Evidence map›Paper›PMID 30285837›Full record

ReviewParasites & vectors2018

Leishmaniasis and glycosaminoglycans: a future therapeutic strategy?

Débora Almeida Merida-de-Barros, Suzana Passos Chaves, Celso Luis Ribeiro Belmiro, João Luiz Mendes Wanderley

Abstract readReview
In one paragraph

Review in Parasites & vectors, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Journal of parasitic diseases : official organ of the Indian Society for Parasitology · 2024
    Review
  3. Review
  4. Review
  5. Roles of extracellular matrix in lung diseases.Fukushima journal of medical science · 2024
    Review
  6. Integrated Omics Reveal the Pathogenic Potential ofTransboundary and emerging diseases · 2024
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Glycosaminoglycan-Protein Interactions: The First Draft of the Glycosaminoglycan Interactome.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Review
  12. Glycosaminoglycans: Sweet as Sugar Targets for Topical Skin Anti-Aging.Clinical, cosmetic and investigational dermatology · 2021
    Review
  13. Article
  14. Article
  15. 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

4 authors.

Débora Almeida Merida-de-BarrosLaboratório de Imunoparasitologia, Unidade Integrada de Pesquisa em Produtos Bioativos e Biociências, Campus UFRJ-Macaé, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Suzana Passos ChavesLaboratório de Imunoparasitologia, Unidade Integrada de Pesquisa em Produtos Bioativos e Biociências, Campus UFRJ-Macaé, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Celso Luis Ribeiro BelmiroLaboratório de Imunoparasitologia, Unidade Integrada de Pesquisa em Produtos Bioativos e Biociências, Campus UFRJ-Macaé, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
João Luiz Mendes WanderleyLaboratório de Imunoparasitologia, Unidade Integrada de Pesquisa em Produtos Bioativos e Biociências, Campus UFRJ-Macaé, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil. lmwjoao@macae.ufrj.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leishmania spp. depend on effective macrophage infection to establish and develop in mammalian hosts. Both metacyclic promastigotes and amastigotes are able to infect host cells, and thus they rely on several ligands that, when recognized by macrophage receptors, mediate parasite uptake. During macrophage primary infection with metacyclic forms from the insect vector and during amastigote dissemination via macrophage rupture, both infective stages have to cope with the host extracellular microenvironment, including extracellular matrix molecules. Glycosaminoglycans are abundant in the extracellular matrix and many of these molecules are able to interact with the parasite and the host cell, mediating positive and negative effects for the infection, depending on their structure and/or location. In addition, glycosaminoglycans are present at the surface of macrophages as proteoglycans, playing important roles for parasite recognition and uptake. In this review, we discuss glycosaminoglycans in the context of Leishmania infection as well as the possible applications of the current knowledge regarding these molecules for the development of new therapeutic strategies to control parasite dissemination.

Indexed as

AnimalsCell Adhesion MoleculesGlycoconjugatesGlycosaminoglycansHost-Parasite InteractionsHumansLeishmaniaLeishmaniasisMacrophagesProteoglycansCell Adhesion MoleculesGlycoconjugatesGlycosaminoglycansheparin-binding protein (Leishmania)ProteoglycansGlycosaminoglycansLeishmaniaMacrophageReceptors

Identifiers

PMID30285837
PMCPMC6171297

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.