Evidence map›Paper›PMID 34378952›Full record

ArticleMicrobiology spectrum2021

SARS-CoV-2 Isolates Show Impaired Replication in Human Immune Cells but Differential Ability to Replicate and Induce Innate Immunity in Lung Epithelial Cells.

Miao Jiang, Pekka Kolehmainen, Laura Kakkola, Sari Maljanen, Krister Melén, Teemu Smura, Ilkka Julkunen, Pamela Österlund

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 20 citations in OpenAlex.

  1. Extra gene coding capacity of SARS-CoV-2 provides a virus engineering platform for in vitro and in vivo applications.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Review
  3. Abortive infection of bat fibroblasts with SARS-CoV-2.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Interactions of SARS-CoV-2 with Human Target Cells-A Metabolic View.International journal of molecular sciences · 2024
    Review
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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.

Miao JiangExpert Microbiology Unit, Department of Health Security, Finnish Institute for Health and Welfare, Helsinki, Finland.ORCID 0000-0002-0733-7752
Pekka KolehmainenInfection and Immunity, Institute of Biomedicine, University of Turkugrid.1374.1, Turku, Finland.
Laura KakkolaInfection and Immunity, Institute of Biomedicine, University of Turkugrid.1374.1, Turku, Finland.
Sari MaljanenInfection and Immunity, Institute of Biomedicine, University of Turkugrid.1374.1, Turku, Finland.
Krister MelénExpert Microbiology Unit, Department of Health Security, Finnish Institute for Health and Welfare, Helsinki, Finland.
Teemu SmuraMedicum, Department of Virology, University of Helsinkigrid.7737.4, Helsinki, Finland.
Ilkka JulkunenInfection and Immunity, Institute of Biomedicine, University of Turkugrid.1374.1, Turku, Finland.
Pamela ÖsterlundExpert Microbiology Unit, Department of Health Security, Finnish Institute for Health and Welfare, Helsinki, Finland.ORCID 0000-0002-2229-6661
University of Turku · FIFinnish Institute for Health and Welfare · FIUniversity of Helsinki · FI

Funding

Academy of Finland (Suomen Akatemia) 297329Sigrid Juséliuksen Säätiö (Sigrid Jusélius Stiftelse)
6 · The paper itself

Abstract

The primary target organ of coronavirus disease 2019 (COVID-19) infection is the respiratory tract. Currently, there is limited information on the ability of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to infect and regulate innate immunity in human immune cells and lung epithelial cells. Here, we compared the ability of four Finnish isolates of SARS-CoV-2 from COVID-19 patients to replicate and induce interferons (IFNs) and other cytokines in different human cells. All isolates failed to replicate in dendritic cells, macrophages, monocytes, and lymphocytes, and no induction of cytokine gene expression was seen. However, most of the isolates replicated in Calu-3 cells, and they readily induced type I and type III IFN gene expression. The hCoV-19/Finland/FIN-25/2020 isolate, originating from a traveler from Milan in March 2020, showed better ability to replicate and induce IFN and inflammatory responses in Calu-3 cells than other isolates of SARS-CoV-2. Our data increase the knowledge on the pathogenesis and antiviral mechanisms of SARS-CoV-2 infection in human cell systems.

Indexed as

Immunity, InnateAngiotensin-Converting Enzyme 2Antiviral AgentsCOVID-19CytokinesEpithelial CellsGene ExpressionHumansInterferon LambdaInterferonsInterferon Type IKineticsLungPhylogenyRNA, ViralSARS-CoV-2ACE2 protein, humanAngiotensin-Converting Enzyme 2Antiviral AgentsCytokinesInterferon LambdaInterferonsInterferon Type IRNA, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2TrypsinCalu-3 cellCOVID-19human DChuman macrophageinterferon (IFN) responseSARS-CoV-2TPCK-treated trypsinVero E6 cellviral replication

Identifiers

PMID34378952
PMCPMC8552721
OpenAlexW3189330279

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.