Evidence map›Paper›PMID 39408857›Full record

ArticleInternational journal of molecular sciences2024

IFN Lambda Deficiency Contributes to Severe COVID-19 Outcomes.

Anna Zaleska, Anna Dor-Wojnarowska, Anna Radlińska, Marta Rorat, Wojciech Szymański, Adrian Gajewski, Maciej Chałubiński

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Anna ZaleskaDepartment of Allergology and Internal Medicine, Wroclaw Medical University, 50-368 Wroclaw, Poland.ORCID 0000-0002-7513-8042
Anna Dor-WojnarowskaDepartment of Allergology and Internal Medicine, Wroclaw Medical University, 50-368 Wroclaw, Poland.ORCID 0000-0002-1437-1668
Anna RadlińskaDepartment of Allergology and Internal Medicine, Wroclaw Medical University, 50-368 Wroclaw, Poland.
Marta RoratDepartment of Social Sciences and Infectious Diseases, Wroclaw University of Science and Technology, 50-370 Wroclaw, Poland.ORCID 0000-0002-5318-4945
Wojciech SzymańskiDepartment of Infectious Diseases and Hepatology, Wroclaw Medical University, 50-367 Wroclaw, Poland.ORCID 0000-0001-6605-6718
Adrian GajewskiDepartment of Immunology and Allergy, Medical University of Lodz, 92-213 Lodz, Poland.ORCID 0000-0001-7445-9752
Maciej ChałubińskiDepartment of Immunology and Allergy, Medical University of Lodz, 92-213 Lodz, Poland.ORCID 0000-0001-8311-9530

Funding

Ministry of Health subvention STM.A200.21.060
6 · The paper itself

Abstract

Interferons (IFNs) produced by airway epithelial cells are crucial in defending against pathogens. Fluctuations in IFN-λ levels may influence coronavirus disease 19 (COVID-19) severity. However, conflicting data have been reported regarding serum IFN-λ concentrations in COVID-19 patients. To address this, we evaluated serum IFN-λ levels over time in moderate and severe COVID-19 patients and their association with cytokine production and clinical parameters using the enzyme-linked immunosorbent assay (ELISA) and the Bio-Plex Pro Human Cytokine 17-plex Assay. Results from testing 51 COVID-19 patients showed that 68% lacked detectable serum IFN-λ. Among non-IFN-λ secretors, severe COVID-19 predominated. In contrast, IFN-λ secretors displayed stable IFN-λ levels in moderate cases, while severe cases showed a decline over time, which persisted even after recovery. A negative correlation was observed between IFN-λ levels and inflammatory markers. This, combined with an increase in tumor necrosis factor alpha (TNF-α) and clinical improvement, suggests a regulatory role for IFN-λ in promoting faster recovery. Despite this, survival rates were similar between the groups, indicating that while IFN-λ influences the course of the disease, it does not directly affect overall survival. In conclusion, IFN-λ is vital, but not unique, for the antiviral response and COVID-19 recovery. Simultaneously, serum IFN-λ deficiency signifies severe COVID-19.

Indexed as

COVID-19SARS-CoV-2AdultAgedCytokinesFemaleHumansInterferon LambdaInterferonsInterleukinsMaleMiddle AgedSeverity of Illness IndexTumor Necrosis Factor-alphaCytokinesInterferon Lambdainterferon-lambda, humanInterferonsInterleukinsTumor Necrosis Factor-alphaCOVID-19innate immunityinterferonSARS-CoV-2

Identifiers

PMID39408857
PMCPMC11476353

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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.