Evidence map›Paper›PMID 34339730›Full record

ArticleThe Journal of allergy and clinical immunology2021

Abnormality in the NK-cell population is prolonged in severe COVID-19 patients.

Galam Leem, Shinhye Cheon, Hoyoung Lee, Seong Jin Choi, Seongju Jeong, Eui-Soon Kim, Hye Won Jeong, Hyeongseok Jeong, Su-Hyung Park, Yeon-Sook Kim and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 85 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

11 authors at 4 institutions in 1 country.

Galam LeemDivision of Gastroenterology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Shinhye CheonDivision of Infectious Diseases, Department of Internal Medicine, Chungnam National University School of Medicine, Daejeon, Korea.
Hoyoung LeeGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Seong Jin ChoiGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Seongju JeongGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Eui-Soon KimGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Hye Won JeongDepartment of Internal Medicine, Chungbuk National University College of Medicine, Cheongju, Korea.
Hyeongseok JeongDivision of Infectious Diseases, Department of Internal Medicine, Chungnam National University School of Medicine, Daejeon, Korea.
Su-Hyung ParkGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Yeon-Sook KimDivision of Infectious Diseases, Department of Internal Medicine, Chungnam National University School of Medicine, Daejeon, Korea. Electronic address: alice@cnuh.co.kr.
Eui-Cheol ShinGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea. Electronic address: ecshin@kaist.ac.kr.
Korea Advanced Institute of Science and Technology · KRChungbuk National University · KRChungnam National University · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOur understanding of adaptive immune responses in patients with coronavirus disease 2019 (COVID-19) is rapidly evolving, but information on the innate immune responses by natural killer (NK) cells is still insufficient.

objectiveWe aimed to examine the phenotypic and functional status of NK cells and their changes during the course of mild and severe COVID-19.

methodsWe performed RNA sequencing and flow cytometric analysis of NK cells from patients with mild and severe COVID-19 at multiple time points in the course of the disease using cryopreserved PBMCs.

resultsIn RNA-sequencing analysis, the NK cells exhibited distinctive features compared with healthy donors, with significant enrichment of proinflammatory cytokine-mediated signaling pathways. Intriguingly, we found that the unconventional CD56

conclusionsThe current longitudinal study provides a deep understanding of the NK-cell biology in COVID-19.

Indexed as

Lymphocyte ActivationAdultCOVID-19HumansKiller Cells, NaturalLongitudinal StudiesMaleMiddle AgedProspective StudiesRNA-SeqSARS-CoV-2COVID-19cytotoxicityinnate immunityNK cellsSARS-CoV-2unconventional CD56(dim)CD16(neg) (uCD56(dim)) NK cell

Identifiers

PMID34339730
PMCPMC8324384
OpenAlexW3191255054

What OpenQuestion holds

Textmetadata
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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.