Evidence map›Paper›PMID 35197972›Full record

ArticleFrontiers in immunology2022

Sustained Antibody-Dependent NK Cell Functions in Mild COVID-19 Outpatients During Convalescence.

Francisco Fuentes-Villalobos, Jose L Garrido, Matías A Medina, Nicole Zambrano, Natalia Ross, Felipe Bravo, Aracelly Gaete-Argel, Aarón Oyarzún-Arrau, Fatima Amanat, Ricardo Soto-Rifo and 15 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Tuberculosis treatment and cytotoxic immune signatures: a longitudinal study.Journal of clinical tuberculosis and other mycobacterial diseases · 2026
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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

25 authors at 9 institutions in 2 countries.

Francisco Fuentes-VillalobosDepartment of Microbiology, Faculty of Biological Science, Universidad de Concepción, Concepción, Chile.
Jose L GarridoIchor Biologics LLC, New York, NY, United States.
Matías A MedinaDepartment of Microbiology, Faculty of Biological Science, Universidad de Concepción, Concepción, Chile.
Nicole ZambranoDepartment of Microbiology, Faculty of Biological Science, Universidad de Concepción, Concepción, Chile.
Natalia RossDepartment of Microbiology, Faculty of Biological Science, Universidad de Concepción, Concepción, Chile.
Felipe BravoDepartment of Microbiology, Faculty of Biological Science, Universidad de Concepción, Concepción, Chile.
Aracelly Gaete-ArgelLaboratory of Molecular and Cellular Virology, Virology Program, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Aarón Oyarzún-ArrauLaboratory of Molecular and Cellular Virology, Virology Program, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Fatima AmanatDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Ricardo Soto-RifoLaboratory of Molecular and Cellular Virology, Virology Program, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Fernando Valiente-EcheverríaLaboratory of Molecular and Cellular Virology, Virology Program, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Renato OcampoHospital Regional de Talca, Talca, Chile.
Christian EsveileHospital Clínico Herminda Martin, Chillán, Chile.
Leonila FerreiraHospital Clínico Regional Dr. Guillermo Grant Benavente, Concepción, Chile.
Johanna CabreraHospital Dr. Hernán Henríquez Aravena, Temuco, Chile.
Vivianne TorresInstitute of Medicine, Faculty of Medicine, Universidad Austral de Chile, Valdivia, Chile.
Maria L RiosecoFacultad de Medicina y Ciencia, Universidad San Sebastián, Puerto Montt, Chile.
Raúl RiquelmeFacultad de Medicina y Ciencia, Universidad San Sebastián, Puerto Montt, Chile.
Sebastián BarríaHospital Puerto Montt Dr. Eduardo Schütz Schroeder, Puerto Montt, Chile.
Raymond AlvarezIchor Biologics LLC, New York, NY, United States.
Yazmín PinosHospital Base San José, Osorno, Chile.
Florian KrammerDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Mario CalvoInstitute of Medicine, Faculty of Medicine, Universidad Austral de Chile, Valdivia, Chile.
Maria I BarriaDepartment of Microbiology, Faculty of Biological Science, Universidad de Concepción, Concepción, Chile.
COVID-19 South Chile Group
University of Concepción · CLUniversity of Chile · CLIcahn School of Medicine at Mount Sinai · USSan Sebastián University · CLAustral University of Chile · CLHospital Base · CLHospital Doctor Hernán Henríquez Aravena · CLHospital Regional de Concepción · CLHospital Regional de Talca · CL

Funding

COLLABORATIVE INFLUENZA VACCINE INNOVATION CENTER: UNIVERSAL INFLUENZA VACCINE RESEARCH75N93019C00051 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KRAMMER, FLORIAN · 2019 to 2025
$105.4M
Development of broadly neutralizing antibodies to treat hantavirus infectionsR43AI138740 · NIAID · ICHOR BIOLOGICS, LLC · PI ALVAREZ, RAYMOND · 2019 to 2020
$355k
NIAID NIH HHS 75N93019C00051NIAID NIH HHS HHSN272201400008CNIAID NIH HHS R43 AI138740
6 · The paper itself

Abstract

The coronavirus disease 2019 (COVID19) pandemic has left researchers scrambling to identify the humoral immune correlates of protection from COVID-19. To date, the antibody mediated correlates of virus neutralization have been extensively studied. However, the extent that non-neutralizing functions contribute to anti-viral responses are ill defined. In this study, we profiled the anti-spike antibody subtype/subclass responses, along with neutralization and antibody-dependent natural killer cell functions in 83 blood samples collected between 4 and 201 days post-symptoms onset from a cohort of COVID-19 outpatients. We observed heterogeneous humoral responses against the acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein. Overall, anti-spike profiles were characterized by a rapid rise of IgA and sustained IgG titers. In addition, strong antibody-mediated natural killer effector responses correlated with milder disease and being female. While higher neutralization profiles were observed in males along with increased severity. These results give an insight into the underlying function of antibodies beyond neutralization and suggest that antibody-mediated natural killer cell activity is a key function of the humoral response against the SARS-CoV-2 spike protein.

Indexed as

ConvalescenceOutpatientsAdultAntibodies, NeutralizingAntibodies, ViralCOVID-19FemaleHEK293 CellsHumansKiller Cells, NaturalMaleMiddle AgedSARS-CoV-2Antibodies, NeutralizingAntibodies, ViralCOVID-19Fc-effector functionsNK cells activityoutpatientsSARS-CoV-2spike (S) glycoprotein

Identifiers

PMID35197972
PMCPMC8859986
OpenAlexW4210829967

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.