Evidence map›Paper›PMID 28594938›Full record

ReviewPLoS neglected tropical diseases2017

The enemy within: Targeting host-parasite interaction for antileishmanial drug discovery.

Suzanne Lamotte, Gerald F Späth, Najma Rachidi, Eric Prina

Abstract readReview
In one paragraph

Review in PLoS neglected tropical diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Leishmanicidal Activity of Guanidine Derivatives againstTropical medicine and infectious disease · 2023
    Article
  9. Review
  10. A determination of pan-pathogen antimicrobials?Medicine in drug discovery · 2022
    Review
  11. Comparison of high throughput RNA sequences betweenFrontiers in cellular and infection microbiology · 2022
    Article
  12. Proteomic Analysis ofPathogens (Basel, Switzerland) · 2021
    Article
  13. Article
  14. Identification of the Host Substratome ofFrontiers in cell and developmental biology · 2021
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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.

Suzanne LamotteInstitut Pasteur and INSERM U1201, Unité de Parasitologie Moléculaire et Signalisation, Paris, France.ORCID http://orcid.org/0000-0003-2699-7219
Gerald F SpäthInstitut Pasteur and INSERM U1201, Unité de Parasitologie Moléculaire et Signalisation, Paris, France.
Najma RachidiInstitut Pasteur and INSERM U1201, Unité de Parasitologie Moléculaire et Signalisation, Paris, France.
Eric PrinaInstitut Pasteur and INSERM U1201, Unité de Parasitologie Moléculaire et Signalisation, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The state of antileishmanial chemotherapy is strongly compromised by the emergence of drug-resistant Leishmania. The evolution of drug-resistant phenotypes has been linked to the parasites' intrinsic genome instability, with frequent gene and chromosome amplifications causing fitness gains that are directly selected by environmental factors, including the presence of antileishmanial drugs. Thus, even though the unique eukaryotic biology of Leishmania and its dependence on parasite-specific virulence factors provide valid opportunities for chemotherapeutical intervention, all strategies that target the parasite in a direct fashion are likely prone to select for resistance. Here, we review the current state of antileishmanial chemotherapy and discuss the limitations of ongoing drug discovery efforts. We finally propose new strategies that target Leishmania viability indirectly via mechanisms of host-parasite interaction, including parasite-released ectokinases and host epigenetic regulation, which modulate host cell signaling and transcriptional regulation, respectively, to establish permissive conditions for intracellular Leishmania survival.

Indexed as

AnimalsAntiprotozoal AgentsDrug DiscoveryDrug ResistanceEpigenesis, GeneticHost-Parasite InteractionsHumansLeishmaniaLeishmaniasisMacrophagesMiceAntiprotozoal Agents

Identifiers

PMID28594938
PMCPMC5464532

What OpenQuestion holds

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LicenceCC BY
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.