Evidence map›Paper›PMID 28871190›Full record

ArticleScientific reports2017

New insights about functional and cross-reactive properties of antibodies generated against recombinant TbpBs of Haemophilus parasuis.

Bibiana Martins Barasuol, João Antônio Guizzo, Jamie Elisabeth Fegan, Sonia Martínez-Martínez, Elías Fernando Rodríguez-Ferri, César Bernardo Gutiérrez-Martín, Luiz Carlos Kreutz, Anthony Bernard Schryvers, Rafael Frandoloso

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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  6. TbpBPathogens (Basel, Switzerland) · 2022
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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.

Bibiana Martins BarasuolLaboratory of Microbiology and Advanced Immunology, Faculty of Agronomy and Veterinary Medicine, University of Passo Fundo, Passo Fundo, 99052-900, Brazil.
João Antônio GuizzoLaboratory of Microbiology and Advanced Immunology, Faculty of Agronomy and Veterinary Medicine, University of Passo Fundo, Passo Fundo, 99052-900, Brazil.
Jamie Elisabeth FeganDepartment of Microbiology & Infectious Diseases, Faculty of Medicine, University of Calgary, Calgary, T2N 4N1, Alberta, Canada.
Sonia Martínez-MartínezUnidad de Microbiología e Inmunología, Departamento de Sanidad Animal, Facultad de Veterinaria, Universidad de León, 24007, León, Spain.
Elías Fernando Rodríguez-FerriUnidad de Microbiología e Inmunología, Departamento de Sanidad Animal, Facultad de Veterinaria, Universidad de León, 24007, León, Spain.
César Bernardo Gutiérrez-MartínUnidad de Microbiología e Inmunología, Departamento de Sanidad Animal, Facultad de Veterinaria, Universidad de León, 24007, León, Spain.
Luiz Carlos KreutzLaboratory of Microbiology and Advanced Immunology, Faculty of Agronomy and Veterinary Medicine, University of Passo Fundo, Passo Fundo, 99052-900, Brazil.
Anthony Bernard SchryversDepartment of Microbiology & Infectious Diseases, Faculty of Medicine, University of Calgary, Calgary, T2N 4N1, Alberta, Canada.
Rafael FrandolosoLaboratory of Microbiology and Advanced Immunology, Faculty of Agronomy and Veterinary Medicine, University of Passo Fundo, Passo Fundo, 99052-900, Brazil. rfran@upf.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vaccines have become fundamental in the control and elimination of Glässer Disease, a systemic disease of pigs caused by Haemophilus parasuis. The classic vaccines available for prevention of this infection were developed without a robust knowledge about host immunological mechanisms. In this study, we demonstrated the presence of cross-reactive epitopes on both the N-lobe and C-lobe of variants of transferrin binding protein B (TbpBs) expressed on the surface of 6 virulent serovars of H. parasuis. Antibodies against TbpB-derived antigens were capable of increasing the phagocytic capacity of neutrophils and were also capable of blocking porcine transferrin from binding to TbpB. Surprisingly, none of the pig or mice antisera from animals immunized with TbpB-derived antigens mixed with Montanide IMS 2215 VG PR adjuvant were able to activate the classical complement pathway (CCP). In contrast, antisera from mice immunized with TbpB-derived antigens adjuvanted with Freund's adjuvants or Montanide Gel 01 were able to activate the CCP and kill H. parasuis. Our results demonstrate that the type of adjuvant can modulate the functional response induced by TbpB-derived antigens. Based on these results, we propose that a properly formulated TbpB-based vaccine may elicit a functional protective antibody response with broad cross-reactivity against heterologous strains of H. parasuis.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, BacterialCross ReactionsEpitopesHaemophilus InfectionsHaemophilus parasuisHaemophilus VaccinesRecombinant ProteinsSwineSwine DiseasesTransferrinTransferrin-Binding Protein BVirulenceAdjuvants, ImmunologicAntibodies, BacterialEpitopesHaemophilus VaccinesRecombinant ProteinsTransferrinTransferrin-Binding Protein B

Identifiers

PMID28871190
PMCPMC5583350

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Registered trials

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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.