Evidence map›Paper›PMID 34476598›Full record

ArticleIntensive care medicine experimental2021

Killer immunoglobulin-like receptor 2DS5 is associated with recovery from coronavirus disease 2019.

Vadim Lesan, Moritz Bewarder, Carlos Metz, André Becker, Sebastian Mang, Evi Regitz, Lorenz Thurner, Frank Neumann, Igor Kos, Konstantinos Christofyllakis and 6 more

Open access · goldAbstract read
In one paragraph

Article in Intensive care medicine experimental, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
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

16 authors at 1 institution in 1 country.

Vadim LesanDepartment of Internal Medicine I (Oncology, Hematology, Clinical Immunology, Rheumatology), Saarland University Medical Center, University Hospital, Saarland, 66421, Homburg, Germany. vadim.lesan@uks.eu.ORCID http://orcid.org/0000-0002-2600-2122
Moritz BewarderDepartment of Internal Medicine I (Oncology, Hematology, Clinical Immunology, Rheumatology), Saarland University Medical Center, University Hospital, Saarland, 66421, Homburg, Germany.
Carlos MetzDepartment of Internal Medicine V (Pneumology, Allergology and Critical Care Medicine), Interdisciplinary COVID-19 Center, University Hospital, Saarland, Homburg, Germany.
André BeckerDepartment of Internal Medicine V (Pneumology, Allergology and Critical Care Medicine), Interdisciplinary COVID-19 Center, University Hospital, Saarland, Homburg, Germany.
Sebastian MangDepartment of Internal Medicine V (Pneumology, Allergology and Critical Care Medicine), Interdisciplinary COVID-19 Center, University Hospital, Saarland, Homburg, Germany.
Evi RegitzDepartment of Internal Medicine I (Oncology, Hematology, Clinical Immunology, Rheumatology), Saarland University Medical Center, University Hospital, Saarland, 66421, Homburg, Germany.
Lorenz ThurnerDepartment of Internal Medicine I (Oncology, Hematology, Clinical Immunology, Rheumatology), Saarland University Medical Center, University Hospital, Saarland, 66421, Homburg, Germany.
Frank NeumannDepartment of Internal Medicine I (Oncology, Hematology, Clinical Immunology, Rheumatology), Saarland University Medical Center, University Hospital, Saarland, 66421, Homburg, Germany.
Igor KosDepartment of Internal Medicine I (Oncology, Hematology, Clinical Immunology, Rheumatology), Saarland University Medical Center, University Hospital, Saarland, 66421, Homburg, Germany.
Konstantinos ChristofyllakisDepartment of Internal Medicine I (Oncology, Hematology, Clinical Immunology, Rheumatology), Saarland University Medical Center, University Hospital, Saarland, 66421, Homburg, Germany.
Guy DanzigerDepartment of Internal Medicine V (Pneumology, Allergology and Critical Care Medicine), Interdisciplinary COVID-19 Center, University Hospital, Saarland, Homburg, Germany.
Stephan StilgenbauerDepartment of Internal Medicine I (Oncology, Hematology, Clinical Immunology, Rheumatology), Saarland University Medical Center, University Hospital, Saarland, 66421, Homburg, Germany.
Robert BalsDepartment of Internal Medicine V (Pneumology, Allergology and Critical Care Medicine), Interdisciplinary COVID-19 Center, University Hospital, Saarland, Homburg, Germany.
Philipp M LepperDepartment of Internal Medicine V (Pneumology, Allergology and Critical Care Medicine), Interdisciplinary COVID-19 Center, University Hospital, Saarland, Homburg, Germany.
Dominic Kaddu-Mulindwa *Department of Internal Medicine I (Oncology, Hematology, Clinical Immunology, Rheumatology), Saarland University Medical Center, University Hospital, Saarland, 66421, Homburg, Germany.
Torben Rixecker *Department of Internal Medicine V (Pneumology, Allergology and Critical Care Medicine), Interdisciplinary COVID-19 Center, University Hospital, Saarland, Homburg, Germany.
Saarland University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite numerous advances in the identification of risk factors for the development of severe coronavirus disease 2019 (COVID-19), factors that promote recovery from COVID-19 remain unknown. Natural killer (NK) cells provide innate immune defense against viral infections and are known to be activated during moderate and severe COVID-19. Killer immunoglobulin-like receptors (KIR) mediate NK cell cytotoxicity through recognition of an altered MHC-I expression on infected target cells. However, the influence of KIR genotype on outcome of patients with COVID-19 has not been investigated so far. We retrospectively analyzed the outcome associations of NK cell count and KIR genotype of patients with COVID-19 related severe ARDS treated on our tertiary intensive care unit (ICU) between February and June 2020 and validated our findings in an independent validation cohort of patients with moderate COVID-19 admitted to our tertiary medical center.

resultsMedian age of all patients in the discovery cohort (n = 16) was 61 years (range 50-71 years). All patients received invasive mechanical ventilation; 11 patients (68%) required extracorporeal membrane oxygenation (ECMO). Patients who recovered from COVID-19 had significantly higher median NK cell counts during the whole observational period compared to patients who died (121 cells/µL, range 16-602 cells/µL vs 81 cells/µL, range 6-227 cells/µL, p-value = 0.01). KIR2DS5 positivity was significantly associated with shorter time to recovery (21.6 ± 2.8 days vs. 44.6 ± 2.2 days, p-value = 0.01). KIR2DS5 positivity was significantly associated with freedom from transfer to ICU (0% vs 9%, p-value = 0.04) in the validation cohort which consisted of 65 patients with moderate COVID-19.

conclusionNK cells and KIR genotype might have an impact on recovery from COVID-19.

Indexed as

ARDSCOVID-19Intensive care unitKIRNK cellsSARS-CoV-2

Identifiers

PMID34476598
PMCPMC8412971
OpenAlexW3197259009

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.