Evidence map›Paper›PMID 33979758›Full record

Observational studyEBioMedicine2021

Blood neutrophils from children with COVID-19 exhibit both inflammatory and anti-inflammatory markers.

Vanesa Seery, Silvina C Raiden, Silvia C Algieri, Nicolás A Grisolía, Daniela Filippo, Norberto De Carli, Sandra Di Lalla, Héctor Cairoli, María J Chiolo, Claudia N Meregalli and 26 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in EBioMedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.9field-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

28 citing papers in PubMed, 50 citations in OpenAlex.

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  17. Multisystem Inflammatory Syndrome in Children: Host Immunologic Responses.Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2022
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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

36 authors at 4 institutions in 1 country.

Vanesa SeeryInstituto de Investigaciones Biomédicas en Retrovirus y SIDA, Facultad de Medicina. UBA-CONICET, Paraguay 2155, C1121ABG CABA, Argentina.
Silvina C RaidenDepartamento de Medicina, Hospital General de Niños Pedro de Elizalde. Av. Montes de Oca 40, CABA C1270, Argentina.
Silvia C AlgieriServicio de Pediatría, Hospital Nacional Profesor Alejandro Posadas, Marconi Morón 386, Buenos Aires B1684, Argentina.
Nicolás A GrisolíaDepartamento de Medicina, Hospital General de Niños Pedro de Elizalde. Av. Montes de Oca 40, CABA C1270, Argentina.
Daniela FilippoServicio de Pediatría, Hospital Municipal Diego Thompson. Avellaneda 33, Buenos Aires B1650, Argentina.
Norberto De CarliServicio de Pediatría, Clínica del Niño de Quilmes, Av. Lamadrid 444, Buenos Aires B1878, Argentina.
Sandra Di LallaDepartamento de Consultorios Externos, Hospital General de Niños Pedro de Elizalde, Av. Montes de Oca 40, CABA C1270, Argentina.
Héctor CairoliDepartamento de Medicina, Hospital General de Niños Pedro de Elizalde. Av. Montes de Oca 40, CABA C1270, Argentina.
María J ChioloDepartamento de Cirugía, Hospital General de Niños Pedro de Elizalde, Av. Montes de Oca 40, CABA C1270, Argentina.
Claudia N MeregalliUnidad de Terapia Intensiva Pediátrica, Departamento de Urgencias, Hospital General de Niños Pedro de Elizalde. Av. Montes de Oca 40, CABA C1270, Argentina.
Lorena I GimenezServicio de Pediatría, Hospital Municipal Diego Thompson. Avellaneda 33, Buenos Aires B1650, Argentina.
Gabriela GregorioServicio de Pediatría, Hospital Nacional Profesor Alejandro Posadas, Marconi Morón 386, Buenos Aires B1684, Argentina.
Mariam SarliUnidad de Terapia Intensiva Pediátrica, Hospital Nacional Profesor Alejandro Posadas, Marconi Morón 386, Buenos Aires B1684, Argentina.
Ana L AlcaldeServicio de Pediatría, Hospital Nacional Profesor Alejandro Posadas, Marconi Morón 386, Buenos Aires B1684, Argentina.
Carolina DavenportDepartamento de Medicina, Hospital General de Niños Pedro de Elizalde. Av. Montes de Oca 40, CABA C1270, Argentina.
María J BrueraUnidad de Terapia Intensiva Pediátrica, Hospital Nacional Profesor Alejandro Posadas, Marconi Morón 386, Buenos Aires B1684, Argentina.
Nancy SimazServicio de Pediatría, Hospital Nacional Profesor Alejandro Posadas, Marconi Morón 386, Buenos Aires B1684, Argentina.
Mariela F PérezServicio de Pediatría, Hospital Nacional Profesor Alejandro Posadas, Marconi Morón 386, Buenos Aires B1684, Argentina.
Valeria NivelaDepartamento de Emergencias Pediátrica, Hospital Nacional Profesor Alejandro Posadas, Marconi Morón 386, Buenos Aires B1684, Argentina.
Carola BayleDepartamento de Emergencias Pediátrica, Hospital Nacional Profesor Alejandro Posadas, Marconi Morón 386, Buenos Aires B1684, Argentina.
Patricia TuccilloServicio de Pediatría, Hospital Naval Cirujano Mayor Dr. Pedro Mallo, Av. Patricias Argentinas 351, CABA C1405, Argentina.
María T AgostaServicio de Pediatría, Hospital Naval Cirujano Mayor Dr. Pedro Mallo, Av. Patricias Argentinas 351, CABA C1405, Argentina.
Hernán PérezServicio de Pediatría, Hospital Naval Cirujano Mayor Dr. Pedro Mallo, Av. Patricias Argentinas 351, CABA C1405, Argentina.
Susana Villa NovaServicio de Pediatría, Hospital General de Agudos Dr. Juan A. Fernández, Av. Cerviño 3356, CABA C1425, Argentina.
Patricia SuárezServicio de Pediatría, Hospital General de Agudos Dr. Juan A. Fernández, Av. Cerviño 3356, CABA C1425, Argentina.
Eugenia M TakataServicio de Pediatría, Hospital General de Agudos Dr. Juan A. Fernández, Av. Cerviño 3356, CABA C1425, Argentina.
Mariela GarcíaServicio de Pediatría, Hospital General de Agudos Dr. Juan A. Fernández, Av. Cerviño 3356, CABA C1425, Argentina.
Jorge LattnerServicio de Infectología Pediátrica, Hospital Naval Cirujano Mayor Dr. Pedro Mallo, Av. Patricias Argentinas 351, CABA C1405, Argentina.
María J RolónDivisión Infectología, Hospital General de Agudos Dr. Juan A. Fernández, Av. Cerviño 3356, CABA C1425, Argentina.
Patricia CollDivisión Infectología, Hospital General de Agudos Dr. Juan A. Fernández, Av. Cerviño 3356, CABA C1425, Argentina.
Inés SananezInstituto de Investigaciones Biomédicas en Retrovirus y SIDA, Facultad de Medicina. UBA-CONICET, Paraguay 2155, C1121ABG CABA, Argentina.
María P HolgadoInstituto de Investigaciones Biomédicas en Retrovirus y SIDA, Facultad de Medicina. UBA-CONICET, Paraguay 2155, C1121ABG CABA, Argentina.
Fernando FerreroDepartamento de Medicina, Hospital General de Niños Pedro de Elizalde. Av. Montes de Oca 40, CABA C1270, Argentina.
Jorge GeffnerInstituto de Investigaciones Biomédicas en Retrovirus y SIDA, Facultad de Medicina. UBA-CONICET, Paraguay 2155, C1121ABG CABA, Argentina.
Lourdes ArruvitoInstituto de Investigaciones Biomédicas en Retrovirus y SIDA, Facultad de Medicina. UBA-CONICET, Paraguay 2155, C1121ABG CABA, Argentina. Electronic address: arruvitol@gmail.com.
1 in behalf of the COVID-19 Naval Pediatric Workgroup and in behalf of the COVID-19, Fernández Pediatric Residency Workgroup
Hospital Posadas · ARHospital Pedro de Elizalde · ARHospital Fernández · ARConsejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPerhaps reflecting that children with COVID-19 rarely exhibit severe respiratory symptoms and often remain asymptomatic, little attention has been paid to explore the immune response in pediatric COVID-19. Here, we analyzed the phenotype and function of circulating neutrophils from children with COVID-19.

