Evidence map›Paper›PMID 36334153›Full record

ArticleCellular and molecular life sciences : CMLS2022

Induction of pulmonary HLA-G expression by SARS-CoV-2 infection.

Barbara Seliger, Simon Jasinski-Bergner, Chiara Massa, Anja Mueller, Katharina Biehl, Bo Yang, Michael Bachmann, Danny Jonigk, Philip Eichhorn, Arndt Hartmann and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. 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
1.2field-weighted citation impact, top 22% 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, 14 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

12 authors at 5 institutions in 1 country.

Barbara SeligerInstitute of Medical Immunology, Martin Luther University Halle-Wittenberg, Magdeburger Str. 2, 06112, Halle (Saale), Germany. immunologie@uk-halle.de.ORCID http://orcid.org/0000-0002-5544-4958
Simon Jasinski-BergnerInstitute of Medical Immunology, Martin Luther University Halle-Wittenberg, Magdeburger Str. 2, 06112, Halle (Saale), Germany.
Chiara MassaInstitute of Medical Immunology, Martin Luther University Halle-Wittenberg, Magdeburger Str. 2, 06112, Halle (Saale), Germany.
Anja MuellerInstitute of Medical Immunology, Martin Luther University Halle-Wittenberg, Magdeburger Str. 2, 06112, Halle (Saale), Germany.
Katharina BiehlInstitute of Medical Immunology, Martin Luther University Halle-Wittenberg, Magdeburger Str. 2, 06112, Halle (Saale), Germany.
Bo YangInstitute of Medical Immunology, Martin Luther University Halle-Wittenberg, Magdeburger Str. 2, 06112, Halle (Saale), Germany.
Michael BachmannHelmholtz Zentrum Dresden-Rossendorf (HZDR), Institute of Radiopharmaceutical Cancer Research, Dresden, Germany.
Danny JonigkInstitute of Pathology, Hannover Medical School, 30625, Hannover, Germany.
Philip EichhornInstitute of Pathology, Friedrich-Alexander University, 91054, Erlangen, Germany.
Arndt HartmannInstitute of Pathology, Friedrich-Alexander University, 91054, Erlangen, Germany.
Claudia WickenhauserInstitute of Pathology, Martin Luther University Halle-Wittenberg, 06112, Halle (Saale), Germany.
Marcus BauerInstitute of Pathology, Martin Luther University Halle-Wittenberg, 06112, Halle (Saale), Germany.
Martin Luther University Halle-Wittenberg · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEFraunhofer Institute for Cell Therapy and Immunology · DEHelmholtz-Zentrum Dresden-Rossendorf · DEMedizinische Hochschule Hannover · DE

Funding

Deutsche Forschungsgemeinschaft 496182670Deutsche Forschungsgemeinschaft JA 3192/1-1National University Medicine (NUM) network 01KX2121
6 · The paper itself

Abstract

The non-classical human leukocyte antigen (HLA)-G exerts immune-suppressive properties modulating both NK and T cell responses. While it is physiologically expressed at the maternal-fetal interface and in immune-privileged organs, HLA-G expression is found in tumors and in virus-infected cells. So far, there exists little information about the role of HLA-G and its interplay with immune cells in biopsies, surgical specimen or autopsy tissues of lung, kidney and/or heart muscle from SARS-CoV-2-infected patients compared to control tissues. Heterogeneous, but higher HLA-G protein expression levels were detected in lung alveolar epithelial cells of SARS-CoV-2-infected patients compared to lung epithelial cells from influenza-infected patients, but not in other organs or lung epithelia from non-viral-infected patients, which was not accompanied by high levels of SARS-CoV-2 nucleocapsid antigen and spike protein, but inversely correlated to the HLA-G-specific miRNA expression. High HLA-G expression levels not only in SARS-CoV-2-, but also in influenza-infected lung tissues were associated with a high frequency of tissue-infiltrating immune cells, but low numbers of CD8

Indexed as

COVID-19Influenza, HumanHLA-G AntigensHumansLungSARS-CoV-2HLA-G AntigensHLA-GImmune cell infiltrationImmune responsemicroRNASARS-CoV-2

Identifiers

PMID36334153
PMCPMC9637071
OpenAlexW4308312668

What OpenQuestion holds

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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.