Evidence map›Paper›PMID 25061263›Full record

ArticleMediators of inflammation2014

Genetic vaccination against experimental infection with myotropic parasite strains of Trypanosoma cruzi.

Adriano Fernando Araújo, Gabriel de Oliveira, Juliana Fraga Vasconcelos, Jonatan Ersching, Mariana Ribeiro Dominguez, José Ronnie Vasconcelos, Alexandre Vieira Machado, Ricardo Tostes Gazzinelli, Oscar Bruna-Romero, Milena Botelho Soares and 1 more

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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  6. Rapamycin Improves the Response of Effector and Memory CD8Frontiers in cellular and infection microbiology · 2021
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  7. Review
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  9. Review
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 4 institutions in 2 countries.

Adriano Fernando AraújoCentro de Terapia Celular e Molecular (CTCMol), Escola Paulista de Medicina, UNIFESP, Rua Mirassol, 207 04044-010 São Paulo, SP, Brazil ; Departmento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Mirassol, 207 04044-010 São Paulo, SP, Brazil.
Gabriel de OliveiraLaboratório Biologia Celular, Instituto Oswaldo Cruz (FIOCRUZ), Avenida Brasil, 4365-Manguinhos, 21040-360 Rio de Janeiro, RJ, Brazil.
Juliana Fraga VasconcelosCentro de Pesquisas Gonçalo Moniz, FIOCRUZ, Rua Waldemar Falcão, 121, 40296-710 Salvador, BA, Brazil ; Hospital São Rafael, Avenida São Rafael 2152, São Marcos, 41253-190 Salvador, BA, Brazil.
Jonatan ErschingCentro de Terapia Celular e Molecular (CTCMol), Escola Paulista de Medicina, UNIFESP, Rua Mirassol, 207 04044-010 São Paulo, SP, Brazil ; Departmento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Mirassol, 207 04044-010 São Paulo, SP, Brazil.
Mariana Ribeiro DominguezCentro de Terapia Celular e Molecular (CTCMol), Escola Paulista de Medicina, UNIFESP, Rua Mirassol, 207 04044-010 São Paulo, SP, Brazil ; Departmento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Mirassol, 207 04044-010 São Paulo, SP, Brazil.
José Ronnie VasconcelosCentro de Terapia Celular e Molecular (CTCMol), Escola Paulista de Medicina, UNIFESP, Rua Mirassol, 207 04044-010 São Paulo, SP, Brazil ; Departmento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Mirassol, 207 04044-010 São Paulo, SP, Brazil ; Departamento de Biociências, Instituto de Saúde e Sociedade, UNIFESP, Campus Baixada Santista, 11015-020 Santos, SP, Brazil.
Alexandre Vieira MachadoCentro de Pesquisas René Rachou, FIOCRUZ, Avenida Augusto de Lima 1.715, Barro Preto, 30190-002 Belo Horizonte, MG, Brazil.
Ricardo Tostes GazzinelliCentro de Pesquisas René Rachou, FIOCRUZ, Avenida Augusto de Lima 1.715, Barro Preto, 30190-002 Belo Horizonte, MG, Brazil ; Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Avenida Presidente Antônio Carlos, 6627, Pampulha, 31270-901 Belo Horizonte, MG, Brazil ; Division of Infectious Disease and Immunology, Department of Medicine, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA.
Oscar Bruna-RomeroDepartamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de Santa Catarina, Campus Universitário da Trindade, 88040-900 Florianopolis, SC, Brazil.
Milena Botelho SoaresCentro de Pesquisas Gonçalo Moniz, FIOCRUZ, Rua Waldemar Falcão, 121, 40296-710 Salvador, BA, Brazil ; Hospital São Rafael, Avenida São Rafael 2152, São Marcos, 41253-190 Salvador, BA, Brazil.
Mauricio Martins RodriguesCentro de Terapia Celular e Molecular (CTCMol), Escola Paulista de Medicina, UNIFESP, Rua Mirassol, 207 04044-010 São Paulo, SP, Brazil ; Departmento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Mirassol, 207 04044-010 São Paulo, SP, Brazil.
Universidade Federal de São Paulo · BRFundação Oswaldo Cruz · BRInstituto de Saúde · BRUniversidade Federal de Santa Catarina · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In earlier studies, we reported that a heterologous prime-boost regimen using recombinant plasmid DNA followed by replication-defective adenovirus vector, both containing Trypanosoma cruzi genes encoding trans-sialidase (TS) and amastigote surface protein (ASP) 2, provided protective immunity against experimental infection with a reticulotropic strain of this human protozoan parasite. Herein, we tested the outcome of genetic vaccination of F1 (CB10XBALB/c) mice challenged with myotropic parasite strains (Brazil and Colombian). Initially, we determined that the coadministration during priming of a DNA plasmid containing the murine IL-12 gene improved the immune response and was essential for protective immunity elicited by the heterologous prime-boost regimen in susceptible male mice against acute lethal infections with these parasites. The prophylactic or therapeutic vaccination of resistant female mice led to a drastic reduction in the number of inflammatory infiltrates in cardiac and skeletal muscles during the chronic phase of infection with either strain. Analysis of the electrocardiographic parameters showed that prophylactic vaccination reduced the frequencies of sinus arrhythmia and atrioventricular block. Our results confirmed that prophylactic vaccination using the TS and ASP-2 genes benefits the host against acute and chronic pathologies caused by T. cruzi and should be further evaluated for the development of a veterinary or human vaccine against Chagas disease.

Indexed as

AnimalsCD8-Positive T-LymphocytesChagas DiseaseFemaleGlycoproteinsInterleukin-12MaleMiceMice, Inbred BALB CNeuraminidaseTrypanosoma cruziASP-2 protein, Trypanosoma cruziGlycoproteinsInterleukin-12Neuraminidasetrans-sialidase

Identifiers

PMID25061263
PMCPMC4098640
OpenAlexW2098017361

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.