Evidence map›Paper›PMID 33123167›Full record

Observational studyFrontiers in immunology2020

Pro- and Anti-Inflammatory Responses in Severe COVID-19-Induced Acute Respiratory Distress Syndrome-An Observational Pilot Study.

Quirin Notz, Marc Schmalzing, Florian Wedekink, Tobias Schlesinger, Michael Gernert, Johannes Herrmann, Lena Sorger, Dirk Weismann, Benedikt Schmid, Magdalena Sitter and 5 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 2 pooled it
6.9field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 2 syntheses or guidelines pooled it, 105 citations in OpenAlex.

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  11. Macrophages as a Source and Target of GDF-15.International journal of molecular sciences · 2024
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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

15 authors at 1 institution in 1 country.

Quirin NotzDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Würzburg, Würzburg, Germany.
Marc SchmalzingDepartment of Medicine II, Rheumatology and Clinical Immunology, University Hospital Würzburg, Würzburg, Germany.
Florian WedekinkDepartment of Gynecology, Section for Experimental Tumor Immunology, University Hospital Würzburg, Würzburg, Germany.
Tobias SchlesingerDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Würzburg, Würzburg, Germany.
Michael GernertDepartment of Medicine II, Rheumatology and Clinical Immunology, University Hospital Würzburg, Würzburg, Germany.
Johannes HerrmannDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Würzburg, Würzburg, Germany.
Lena SorgerDepartment of Gynecology, Section for Experimental Tumor Immunology, University Hospital Würzburg, Würzburg, Germany.
Dirk WeismannDepartment of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.
Benedikt SchmidDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Würzburg, Würzburg, Germany.
Magdalena SitterDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Würzburg, Würzburg, Germany.
Nicolas SchlegelDepartment of General, Visceral, Vascular and Pediatric Surgery (Surgery I), University Hospital Würzburg, Würzburg, Germany.
Peter KrankeDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Würzburg, Würzburg, Germany.
Jörg WischhusenDepartment of Gynecology, Section for Experimental Tumor Immunology, University Hospital Würzburg, Würzburg, Germany.
Patrick MeybohmDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Würzburg, Würzburg, Germany.
Christopher LotzDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Würzburg, Würzburg, Germany.
Universitätsklinikum Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: The severity of Coronavirus Disease 2019 (COVID-19) is largely determined by the immune response. First studies indicate altered lymphocyte counts and function. However, interactions of pro- and anti-inflammatory mechanisms remain elusive. In the current study we characterized the immune responses in patients suffering from severe COVID-19-induced acute respiratory distress syndrome (ARDS). Methods: This was a single-center retrospective study in patients admitted to the intensive care unit (ICU) with confirmed COVID-19 between March 14 Results: All patients suffered from severe ARDS, 30.8% died. Interleukin (IL)-6 was massively elevated at every time-point. The anti-inflammatory cytokine IL-10 was concomitantly upregulated with IL-6. The cellular response was characterized by lymphocytopenia with low counts of CD8+ T cells, natural killer (NK) and naïve T helper cells. CD8+ T and NK cells recovered after 8 to 14 days. The B cell system was largely unimpeded. This coincided with a slight increase in anti-SARS-CoV-2-Spike-RBD immunoglobulin (Ig) G and a decrease in anti-SARS-CoV-2-Spike-RBD IgM. GDF-15 levels were elevated throughout ICU treatment. Conclusions: Massively elevated levels of IL-6 and a delayed cytotoxic immune defense characterized severe COVID-19-induced ARDS. The B cell response and antibody production were largely unimpeded. No obvious imbalance of pro- and anti-inflammatory mechanisms was observed, with elevated GDF-15 levels suggesting increased tissue resilience.

Indexed as

AgedAntibodies, ViralBetacoronavirusCoronavirus InfectionsCOVID-19Cytokine Release SyndromeFemaleGrowth Differentiation Factor 15HumansImmunoglobulin GIntensive Care UnitsInterleukin-10Interleukin-6Longitudinal StudiesLymphopeniaMaleAntibodies, ViralGDF15 protein, humanGrowth Differentiation Factor 15IL10 protein, humanIL6 protein, humanImmunoglobulin GInterleukin-10Interleukin-6Spike Glycoprotein, Coronavirusspike protein, SARS-CoV-2acute respiratory distress syndromeCoronavirus Disease 2019cytokinesgrowth differentiation factor 15immune responseinflammationSevere Acute Respiratory Syndrome Coronavirus 2

Identifiers

PMID33123167
PMCPMC7573122
OpenAlexW3091927903

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.