Evidence map›Paper›PMID 36219482›Full record

ArticleThe Journal of clinical investigation2022

Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody.

Tanushree Dangi, Sarah Sanchez, Jacob Class, Michelle Richner, Lavanya Visvabharathy, Young Rock Chung, Kirsten Bentley, Richard J Stanton, Igor J Koralnik, Justin M Richner and 1 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

54 citing papers in PubMed, 75 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Tanushree DangiDepartment of Microbiology and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Sarah SanchezDepartment of Microbiology and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Jacob ClassDepartment of Microbiology and Immunology, University of Illinois College of Medicine at Chicago, Chicago, Illinois, USA.
Michelle RichnerDepartment of Microbiology and Immunology, University of Illinois College of Medicine at Chicago, Chicago, Illinois, USA.
Lavanya VisvabharathyKen and Ruth Davee Department of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Young Rock ChungDepartment of Microbiology and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Kirsten BentleyDivision of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Richard J StantonDivision of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Igor J KoralnikKen and Ruth Davee Department of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Justin M RichnerDepartment of Microbiology and Immunology, University of Illinois College of Medicine at Chicago, Chicago, Illinois, USA.
Pablo Penaloza-MacMasterDepartment of Microbiology and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Northwestern University · USUniversity of Illinois Chicago · USCardiff University · GB

Funding

The Center for Innovation in Point-of-Care Technologies for HIV/AIDS atNorthwestern University (C-THAN) Supplemental RequestU54EB027049 · NIBIB · NORTHWESTERN UNIVERSITY · PI Chad J Achenbach · 2018 to 2026
$24.0M
Interferon-modulated vaccines against HIVDP2DA051912 · NIDA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PENALOZA, PABLO · 2020 to 2023
$2.7M
Dengue virus mRNA lipid nanoparticle vaccineR01AI150672 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RICHNER, JUSTIN · 2021 to 2024
$2.3M
Medical Research Council MR/S00971X/1NIAID NIH HHS R01 AI150672NIBIB NIH HHS U54 EB027049NIDA NIH HHS DP2 DA051912
6 · The paper itself

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein is the main antigen in all approved COVID-19 vaccines and is also the only target for monoclonal antibody (mAb) therapies. Immune responses to other viral antigens are generated after SARS-CoV-2 infection, but their contribution to the antiviral response remains unclear. Here, we interrogated whether nucleocapsid-specific antibodies can improve protection against SARS-CoV-2. We first immunized mice with a nucleocapsid-based vaccine and then transferred sera from these mice into naive mice, followed by challenge with SARS-CoV-2. We show that mice that received nucleocapsid-specific sera or a nucleocapsid-specific mAb exhibited enhanced control of SARS-CoV-2. Nucleocapsid-specific antibodies elicited NK-mediated, antibody-dependent cellular cytotoxicity (ADCC) against infected cells. To our knowledge, these findings provide the first demonstration in the coronavirus literature that antibody responses specific to the nucleocapsid protein can improve viral clearance, providing a rationale for the clinical evaluation of nucleocapsid-based mAb therapies to treat COVID-19.

Indexed as

Antibodies, MonoclonalCOVID-19NucleocapsidAnimalsAntibodies, ViralCOVID-19 VaccinesMiceSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, MonoclonalAntibodies, ViralCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Adaptive immunityCOVID-19Immunology

Identifiers

PMID36219482
PMCPMC9711872
OpenAlexW4304203302

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.