Evidence map›Paper›PMID 30897137›Full record

ArticlePloS one2019

Comparative proteomic study reveals the enhanced immune response with the blockade of interleukin 10 with anti-IL-10 and anti-IL-10 receptor antibodies in human U937 cells.

Guoying Ni, Shu Chen, Jianwei Yuan, Shelley F Cavezza, Ming Q Wei, Hejie Li, Xuan Pan, Xiaosong Liu, Tianfang Wang

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

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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

9 authors at 5 institutions in 3 countries.

Guoying NiThe First Affiliated Hospital/School of Clinical Medicine of Guangdong Pharmaceutical University, Guangzhou, China.
Shu ChenCancer Research Institute, First People's Hospital of Foshan, Foshan, Guangdong, China.
Jianwei YuanThe First Affiliated Hospital/School of Clinical Medicine of Guangdong Pharmaceutical University, Guangzhou, China.
Shelley F CavezzaSchool of Health and Sport Sciences, University of the Sunshine Coast, Maroochydore DC, Australia.ORCID 0000-0002-5857-6913
Ming Q WeiSchool of Medical Science, Griffith Health Institute, Griffith University, Gold Coast, Australia.
Hejie LiInstitute of Industrial Science, Department of Mechanical and Bio-functional System, the University of Tokyo, Tokyo, Japan.
Xuan PanThe First Affiliated Hospital/School of Clinical Medicine of Guangdong Pharmaceutical University, Guangzhou, China.
Xiaosong LiuThe First Affiliated Hospital/School of Clinical Medicine of Guangdong Pharmaceutical University, Guangzhou, China.
Tianfang WangGenecology Research Centre, University of the Sunshine Coast, Maroochydore DC, Australia.ORCID 0000-0002-4876-7767
University of the Sunshine Coast · AUGriffith University · AUGuangdong Pharmaceutical University · CNFirst People's Hospital of Foshan · CNThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blocking cytokine interleukin 10 (IL-10) at the time of immunisation enhances vaccine induced T cell responses and improves control of tumour cell growth in vivo. However, the effect of an IL-10 blockade on the biological function of macrophages has not been explored. In the current paper, a macrophage precursor cell line, U937 cells, was selected to investigate the differential expression of proteins and relevant cell signalling pathway changes, when stimulated with lipopolysaccharide (LPS) in the presence of antibodies to IL-10 or IL-10 receptor. We used a quantitative proteomic strategy to investigate variations in protein profiles of U937 cells following the treatments with LPS, LPS plus human anti-IL10 antibody and anti-IL10R antibody in 24hrs, respectively. The LPS treatment significantly activated actin-related cell matrix formation and immune response pathways. The addition of anti-IL10 and anti-IL10R antibody further promoted the immune response and potentially effect macrophage survival through PI3K/AKT signalling; however, the latter appeared to also upregulated oncogene XRCC5 and Cajal body associated processes.

Indexed as

Antibodies, MonoclonalCell ProliferationGene Expression RegulationHumansInterleukin-10MacrophagesProtein Interaction MapsProteomeProteomicsReceptors, Interleukin-10Signal TransductionU937 CellsAntibodies, MonoclonalIL10 protein, humanInterleukin-10ProteomeReceptors, Interleukin-10

Identifiers

PMID30897137
PMCPMC6428271
OpenAlexW2922723823

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Registered trials

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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.