Evidence map›Paper›PMID 27635405›Full record

ReviewJournal of immunology research2016

Schistosome-Derived Molecules as Modulating Actors of the Immune System and Promising Candidates to Treat Autoimmune and Inflammatory Diseases.

Luis Janssen, Gisele Lorranna Silva Santos, Herick Sampaio Muller, Anderson Rodrigues Araújo Vieira, Tatiana Amabile de Campos, Vicente de Paulo Martins

Abstract readReview
In one paragraph

Review in Journal of immunology research, 2016. 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.

  1. Article
  2. Oxidative Stress and Cancer Risk in Schistosomiasis.Oxidative medicine and cellular longevity · 2024
    Review
  3. Article
  4. Review
  5. Schistosome immunomodulators.PLoS pathogens · 2021
    Review
  6. Review
  7. Review
  8. Article
  9. Allergen-Specific Treg Cells Upregulated by Lung-StageFrontiers in cell and developmental biology · 2021
    Article
  10. Article
  11. Article
  12. Review
  13. 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

6 authors.

Luis JanssenDepartamento de Biologia Celular, Instituto de Ciências Biológicas, Universidade de Brasília, 70910-900 Brasília, DF, Brazil; Programa de Pós-Graduação em Biologia Molecular, Universidade de Brasília, 70910-900 Brasília, DF, Brazil.ORCID 0000-0002-5772-0477
Gisele Lorranna Silva SantosDepartamento de Biologia Celular, Instituto de Ciências Biológicas, Universidade de Brasília, 70910-900 Brasília, DF, Brazil; Programa de Pós-Graduação em Medicina Tropical, Universidade de Brasília, 70910-900 Brasília, DF, Brazil.ORCID 0000-0002-8430-0232
Herick Sampaio MullerDepartamento de Biologia Celular, Instituto de Ciências Biológicas, Universidade de Brasília, 70910-900 Brasília, DF, Brazil; Programa de Pós-Graduação em Patologia Molecular, Universidade de Brasília, 70910-900 Brasília, DF, Brazil.ORCID 0000-0003-2474-8294
Anderson Rodrigues Araújo VieiraDepartamento de Biologia Celular, Instituto de Ciências Biológicas, Universidade de Brasília, 70910-900 Brasília, DF, Brazil; Programa de Pós-Graduação em Biologia Microbiana, Universidade de Brasília, 70910-900 Brasília, DF, Brazil.
Tatiana Amabile de CamposDepartamento de Biologia Celular, Instituto de Ciências Biológicas, Universidade de Brasília, 70910-900 Brasília, DF, Brazil; Programa de Pós-Graduação em Biologia Microbiana, Universidade de Brasília, 70910-900 Brasília, DF, Brazil.
Vicente de Paulo MartinsDepartamento de Biologia Celular, Instituto de Ciências Biológicas, Universidade de Brasília, 70910-900 Brasília, DF, Brazil; Programa de Pós-Graduação em Biologia Molecular, Universidade de Brasília, 70910-900 Brasília, DF, Brazil; Programa de Pós-Graduação em Medicina Tropical, Universidade de Brasília, 70910-900 Brasília, DF, Brazil.ORCID 0000-0001-7611-861X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is long known that some parasite infections are able to modulate specific pathways of host's metabolism and immune responses. This modulation is not only important in order to understand the host-pathogen interactions and to develop treatments against the parasites themselves but also important in the development of treatments against autoimmune and inflammatory diseases. Throughout the life cycle of schistosomes the mammalian hosts are exposed to several biomolecules that are excreted/secreted from the parasite infective stage, named cercariae, from their tegument, present in adult and larval stages, and finally from their eggs. These molecules can induce the activation and modulation of innate and adaptive responses as well as enabling the evasion of the parasite from host defense mechanisms. Immunomodulatory effects of helminth infections and egg molecules are clear, as well as their ability to downregulate proinflammatory cytokines, upregulate anti-inflammatory cytokines, and drive a Th2 type of immune response. We believe that schistosomes can be used as a model to understand the potential applications of helminths and helminth-derived molecules against autoimmune and inflammatory diseases.

Indexed as

Host-Parasite InteractionsAnimalsAntigens, HelminthAutoimmune DiseasesDisease Models, AnimalHelminthsHost-Pathogen InteractionsHumansImmunomodulationInflammationLife Cycle StagesSchistosomaAntigens, Helminth

Identifiers

PMID27635405
PMCPMC5011209

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.