Evidence map›Paper›PMID 34659245›Full record

ArticleFrontiers in immunology2021

Mild and Asymptomatic COVID-19 Convalescents Present Long-Term Endotype of Immunosuppression Associated With Neutrophil Subsets Possessing Regulatory Functions.

Izabela Siemińska, Kazimierz Węglarczyk, Marcin Surmiak, Dorota Kurowska-Baran, Marek Sanak, Maciej Siedlar, Jarek Baran

Abstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
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

30 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Neutrophils and NETs in kidney disease.Nature reviews. Nephrology · 2025
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Here, There, and Everywhere: Myeloid-Derived Suppressor Cells in Immunology.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  15. Review
  16. Suppressive myeloid cells in SARS-CoV-2 andFrontiers in immunology · 2023
    Article
  17. Article
  18. Article
  19. Review
  20. Myeloid-derived suppressor cells in COVID-19: A review.Clinical immunology (Orlando, Fla.) · 2022
    Review
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

7 authors.

Izabela SiemińskaDepartment of Clinical Immunology, Jagiellonian University Medical College, Krakow, Poland.
Kazimierz WęglarczykDepartment of Clinical Immunology, Jagiellonian University Medical College, Krakow, Poland.
Marcin SurmiakDepartment of Internal Medicine, Jagiellonian University Medical College, Krakow, Poland.
Dorota Kurowska-BaranDepartment of Clinical Microbiology, Laboratory of Virology and Serology, University Children's Hospital, Krakow, Poland.
Marek SanakDepartment of Internal Medicine, Jagiellonian University Medical College, Krakow, Poland.
Maciej SiedlarDepartment of Clinical Immunology, Jagiellonian University Medical College, Krakow, Poland.
Jarek BaranDepartment of Clinical Immunology, Jagiellonian University Medical College, Krakow, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SARS-CoV-2 infection [coronavirus disease 2019 (COVID-19)] is associated with severe lymphopenia and impaired immune response, including expansion of myeloid cells with regulatory functions, e.g., so-called low-density neutrophils, containing granulocytic myeloid-derived suppressor cells (LDNs/PMN-MDSCs). These cells have been described in both infections and cancer and are known for their immunosuppressive activity. In the case of COVID-19, long-term complications have been frequently observed (long-COVID). In this context, we aimed to investigate the immune response of COVID-19 convalescents after a mild or asymptomatic course of disease. We enrolled 13 convalescents who underwent a mild or asymptomatic infection with SARS-CoV-2, confirmed by a positive result of the PCR test, and 13 healthy donors without SARS-CoV-2 infection in the past. Whole blood was used for T-cell subpopulation and LDNs/PMN-MDSCs analysis. LDNs/PMN-MDSCs and normal density neutrophils (NDNs) were sorted out by FACS and used for T-cell proliferation assay with autologous T cells activated with anti-CD3 mAb. Serum samples were used for the detection of anti-SARS-CoV-2 neutralizing IgG and GM-CSF concentration. Our results showed that in convalescents, even 3 months after infection, an elevated level of LDNs/PMN-MDSCs is still maintained in the blood, which correlates negatively with the level of CD8

Indexed as

AdultAntibodies, NeutralizingAntibodies, ViralAsymptomatic InfectionsCD8-Positive T-LymphocytesCell ProliferationCOVID-19FemaleGranulocyte-Macrophage Colony-Stimulating FactorHumansImmunocompromised HostImmunoglobulin GLymphocyte ActivationMaleMiddle AgedMyeloid-Derived Suppressor CellsAntibodies, NeutralizingAntibodies, ViralGranulocyte-Macrophage Colony-Stimulating FactorImmunoglobulin GCOVID-19 convalescentsgranulocyte-macrophage colony stimulating factor (GM-CSF)granulocytic myeloid-derived suppressor cells (PMN-MDSCs)immunosuppressionlow-density neutrophils (LDNs)normal density neutrophils

Identifiers

PMID34659245
PMCPMC8511487

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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.