Evidence map›Paper›PMID 34696391›Full record

ArticleViruses2021

Alveolar-like Macrophages Attenuate Respiratory Syncytial Virus Infection.

Bárbara N Porto, Michael L Litvack, Yuchen Cen, Irene Lok, Sheena Bouch, Michael J Norris, Wenming Duan, Cameron Ackerley, Martin Post, Theo J Moraes

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 8 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

10 authors at 3 institutions in 3 countries.

Bárbara N PortoProgram in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Michael L LitvackProgram in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.ORCID 0000-0001-9236-5493
Yuchen CenProgram in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Irene LokProgram in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Sheena BouchProgram in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Michael J NorrisProgram in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Wenming DuanProgram in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Cameron AckerleyProgram in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Martin PostProgram in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.ORCID 0000-0003-4258-9303
Theo J MoraesProgram in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.ORCID 0000-0001-9968-6601
Hospital for Sick Children · CAUniversity of Toronto · CALa Jolla Institute for Immunology · US

Funding

CIHR FND-143309
6 · The paper itself

Abstract

Respiratory Syncytial Virus (RSV) is the leading cause of acute lower respiratory infections in young children and infection has been linked to the development of persistent lung disease in the form of wheezing and asthma. Despite substantial research efforts, there are no RSV vaccines currently available and an effective monoclonal antibody targeting the RSV fusion protein (palivizumab) is of limited general use given the associated expense. Therefore, the development of novel approaches to prevent RSV infection is highly desirable to improve pediatric health globally. We have developed a method to generate alveolar-like macrophages (ALMs) from pluripotent stem cells. These ALMs have shown potential to promote airway innate immunity and tissue repair and so we hypothesized that ALMs could be used as a strategy to prevent RSV infection. Here, we demonstrate that ALMs are not productively infected by RSV and prevent the infection of epithelial cells. Prevention of epithelial infection was mediated by two different mechanisms: phagocytosis of RSV particles and release of an antiviral soluble factor different from type I interferon. Furthermore, intratracheal administration of ALMs protected mice from subsequent virus-induced weight loss and decreased lung viral titres and inflammation, indicating that ALMs can impair the pathogenesis of RSV infection. Our results support a prophylactic role for ALMs in the setting of RSV infection and warrant further studies on stem cell-derived ALMs as a novel cell-based therapy for pulmonary viral infections.

Indexed as

Immunity, InnateAnimalsAntibodies, ViralCell- and Tissue-Based TherapyCell LineEpithelial CellsFetal BloodHumansInflammationMacrophagesMacrophages, AlveolarMiceMice, Inbred BALB CPluripotent Stem CellsRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsAntibodies, Viralalveolar macrophagesrespiratory infectionRespiratory Syncytial Virusstem cells

Identifiers

PMID34696391
PMCPMC8540499
OpenAlexW3204748243

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.