Evidence map›Paper›PMID 36142255›Full record

ArticleInternational journal of molecular sciences2022

Role of Innate and Adaptive Cytokines in the Survival of COVID-19 Patients.

Jorge Monserrat, Ana Gómez-Lahoz, Miguel A Ortega, José Sanz, Benjamin Muñoz, Juan Arévalo-Serrano, José Miguel Rodríguez, Jose Maria Gasalla, Óscar Gasulla, Alberto Arranz and 8 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Dynamic Cytokine and Coagulation Profiling in Patients With Severe COVID‑19 Evaluated for Pulmonary Embolism: A Prospective Cohort Study.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Observational
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  12. Alterations in CX3CL1 Levels and Its Role in Viral Pathogenesis.International journal of molecular sciences · 2024
    Review
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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

18 authors at 6 institutions in 1 country.

Jorge MonserratDepartment of Medicine and Medical Specialities, Faculty of Medicine and Health Sciences, University of Alcalá, 28801 Alcalá de Henares, Spain.ORCID 0000-0003-1775-4645
Ana Gómez-LahozDepartment of Medicine and Medical Specialities, Faculty of Medicine and Health Sciences, University of Alcalá, 28801 Alcalá de Henares, Spain.
Miguel A OrtegaDepartment of Medicine and Medical Specialities, Faculty of Medicine and Health Sciences, University of Alcalá, 28801 Alcalá de Henares, Spain.ORCID 0000-0003-2588-1708
José SanzService of Internal Medicine and Immune System Diseases-Rheumatology, University Hospital Príncipe de Asturias (CIBEREHD), 28806 Alcalá de Henares, Spain.ORCID 0000-0003-3180-184X
Benjamin MuñozService of Internal Medicine and Immune System Diseases-Rheumatology, University Hospital Príncipe de Asturias (CIBEREHD), 28806 Alcalá de Henares, Spain.
Juan Arévalo-SerranoService of Internal Medicine and Immune System Diseases-Rheumatology, University Hospital Príncipe de Asturias (CIBEREHD), 28806 Alcalá de Henares, Spain.ORCID 0000-0003-2563-7860
José Miguel RodríguezService of Internal Medicine and Immune System Diseases-Rheumatology, University Hospital Príncipe de Asturias (CIBEREHD), 28806 Alcalá de Henares, Spain.ORCID 0000-0002-8446-3373
Jose Maria GasallaService of Internal Medicine and Immune System Diseases-Rheumatology, University Hospital Príncipe de Asturias (CIBEREHD), 28806 Alcalá de Henares, Spain.
Óscar GasullaHospital Universitari de Bellvitge, Universitat de Barcelona, 08907 L'Hospitalet de Llobregat, Spain.
Alberto ArranzDepartment of Surgery, Medical and Social Sciences, Faculty of Medicine and Health Sciences, University of Alcalá, 28801 Alcalá de Henares, Spain.
Jordi Fortuny-ProfitósCampus Nord, Universitat Politècnica de Catalunya, 08034 Barcelona, Spain.ORCID 0000-0002-4181-1593
Ferran A Mazaira-FontDepartament d'Econometria, Estadística I Economia Aplicada, Universitat de Barcelona, 08007 Barcelona, Spain.
Miguel Teixidó RománCampus Nord, Universitat Politècnica de Catalunya, 08034 Barcelona, Spain.
Carlos Martínez-ADepartment of Immunology and Oncology, Centro Nacional de Biotecnología/CSIC, 28006 Madrid, Spain.ORCID 0000-0002-2121-189X
Dimitri BalomenosDepartment of Immunology and Oncology, Centro Nacional de Biotecnología/CSIC, 28006 Madrid, Spain.
Angel AsunsoloRamón y Cajal Institute of Sanitary Research (IRYCIS), 28034 Madrid, Spain.ORCID 0000-0001-7898-4685
Melchor Álvarez-MonDepartment of Medicine and Medical Specialities, Faculty of Medicine and Health Sciences, University of Alcalá, 28801 Alcalá de Henares, Spain.ORCID 0000-0003-1309-7510
On Behalf Of The Covid-Hupa Group
Universidad de Alcalá · ESHospital Universitario Príncipe de Asturias · ESCentro Nacional de Biotecnología · ESUniversitat Politècnica de Catalunya · ESInstituto Cajal · ESUniversitat de Barcelona · ES

