Evidence map›Paper›PMID 34805226›Full record

ArticleFrontiers in medicine2021

Impaired Dendritic Cell Homing in COVID-19.

Lukas Borcherding, Alime Sema Teksen, Bianca Grosser, Tina Schaller, Klaus Hirschbühl, Rainer Claus, Oliver Spring, Michael Wittmann, Christoph Römmele, Éva Sipos and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  7. Immune Cells in Subretinal Wound Healing and Fibrosis.Frontiers in cellular neuroscience · 2022
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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

11 authors at 2 institutions in 1 country.

Lukas BorcherdingGeneral Pathology and Molecular Diagnostics, Medical Faculty, University of Augsburg, Augsburg, Germany.
Alime Sema TeksenVisiopharm, Hørsholm, Denmark.
Bianca GrosserGeneral Pathology and Molecular Diagnostics, Medical Faculty, University of Augsburg, Augsburg, Germany.
Tina SchallerGeneral Pathology and Molecular Diagnostics, Medical Faculty, University of Augsburg, Augsburg, Germany.
Klaus HirschbühlHematology and Oncology, Medical Faculty, University of Augsburg, Augsburg, Germany.
Rainer ClausHematology and Oncology, Medical Faculty, University of Augsburg, Augsburg, Germany.
Oliver SpringAnesthesiology and Operative Intensive Care Medicine, Medical Faculty, University of Augsburg, Augsburg, Germany.
Michael WittmannHematology and Oncology, Medical Faculty, University of Augsburg, Augsburg, Germany.
Christoph RömmeleInternal Medicine III-Gastroenterology, University Hospital of Augsburg, Augsburg, Germany.
Éva SiposGeneral Pathology and Molecular Diagnostics, Medical Faculty, University of Augsburg, Augsburg, Germany.
Bruno MärklGeneral Pathology and Molecular Diagnostics, Medical Faculty, University of Augsburg, Augsburg, Germany.
University of Augsburg · DEUniversity Hospital Augsburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The high mortality of COVID-19 is mostly attributed to acute respiratory distress syndrome (ARDS), whose histopathological correlate is diffuse alveolar damage (DAD). Furthermore, severe COVID-19 is often accompanied by a cytokine storm and a disrupted response of the adaptive immune system. Studies aiming to depict this dysregulation have mostly investigated the peripheral cell count as well as the functionality of immune cells. We investigated the impact of SARS-CoV-2 on antigen-presenting cells using multiplexed immunofluorescence. Similar to MERS-CoV and SARS-CoV, SARS-CoV-2 appears to be impairing the maturation of dendritic cells (DCs). DC maturation involves a switch in surface antigen expression, which enables the cells' homing to lymph nodes and the subsequent activation of T-cells. As quantitative descriptions of the local inflammatory infiltrate are still scarce, we compared the cell population of professional antigen-presenting cells (APC) in the lungs of COVID-19 autopsy cases in different stages of DAD. We found an increased count of myeloid dendritic cells (mDCs) in later stages. Interestingly, mDCs also showed no significant upregulation of maturation markers in DAD-specimens with high viral load. Accumulation of immature mDCs, which are unable to home to lymph nodes, ultimately results in an inadequate T-cell response.

Indexed as

artificial intelligenceCOVID-19dendritic cellsdiffuse alveolar damage (DAD)homingmaturationmultiplexed immunofluorescenceSARS-CoV-2

Identifiers

PMID34805226
PMCPMC8601231
OpenAlexW3209297202

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.