Evidence map›Paper›PMID 32221951›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2020

Establishment of a Standardized Vaccine Protocol for the Analysis of Protective Immune Responses During Experimental Trypanosome Infections in Mice.

Magdalena Radwanska, Hang Thi Thu Nguyen, Sangphil Moon, Emmanuel Obishakin, Stefan Magez

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

5 authors at 4 institutions in 3 countries.

Magdalena RadwanskaBiomedical Research Centre, Department of Environmental Technology, Food Technology and Molecular Biotechnology, Ghent University, Incheon, South Korea.
Hang Thi Thu NguyenBiomedical Research Centre, Department of Environmental Technology, Food Technology and Molecular Biotechnology, Ghent University, Incheon, South Korea.
Sangphil MoonBiomedical Research Centre, Department of Environmental Technology, Food Technology and Molecular Biotechnology, Ghent University, Incheon, South Korea.
Emmanuel ObishakinBiomedical Research Centre, Department of Environmental Technology, Food Technology and Molecular Biotechnology, Ghent University, Incheon, South Korea.
Stefan MagezBiomedical Research Centre, Department of Environmental Technology, Food Technology and Molecular Biotechnology, Ghent University, Incheon, South Korea. stefan.magez@ghent.ac.kr.
Vrije Universiteit Brussel · BEGhent University · BEGhent University Global Campus · KRNational Veterinary Research Institute · NG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To date, trypanosomosis control in humans and animals is achieved by a combination of parasitological screening and treatment. While this approach has successfully brought down the number of reported T. b. gambiense Human African Trypanosomosis (HAT) cases, the method does not offer a sustainable solution for animal trypanosomosis (AT). The main reasons for this are (i) the worldwide distribution of AT, (ii) the wide range of insect vectors involved in transmission of AT, and (iii) the existence of a wildlife parasite reservoir that can serve as a source for livestock reinfection. Hence, in order to control livestock trypanosomosis the only viable long-term solution is an effective antitrypanosome vaccination strategy. Over the last decades, multiple vaccine approaches have been proposed. Despite repeated reports of promising experimental approaches, none of those made it to a field applicable vaccine format. This failure can in part be attributed to flaws in the experimental design that favor a positive laboratory result. This chapter provides a vaccine protocol that should allow for a proper outcome prediction in experimental anti-AT vaccine approaches.

Indexed as

AnimalsDisease Models, AnimalLivestockMiceProtozoan VaccinesResearch DesignTrypanosoma brucei gambienseTrypanosomiasis, AfricanVaccinationProtozoan VaccinesB cellMemoryVaccination

Identifiers

PMID32221951
OpenAlexW3013547863

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.