Evidence map›Paper›PMID 34993638›Full record

ReviewParasitology research2022

Selenium and protozoan parasitic infections: selenocompounds and selenoproteins potential.

Sajad Rashidi, Celia Fernández-Rubio, Reza Mansouri, Mohammad Ali-Hassanzadeh, Esmaeel Ghani, Mohammadreza Karimazar, Raúl Manzano-Román, Paul Nguewa

Abstract readReview
In one paragraph

Review in Parasitology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. "Alphabet" Selenoproteins: Implications in Pathology.International journal of molecular sciences · 2023
    Review
  5. Article
  6. Article
  7. 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

8 authors.

Sajad Rashidi *Department of Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Celia Fernández-Rubio *ISTUN Institute of Tropical Health, Department of Microbiology and Parasitology. IdiSNA (Navarra Institute for Health Research), University of Navarra, c/ Irunlarrea 1, 31008, Pamplona, Spain.
Reza MansouriDepartment of Immunology, Faculty of Medicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran.
Mohammad Ali-HassanzadehDepartment of Immunology, School of Medicine, Jiroft University of Medical Sciences, Jiroft, Iran.
Esmaeel GhaniEndocrinology and Metabolism Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
Mohammadreza KarimazarDepartment of Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Raúl Manzano-RománInfectious and Tropical Diseases Group (E-INTRO), Institute of Biomedical Research of Salamanca-Research Center for Tropical Diseases at the University of Salamanca (IBSAL-CIETUS), Faculty of Pharmacy, University of Salamanca, 37008, Salamanca, Spain. rmanzano@usal.es.ORCID http://orcid.org/0000-0002-5066-9496
Paul NguewaISTUN Institute of Tropical Health, Department of Microbiology and Parasitology. IdiSNA (Navarra Institute for Health Research), University of Navarra, c/ Irunlarrea 1, 31008, Pamplona, Spain. panguewa@unav.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current drug treatments against protozoan parasitic diseases including Chagas, malaria, leishmaniasis, and toxoplasmosis represent good examples of drug resistance mechanisms and have shown diverse side effects. Therefore, the identification of novel therapeutic strategies and drug compounds against such life-threatening diseases is urgent. According to the successful usage of selenium (Se) compounds-based therapy against some diseases, this therapeutic strategy has been recently further underlined against these parasitic diseases by targeting different parasite´s essential pathways. On the other hand, due to the important functions played by parasite selenoproteins in their biology (such as modulating the host immune response), they can be also considered as a novel therapeutic strategy by designing specific inhibitors against these important proteins. In addition, the immunomodulatory potentiality of these compounds to trigger T helper type 1 (Th1) cells and cytokine-mediated immune response for the substantial induction of proinflammatory cytokines, thus, Se, selenoproteins, and parasite selenoproteins could be further investigated to find possible vaccine antigens. Herein, we collect and present the results of some studies regarding Se-based therapy against protozoan parasitic diseases and highlight relevant information and some viewpoints that might be insightful to advance toward more effective studies in the future.

Indexed as

Immunity, CellularSeleniumSelenoproteinsAnimalsHumansProtozoan InfectionsSeleniumSelenoproteinsProtozoan parasitic diseasesSeleniumSe-nanoparticlesSe supplementationTherapy

Identifiers

PMID34993638
PMCPMC8735723

What OpenQuestion holds

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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.