Evidence map›Paper›PMID 30384424›Full record

ArticleViruses2018

Immunogenicity of Pigeon Circovirus Recombinant Capsid Protein in Pigeons.

Tomasz Stenzel, Daria Dziewulska, Bartłomiej Tykałowski, Marcin Śmiałek, Joanna Kowalczyk, Andrzej Koncicki

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 29 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

6 authors at 1 institution in 1 country.

Tomasz StenzelDepartment of Poultry Diseases, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, ul. Oczapowskiego 13, 10-719 Olsztyn, Poland. tomasz.stenzel@uwm.edu.pl.ORCID 0000-0001-6268-9841
Daria DziewulskaDepartment of Poultry Diseases, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, ul. Oczapowskiego 13, 10-719 Olsztyn, Poland. daria.pestka@uwm.edu.pl.ORCID 0000-0001-6425-1202
Bartłomiej TykałowskiDepartment of Poultry Diseases, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, ul. Oczapowskiego 13, 10-719 Olsztyn, Poland. bartlomiej.tykalowski@uwm.edu.pl.ORCID 0000-0002-4711-1619
Marcin ŚmiałekDepartment of Poultry Diseases, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, ul. Oczapowskiego 13, 10-719 Olsztyn, Poland. marcin.smialek@uwm.edu.pl.
Joanna KowalczykDepartment of Poultry Diseases, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, ul. Oczapowskiego 13, 10-719 Olsztyn, Poland. welencasia@gmail.com.
Andrzej KoncickiDepartment of Poultry Diseases, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, ul. Oczapowskiego 13, 10-719 Olsztyn, Poland. koncicki@uwm.edu.pl.
University of Warmia and Mazury in Olsztyn · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pigeon circovirus (PiCV) is the most frequently diagnosed virus in pigeons and is thought to be one of the causative factors of a complex disease called the young pigeon disease syndrome (YPDS). The development of a vaccine against this virus could be a strategy for YPDS control. Since laboratory culture of PiCV is impossible, its recombinant capsid protein (rCP) can be considered as a potential antigen candidate in sub-unit vaccines. The aim of this basic research was to evaluate the immune response of pigeons to PiCV rCP. Sixty six-week-old carrier pigeons were divided into two groups (experimental immunized with PiCV rCP mixed with an adjuvant, and control immunized with an adjuvant only), and immunized twice in a 21-day interval. On the day of immunization and on two, 23, 39, and 46 days post first immunization (dpv), samples of blood, spleen, and bursa of Fabricius were collected from six birds from each group to examine anti-PiCV rCP IgY, anti-PiCV rCP IgY-secreting B cells (SBC), IFN-γ gene expression, and percentage of T CD3⁺, CD4⁺, CD8⁺, and B IgM⁺ lymphocytes. The results indicated a correct immune response to PiCV rCP both in humoral and cell-mediated immunity, which was manifested by seroconversion since 23 dpv, by a significantly higher anti-PiCV rCP IgY-SBC number on two and 23 dpv, and significantly higher IFN-γ gene expression since two dpv. There were no significant differences or trends noted between particular T and B lymphocyte subpopulations. To conclude, PiCV rCP may be deemed immunogenic and could be considered as an antigen candidate in sub-unit vaccines against PiCV infections in pigeons.

Indexed as

AnimalsBird DiseasesCapsid ProteinsCircoviridae InfectionsCircovirusColumbidaeEnzyme-Linked Immunosorbent AssayEnzyme-Linked Immunospot AssayFlow CytometryHost-Pathogen InteractionsImmunityImmunoglobulin MImmunoglobulinsInterferon-gammaRecombinant ProteinsT-Lymphocyte SubsetsCapsid ProteinsIgYImmunoglobulin MImmunoglobulinsInterferon-gammaRecombinant ProteinsELISAELISPOTflow cytometryIFN-γ gene expressionpigeon circovirusrecombinant capsid proteinvaccination

Identifiers

PMID30384424
PMCPMC6265742
OpenAlexW2898772375

What OpenQuestion holds

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LicenceCC BY
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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.