Evidence map›Paper›PMID 39702529›Full record

ArticleNPJ vaccines2024

Co-immunization with spike and nucleocapsid based DNA vaccines for long-term protective immunity against SARS-CoV-2 Omicron.

Paolla Beatriz Almeida Pinto, Julia Timis, Kantinan Chuensirikulchai, Qin Hui Li, Hsueh Han Lu, Erin Maule, Michael Nguyen, Rúbens Prince Dos Santos Alves, Shailendra Kumar Verma, Fernanda Ana-Sosa-Batiz and 8 more

Abstract read
In one paragraph

Article in NPJ vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
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  5. 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.

Paolla Beatriz Almeida PintoCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Julia TimisCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Kantinan ChuensirikulchaiCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Qin Hui LiCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.ORCID http://orcid.org/0000-0002-2792-9018
Hsueh Han LuCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.ORCID http://orcid.org/0000-0002-0832-9607
Erin MauleCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Michael NguyenCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Rúbens Prince Dos Santos AlvesCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Shailendra Kumar VermaCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.ORCID http://orcid.org/0000-0001-9142-3022
Fernanda Ana-Sosa-BatizCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Kristen ValentineCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Sara Landeras-BuenoCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Kenneth KimCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Kathryn HastieCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.
Erica Ollmann SaphireCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA.ORCID http://orcid.org/0000-0002-1206-7451
Ada AlvesLaboratory of Biotechnology and Physiology of Viral Infections, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, 21040-900, Brazil.
Annie Elong NgonoCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA. aelong@lji.org.
Sujan ShrestaCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, 92037, USA. sujan@lji.org.ORCID http://orcid.org/0000-0003-2906-8474

Funding

Specific and Broadly Active Monoclonal Antibody Therapeutics Against The FilovirusesU19AI142790 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SAPHIRE, ERICA OLLMANN · 2019 to 2023
$40.0M
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brazilian Federal Agency for the Support and Evaluation of Graduate Education) 88887.472772/2019-00Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brazilian Federal Agency for the Support and Evaluation of Graduate Education) 88887.583319/2020-00Division of Intramural Research, National Institute of Allergy and Infectious Diseases (Division of Intramural Research of the NIAID) U19 AI142790-02S1Division of Intramural Research, National Institute of Allergy and Infectious Diseases (Division of Intramural Research of the NIAID) U19 AI142790-02S1uniNIAID NIH HHS U19 AI142790
6 · The paper itself

Abstract

The continuing evolution of SARS-CoV-2 variants challenges the durability of existing spike (S)-based COVID-19 vaccines. We hypothesized that vaccines composed of both S and nucleocapsid (N) antigens would increase the durability of protection by strengthening and broadening cellular immunity compared with S-based vaccines. To test this, we examined the immunogenicity and efficacy of wild-type SARS-CoV-2 S- and N-based DNA vaccines administered individually or together to K18-hACE2 mice. S, N, and S + N vaccines all elicited polyfunctional CD4

Identifiers

PMID39702529
PMCPMC11659323

What OpenQuestion holds

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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.