Evidence map›Paper›PMID 25634246›Full record

ArticleStem cell research & therapy2015

Amnion cell-mediated immune modulation following bleomycin challenge: controlling the regulatory T cell response.

Jean L Tan, Siow T Chan, Camden Y Lo, James A Deane, Courtney A McDonald, Claude Ca Bernard, Euan M Wallace, Rebecca Lim

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
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  12. Biological properties and surgical applications of the human amniotic membrane.Frontiers in bioengineering and biotechnology · 2022
    Review
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  14. A protocol for cell therapy infusion in neonates.Stem cells translational medicine · 2021
    Article
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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

8 authors at 3 institutions in 1 country.

Jean L TanThe Ritchie Centre, Monash Institute of Medical Research, Monash University, 27-31 Wright St, Clayton, Victoria, 3168, Australia. jean.tan@monash.edu.
Siow T ChanThe Ritchie Centre, Monash Institute of Medical Research, Monash University, 27-31 Wright St, Clayton, Victoria, 3168, Australia. siow.chan@monash.edu.
Camden Y LoMonash Micro Imaging, Monash University, 27-31 Wright St, Clayton, Victoria, 3168, Australia. camden.low@monash.edu.
James A DeaneThe Ritchie Centre, Monash Institute of Medical Research, Monash University, 27-31 Wright St, Clayton, Victoria, 3168, Australia. james.deane@monash.edu.
Courtney A McDonaldThe Ritchie Centre, Monash Institute of Medical Research, Monash University, 27-31 Wright St, Clayton, Victoria, 3168, Australia. courtney.mcdonald@monash.edu.
Claude Ca BernardAustralian Regenerative Medicine Institute, Building 75, Wellington Rd, Clayton, Victoria, 3168, Australia. claude.bernard@monash.edu.
Euan M WallaceThe Ritchie Centre, Monash Institute of Medical Research, Monash University, 27-31 Wright St, Clayton, Victoria, 3168, Australia. euan.wallace@monash.edu.
Rebecca LimThe Ritchie Centre, Monash Institute of Medical Research, Monash University, 27-31 Wright St, Clayton, Victoria, 3168, Australia. rebecca.lim@monash.edu.
Monash University · AUMonash Institute of Medical Research · AUAustralian Regenerative Medicine Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe immunomodulatory properties of human amnion epithelial cells (hAECs) have been previously described in several disease models. We previously reported on the ability of hAECs to influence macrophage phenotype and chemotaxis. In this study, we aim to elucidate the contribution of regulatory T cells (Tregs) to macrophage polarisation and downstream effects on inflammation and fibrosis in a bleomycin model of lung injury.

methodsEither CD45(+)/FoxP3(+) Tregs or CD45(+)/FoxP3 (-) non-Tregs were adoptively transferred into Rag1 (-/-) mice immediately prior to bleomycin challenge. Four million hAECs were administered 24 hours later. Outcomes were measured 7 or 14 days later.

resultsMitigation of lung inflammation and fibrosis was observed only in animals that received both hAECs and Tregs. hAEC treatment also induced the maturation of non-Tregs into FoxP3-expressing Tregs. This event was found to be transforming growth factor-beta (TGFβ)-dependent. Furthermore, polarisation of macrophages from M1 to M2 occurred only in animals that received hAECs and Tregs.

conclusionsThis study provides the first evidence that Tregs are required for hAEC-mediated macrophage polarisation and consequential mitigation of bleomycin-induced lung injury. Uncovering the interactions between hAECs, macrophages, and T-cell subsets is central to understanding the mechanisms by which hAECs elicit lung repair.

Indexed as

AmnionAnimalsBleomycinCell DifferentiationCells, CulturedCoculture TechniquesDisease Models, AnimalEpithelial CellsFibrosisForkhead Transcription FactorsHomeodomain ProteinsInflammationLeukocyte Common AntigensLungLung InjuryMacrophagesBleomycinForkhead Transcription FactorsFOXP3 protein, humanHomeodomain ProteinsLeukocyte Common AntigensPTPRC protein, humanRAG-1 proteinTransforming Growth Factor beta

Identifiers

PMID25634246
PMCPMC4417266
OpenAlexW2157132853

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.