Funding

Comunidad de Madrid MITIC-CM
6 · The paper itself

Abstract

SARS-CoV-2 is a new coronavirus characterized by a high infection and transmission capacity. A significant number of patients develop inadequate immune responses that produce massive releases of cytokines that compromise their survival. Soluble factors are clinically and pathologically relevant in COVID-19 survival but remain only partially characterized. The objective of this work was to simultaneously study 62 circulating soluble factors, including innate and adaptive cytokines and their soluble receptors, chemokines and growth and wound-healing/repair factors, in severe COVID-19 patients who survived compared to those with fatal outcomes. Serum samples were obtained from 286 COVID-19 patients and 40 healthy controls. The 62 circulating soluble factors were quantified using a Luminex Milliplex assay. Results. The patients who survived had decreased levels of the following 30 soluble factors of the 62 studied compared to those with fatal outcomes, therefore, these decreases were observed for cytokines and receptors predominantly produced by the innate immune system-IL-1α, IL-1α, IL-18, IL-15, IL-12p40, IL-6, IL-27, IL-1Ra, IL-1RI, IL-1RII, TNFα, TGFα, IL-10, sRAGE, sTNF-RI and sTNF-RII-for the chemokines IL-8, IP-10, MCP-1, MCP-3, MIG and fractalkine; for the growth factors M-CSF and the soluble receptor sIL2Ra; for the cytokines involved in the adaptive immune system IFNγ, IL-17 and sIL-4R; and for the wound-repair factor FGF2. On the other hand, the patients who survived had elevated levels of the soluble factors TNFβ, sCD40L, MDC, RANTES, G-CSF, GM-CSF, EGF, PDGFAA and PDGFABBB compared to those who died. Conclusions. Increases in the circulating levels of the sCD40L cytokine; MDC and RANTES chemokines; the G-CSF and GM-CSF growth factors, EGF, PDGFAA and PDGFABBB; and tissue-repair factors are strongly associated with survival. By contrast, large increases in IL-15, IL-6, IL-18, IL-27 and IL-10; the sIL-1RI, sIL1RII and sTNF-RII receptors; the MCP3, IL-8, MIG and IP-10 chemokines; the M-CSF and sIL-2Ra growth factors; and the wound-healing factor FGF2 favor fatal outcomes of the disease.

Indexed as

COVID-19Interleukin-27Chemokine CCL5Chemokine CX3CL1Chemokine CXCL10CytokinesEpidermal Growth FactorFibroblast Growth Factor 2Granulocyte Colony-Stimulating FactorGranulocyte-Macrophage Colony-Stimulating FactorHumansInterleukin-10Interleukin-12 Subunit p40Interleukin-15Interleukin-17Interleukin-18Chemokine CCL5Chemokine CX3CL1Chemokine CXCL10CytokinesEpidermal Growth FactorFibroblast Growth Factor 2Granulocyte Colony-Stimulating FactorGranulocyte-Macrophage Colony-Stimulating FactorInterleukin-10Interleukin-12 Subunit p40Interleukin-15Interleukin-17Interleukin-18Interleukin 1 Receptor Antagonist ProteinInterleukin-27Interleukin-6Interleukin-8Macrophage Colony-Stimulating FactorTransforming Growth Factor alphaTumor Necrosis Factor-alphabiomarkerschemokinesCOVID-19growth factorsinnate and adaptive cytokinesprognosis

Identifiers

PMID36142255
PMCPMC9499609
OpenAlexW4294934803

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.