methodsAn observational study including 182 children with COVID-19, 21 children with multisystem inflammatory syndrome (MIS-C), and 40 healthy children was performed in Buenos Aires, Argentina. Neutrophil phenotype was analyzed by flow cytometry in blood samples. Cytokine production, plasma levels of IgG antibodies directed to the spike protein of SARS-CoV-2 and citrullinated histone H3 were measured by ELISA. Cell-free DNA was quantified by fluorometry.

findingsCompared with healthy controls, neutrophils from children with COVID-19 showed a lower expression of CD11b, CD66b, and L-selectin but a higher expression of the activation markers HLA-DR, CD64 and PECAM-1 and the inhibitory receptors LAIR-1 and PD-L1. No differences in the production of cytokines and NETs were observed. Interestingly, the expression of CD64 in neutrophils and the serum concentration of IgG antibodies directed to the spike protein of SARS-CoV-2 distinguished asymptomatic from mild and moderate COVID-19.

interpretationAcute lung injury is a prominent feature of severe COVID-19 in adults. A low expression of adhesion molecules together with a high expression of inhibitory receptors in neutrophils from children with COVID-19 might prevent tissue infiltration by neutrophils preserving lung function.

fundingThis study was supported by the Ministry of Science and Technology (National Agency for Scientific and Technological Promotion, IP-COVID-19-0277 and PMO BID PICT 2018-2548), and University of Buenos Aires from Argentina (20020170100573BA).

Indexed as

Antibodies, ViralArgentinaBiomarkersCase-Control StudiesChildChild, PreschoolCOVID-19CytokinesFemaleFlow CytometryHumansImmunoglobulin GInfantMaleNeutrophilsSARS-CoV-2Antibodies, ViralBiomarkersCytokinesImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Cell-adhesion moleculesFcγ receptorIgGInhibitory ReceptorsNeutrophilsPediatric COVID-19

Identifiers

PMID33979758
PMCPMC8153212
OpenAlexW3145863135

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.