Evidence map›Paper›PMID 37081872›Full record

ArticleFrontiers in immunology2023

Different degree of cytokinemia and T-cell activation according to serum IL-6 levels in critical COVID-19.

Chan Mi Lee, Minji Kim, Chang Kyung Kang, Pyoeng Gyun Choe, Nam Joong Kim, Hyeeun Bang, Taeeun Cho, Hyun Mu Shin, Hang-Rae Kim, Wan Beom Park and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 95% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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

11 authors at 1 institution in 1 country.

Chan Mi LeeDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Minji KimDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Republic of Korea.
Chang Kyung KangDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Pyoeng Gyun ChoeDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Nam Joong KimDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Hyeeun BangResearch and development team 2, Molecular Diagnostics Division, Quantamatrix Inc., Seoul, Republic of Korea.
Taeeun ChoResearch and development team 2, Molecular Diagnostics Division, Quantamatrix Inc., Seoul, Republic of Korea.
Hyun Mu ShinDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Republic of Korea.
Hang-Rae KimDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Republic of Korea.
Wan Beom ParkDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Myoung-Don OhDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Seoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Tocilizumab, a humanized anti-interleukin-6 receptor (IL-6R) antibody, is recommended for the treatment of severe to critical coronavirus diseases 2019 (COVID-19). However, there were conflicting results on the efficacy of tocilizumab. Therefore, we hypothesized that the differences in tocilizumab efficacy may stem from the different immune responses of critical COVID-19 patients. In this study, we described two groups of immunologically distinct COVID-19 patients, based on their IL-6 response. Methods: We prospectively enrolled critical COVID-19 patients, requiring oxygen support with a high flow nasal cannula or a mechanical ventilator, and analyzed their serial samples. An enzyme-linked immunosorbent assay and flow cytometry were used to evaluate the cytokine kinetics and cellular immune responses, respectively. Results: A total of nine patients with critical COVID-19 were included. The high ( Conclusion: There were distinctive two groups of critical COVID-19 according to serum IL-6 levels having different degrees of cytokinemia and T-cell responses. Our results indicate that the use of immune modulators should be more tailored in patients with critical COVID-19.

Indexed as

CD8-Positive T-LymphocytesCOVID-19CytokinesHLA-DR AntigensHumansInterleukin-6CytokinesHLA-DR AntigensInterleukin-6critical COVID-19cytokineIL-6immune responseT cell

Identifiers

PMID37081872
PMCPMC10110916
OpenAlexW4362639994

What OpenQuestion holds

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LicenceCC BY
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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.