Evidence map›Paper›PMID 27030586›Full record

ArticleClinical and vaccine immunology : CVI2016

Production of a Recombinant Dengue Virus 2 NS5 Protein and Potential Use as a Vaccine Antigen.

Rúbens Prince Dos Santos Alves, Lennon Ramos Pereira, Denicar Lina Nascimento Fabris, Felipe Scassi Salvador, Robert Andreata Santos, Paolo Marinho de Andrade Zanotto, Camila Malta Romano, Jaime Henrique Amorim, Luís Carlos de Souza Ferreira

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-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

25 citing papers in PubMed, 39 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

9 authors at 2 institutions in 1 country.

Rúbens Prince Dos Santos AlvesLaboratório de Desenvolvimento de Vacinas, Instituto de Ciências Biomédicas, Departamento de Microbiologia, Universidade de São Paulo, São Paulo, Brazil.
Lennon Ramos PereiraLaboratório de Desenvolvimento de Vacinas, Instituto de Ciências Biomédicas, Departamento de Microbiologia, Universidade de São Paulo, São Paulo, Brazil.
Denicar Lina Nascimento FabrisLaboratório de Desenvolvimento de Vacinas, Instituto de Ciências Biomédicas, Departamento de Microbiologia, Universidade de São Paulo, São Paulo, Brazil.
Felipe Scassi SalvadorInstituto de Medicina Tropical, Escola de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Robert Andreata SantosLaboratório de Desenvolvimento de Vacinas, Instituto de Ciências Biomédicas, Departamento de Microbiologia, Universidade de São Paulo, São Paulo, Brazil.
Paolo Marinho de Andrade ZanottoLaboratório de Evolução Molecular e Bioinformática, Instituto de Ciências Biomédicas, Departamento de Microbiologia, Universidade de São Paulo, São Paulo, Brazil.
Camila Malta RomanoInstituto de Medicina Tropical, Escola de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Jaime Henrique AmorimLaboratório de Desenvolvimento de Vacinas, Instituto de Ciências Biomédicas, Departamento de Microbiologia, Universidade de São Paulo, São Paulo, Brazil jaime.amorim@ufob.edu.br lcsf@usp.br.
Luís Carlos de Souza FerreiraLaboratório de Desenvolvimento de Vacinas, Instituto de Ciências Biomédicas, Departamento de Microbiologia, Universidade de São Paulo, São Paulo, Brazil jaime.amorim@ufob.edu.br lcsf@usp.br.
Universidade de São Paulo · BRInstituto de Medicina Avançada · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue fever is caused by any of the four known dengue virus serotypes (DENV1 to DENV4) that affect millions of people worldwide, causing a significant number of deaths. There are vaccines based on chimeric viruses, but they still are not in clinical use. Anti-DENV vaccine strategies based on nonstructural proteins are promising alternatives to those based on whole virus or structural proteins. The DENV nonstructural protein 5 (NS5) is the main target of anti-DENV T cell-based immune responses in humans. In this study, we purified a soluble recombinant form of DENV2 NS5 expressed in Escherichia coli at large amounts and high purity after optimization of expression conditions and purification steps. The purified DENV2 NS5 was recognized by serum from DENV1-, DENV2-, DENV3-, or DENV4-infected patients in an epitope-conformation-dependent manner. In addition, immunization of BALB/c mice with NS5 induced high levels of NS5-specific antibodies and expansion of gamma interferon- and tumor necrosis factor alpha-producing T cells. Moreover, mice immunized with purified NS5 were partially protected from lethal challenges with the DENV2 NGC strain and with a clinical isolate (JHA1). These results indicate that the recombinant NS5 protein preserves immunological determinants of the native protein and is a promising vaccine antigen capable of inducing protective immune responses.

Indexed as

AnimalsAntibodies, ViralComputer SimulationDengueDengue VaccinesDengue VirusEpitopesEscherichia coliHumansImmunity, CellularMiceMice, Inbred BALB CRecombinant ProteinsViral Nonstructural ProteinsAntibodies, ViralDengue VaccinesEpitopesNS5 protein, dengue virusRecombinant ProteinsViral Nonstructural Proteins

Identifiers

PMID27030586
PMCPMC4895003
OpenAlexW2322022606

What OpenQuestion holds

Textmetadata
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.