Evidence map›Paper›PMID 41996420›Full record

ArticlePloS one2026

Distinct plasma cytokine and chemokine profiles in severe COVID-19 and septic shock.

Se Ju Lee, Jaehoon Kim, Min Han, Jung Ah Lee, Yongseop Lee, Jung Ho Kim, Jin Young Ahn, Su Jin Jeong, Nam Su Ku, Joon-Sup Yeom and 1 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Se Ju LeeDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jaehoon KimDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Min HanDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jung Ah LeeDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Yongseop LeeDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jung Ho KimDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jin Young AhnDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Su Jin JeongDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Nam Su KuDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Joon-Sup YeomDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-8940-7170
Jun Yong ChoiDivision of Infectious Diseases, Department of Internal Medicine and AIDS Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-2775-3315

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere Coronavirus Disease 2019 (COVID-19) and septic shock are both characterized by dysregulated host immune responses. While similarities and differences in immune responses between COVID-19 and bacterial sepsis have been reported, direct comparative analyses remain limited. This study aims to characterize the immunologic status of patients with COVID-19 and sepsis through plasma cytokine/chemokine analysis, thereby providing additional candidates for immunomodulatory therapy for COVID-19.

methodsWe included patients diagnosed with severe COVID-19 or septic shock with lymphopenia, matched for age, sex, steroid administration, and severity. A total of 20 analytes were measured using Luminex assay.

resultsA total of 36 patients were enrolled. Plasma granulocyte-macrophage colony-stimulating factor (GM-CSF) concentrations were significantly higher in the COVID-19 group (5.3 pg/ml; IQR, 3.6-16.3 vs 0.0 pg/ml; IQR, 0.0-3.6; P = 0.010). Plasma interleukin-10 (IL-10) (0.0 pg/ml; IQR, 0.0-4.8 vs 28.8 pg/ml; IQR, 7.5-51.7; P = 0.003) and IL-15 (0.0 pg/ml; IQR, 0.0-0.0 vs 0.0 pg/ml; IQR, 0.0-5.6; P = 0.024) levels were significantly higher in the sepsis group. Firth logistic regression analysis showed that plasma IL-6, IL-8, and CXCL16 levels were associated with new organ support in the sepsis group, while IL-15, CXCL16, and IL-1RA levels tended to be associated in the COVID-19 group.

conclusionAt day 7 after diagnosis, both groups exhibited active proinflammatory responses, but only the sepsis group showed prominent anti-inflammatory responses. The persistent elevation of GM-CSF in the COVID-19 group, even with steroid administration, highlights its potential as a therapeutic target and underscores the need for patient stratification in immunomodulatory trials.

Indexed as

ChemokinesCOVID-19CytokinesShock, SepticAgedFemaleGranulocyte-Macrophage Colony-Stimulating FactorHumansMaleMiddle AgedSARS-CoV-2Severity of Illness IndexChemokinesCytokinesGranulocyte-Macrophage Colony-Stimulating Factor

Identifiers

PMID41996420
PMCPMC13089746

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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.