Evidence map›Paper›PMID 29669565›Full record

ArticleRespiratory research2018

Human alveolar macrophages predominately express combined classical M1 and M2 surface markers in steady state.

Elena Mitsi, Raphael Kamng'ona, Jamie Rylance, Carla Solórzano, J Jesus Reiné, Henry C Mwandumba, Daniela M Ferreira, Kondwani C Jambo

Abstract readLetter
In one paragraph

Article in Respiratory research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
–field-weighted citation impact
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

87 citing papers in PubMed.

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  9. Journal of animal science and technology · 2026
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27 more citing papers are in PubMed but not listed here.

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.

Elena MitsiDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Raphael Kamng'onaMalawi Liverpool Wellcome Trust Clinical Research Programme, College of Medicine, P.O Box 30096, Chichiri, Blantyre, 3, Malawi.
Jamie RylanceDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Carla SolórzanoDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
J Jesus ReinéDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Henry C MwandumbaDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Daniela M FerreiraDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Kondwani C JamboDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK. Kondwani.Jambo@lstmed.ac.uk.

Funding

Bill and Melinda Gates Foundation OPP1117728Medical Research Council MR/M011569/Medical Research Council MR/M011569/1Medical Research Council MR/P020526/1Wellcome Trust 105831/Z/14/Z
6 · The paper itself

Abstract

Alveolar macrophages (AM) are critical to the homeostasis of the inflammatory environment in the lung. Differential expression of surface markers classifies macrophages to either classically (M1) or alternatively activated (M2). We investigated the phenotype of human alveolar macrophages (AM) in adults living in two different geographical locations: UK and Malawi. We show that the majority of AM express high levels of M1 and M2 markers simultaneously, with the M1/M2 phenotype being stable in individuals from different geographical locations. The combined M1/M2 features confer to AM a hybrid phenotype, which does not fit the classic macrophage classification. This hybrid phenotype may confer to alveolar macrophages an ability to quickly switch between M1 or M2 associated functions allowing for appropriate responses to stimuli and tissue environment.

Indexed as

PhenotypeAdolescentAdultAntigens, CDBiomarkersCohort StudiesGene ExpressionHumansMacrophage ActivationMacrophages, AlveolarMiddle AgedUnited KingdomYoung AdultAntigens, CDBiomarkers

Identifiers

PMID29669565
PMCPMC5907303

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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.