17 CellsARG1 protein, humanArginaseCytokines

Identifiers

PMID27009269
PMCPMC4895207
OpenAlexW2304854632

What OpenQuestion holds

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LicenceTDM
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.