Evidence map›Paper›PMID 27147271›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2016

The effect of immunosuppressive drug cyclosporine A on myeloid-derived suppressor cells in transplanted mice.

Chenlu Han, Tingting Wu, Ning Na, Yang Zhao, Weiguo Li, Yong Zhao

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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

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  10. Adoptive transfer of IFN-γ-induced M-MDSCs promotes immune tolerance to allografts through iNOS pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2019
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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

6 authors at 4 institutions in 1 country.

Chenlu HanCollege of Life Science, Henan Normal University, Xinxiang, Henan, China.
Tingting WuCollege of Life Science, Henan Normal University, Xinxiang, Henan, China.
Ning NaDepartment of Kidney Transplantation, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Yang ZhaoCollege of Life Science, Henan Normal University, Xinxiang, Henan, China.
Weiguo LiTransplantation Biology Research Division, State Key Laboratory of Membrane Biology, Institute of Zoology, Chinese Academy of Sciences, Beichen West Road 1-5, Chaoyang District, 100101, Beijing, China. liwg0618@htu.cn.
Yong ZhaoCollege of Life Science, Henan Normal University, Xinxiang, Henan, China. zhaoy@ioz.ac.cn.
Henan Normal University · CNChinese Academy of Sciences · CNInstitute of Zoology · CNThird Affiliated Hospital of Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveMyeloid-derived suppressor cells (MDSCs) play important roles in preventing graft rejection. Immunosuppressive drug cyclosporine A (CsA) is widely used in clinics to treat patients with allografts and autoimmune diseases. However, the effect of CsA on CD11b(+)Gr1(+) MDSCs has not been studied. SUBJECTS: The subjects of the study include BALB/c skin-grafted C57BL/6 mice and the in vitro MDSCs induction system. TREATMENT: Skin-grafted mice were treated with CsA (30 mg/kg, i.p.) or control buffer daily. 0.01 μg/ml CsA was added during MDSC induction.

methodsFlow cytometry was used to check cell phenotypes and proliferation. Real-time PCR was used for gene expressions. Inducible nitric oxide synthase iNOS-knockout mice were used for the role of iNOS in the immunosuppression of MDSCs.

resultsCsA in MDSC-induction system significantly increased the number of CD11b(+)Gr1(+)MDSCs without detectable effects on the expressions of CD31, CD115 and CD274. However, GM-CSF + CsA-induced MDSCs express higher iNOS than control MDSCs. Blocking iNOS activity by inhibitor or gene deletion significantly reversed the inhibitory effects of GM-CSF + CsA-induced MDSCs on T cell proliferation. Importantly, CsA treatment significantly increased the number and the immunosuppressive ability of CD11b(+)Gr1(+)MDSCs in allogeneic skin-grafted mice.

conclusionsCsA promotes MDSC induction and immunosuppressive function, which might be of clinical importance in treating graft rejection and autoimmune diseases.

Indexed as

Skin TransplantationAnimalsCell DifferentiationCell ProliferationCyclosporineImmunosuppressive AgentsMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutMyeloid-Derived Suppressor CellsNitric OxideNitric Oxide Synthase Type IIT-LymphocytesCyclosporineImmunosuppressive AgentsNitric OxideNitric Oxide Synthase Type IINos2 protein, mouseGraft rejectionImmune toleranceInnate immunityMyeloid-derived suppressor cells

Identifiers

PMID27147271
OpenAlexW2347082408

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.