Evidence map›Paper›PMID 34122423›Full record

ArticleFrontiers in immunology

Impaired Cytotoxic Response in PBMCs From Patients With COVID-19 Admitted to the ICU: Biomarkers to Predict Disease Severity.

Lorena Vigón, Daniel Fuertes, Javier García-Pérez, Montserrat Torres, Sara Rodríguez-Mora, Elena Mateos, Magdalena Corona, Adolfo J Saez-Marín, Rosa Malo, Cristina Navarro and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.1field-weighted citation impact, top 10% 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

34 citing papers in PubMed, 40 citations in OpenAlex.

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  13. Alterations in the CD56International journal of molecular sciences · 2023
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  17. Multifaceted roles of Fcγ receptors in COVID-19 and vaccine responses.American journal of translational research · 2023
    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

17 authors at 8 institutions in 2 countries.

Lorena VigónImmunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Daniel FuertesSchool of Telecommunications Engineering, Universidad Politécnica de Madrid, Madrid, Spain.
Javier García-PérezImmunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Montserrat TorresImmunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Sara Rodríguez-MoraImmunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Elena MateosImmunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Magdalena CoronaHematology Service, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Adolfo J Saez-MarínHematology Service, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Rosa MaloNeumology Service, Hospital Universitario Puerta de Hierro, Majadahonda, Spain.
Cristina NavarroNeumology Service, Hospital de El Escorial, El Escorial, Spain.
María Aranzazu Murciano-AntónFamily Medicine, Centro de Salud Doctor Pedro Laín Entralgo, Alcorcón, Spain.
Miguel CerveroInternal Medicine Service, Hospital Universitario Severo Ochoa, Leganés, Spain.
José AlcamíImmunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Valentín García-GutiérrezHematology Service, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Vicente PlanellesDivision of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, UT, United States.
María Rosa López-HuertasImmunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Mayte CoirasImmunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, Madrid, Spain.
Instituto de Salud Carlos III · ESHospital Universitario Ramón y Cajal · ESCentro de Salud Casa del Barco · ESHospital El Escorial · ESHospital Universitario Puerta de Hierro Majadahonda · ESHospital Universitario Severo Ochoa · ESUniversidad Politécnica de Madrid · ESUniversity of Utah · US

Funding

Tyrosine Kinase inhibition: The New Front in HIV Cure EffortsR01AI143567 · NIAID · UNIVERSITY OF UTAH · PI COIRAS, MAYTE, PLANELLES, VICENTE · 2019 to 2023
$2.3M
NIAID NIH HHS R01 AI143567
6 · The paper itself

Abstract

Infection by novel coronavirus SARS-CoV-2 causes different presentations of COVID-19 and some patients may progress to a critical, fatal form of the disease that requires their admission to ICU and invasive mechanical ventilation. In order to predict in advance which patients could be more susceptible to develop a critical form of COVID-19, it is essential to define the most adequate biomarkers. In this study, we analyzed several parameters related to the cellular immune response in blood samples from 109 patients with different presentations of COVID-19 who were recruited in Hospitals and Primary Healthcare Centers in Madrid, Spain, during the first pandemic peak between April and June 2020. Hospitalized patients with the most severe forms of COVID-19 showed a potent inflammatory response that was not translated into an efficient immune response. Despite the high levels of effector cytotoxic cell populations such as NK, NKT and CD8+ T cells, they displayed immune exhaustion markers and poor cytotoxic functionality against target cells infected with pseudotyped SARS-CoV-2 or cells lacking MHC class I molecules. Moreover, patients with critical COVID-19 showed low levels of the highly cytotoxic TCRγδ+ CD8+ T cell subpopulation. Conversely, CD4 count was greatly reduced in association to high levels of Tregs, low plasma IL-2 and impaired Th1 differentiation. The relative importance of these immunological parameters to predict COVID-19 severity was analyzed by Random Forest algorithm and we concluded that the most important features were related to an efficient cytotoxic response. Therefore, efforts to fight against SARS-CoV-2 infection should be focused not only to decrease the disproportionate inflammatory response, but also to elicit an efficient cytotoxic response against the infected cells and to reduce viral replication.

Indexed as

Cytotoxicity, ImmunologicIntensive Care UnitsAdultAgedAged, 80 and overAntibodies, ViralBiomarkersComorbidityCOVID-19CytokinesFemaleHumansImmunophenotypingLeukocytes, MononuclearMaleMiddle AgedAntibodies, ViralBiomarkersCytokinesCD8 lymphocytes +COVID-19cytotoxic responseNK and NKT cellsSARS-CoV-2

Identifiers

PMID34122423
PMCPMC8187764
OpenAlexW3164880073

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.