Evidence map›Paper›PMID 33318780›Full record

ArticleJournal of extracellular vesicles2020

Ivermectin inhibits extracellular vesicle secretion from parasitic nematodes.

Hannah J Loghry, Wang Yuan, Mostafa Zamanian, Nicolas J Wheeler, Timothy A Day, Michael J Kimber

Open access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.7field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Deep phenotypic profiling uncovers cryptic effects of antifilarial drugs.bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Impact of Ivermectin on the Gut Microbial Ecosystem.International journal of molecular sciences · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. A high-throughput sensory assay for parasitic and free-living nematodes.Integrative biology : quantitative biosciences from nano to macro · 2023
    Article
  11. Phenotypic Profiling of Macrocyclic Lactones on ParasiticAntimicrobial agents and chemotherapy · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Extracellular vesicles derived fromFrontiers in immunology · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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 at 2 institutions in 1 country.

Hannah J LoghryDepartment of Biomedical Sciences College of Veterinary Medicine Iowa State University Ames Iowa USA.
Wang YuanDepartment of Biomedical Sciences College of Veterinary Medicine Iowa State University Ames Iowa USA.
Mostafa ZamanianDepartment of Pathobiological Sciences University of Wisconsin-Madison Madison Wisconsin USA.
Nicolas J WheelerDepartment of Pathobiological Sciences University of Wisconsin-Madison Madison Wisconsin USA.
Timothy A DayDepartment of Biomedical Sciences College of Veterinary Medicine Iowa State University Ames Iowa USA.
Michael J KimberDepartment of Biomedical Sciences College of Veterinary Medicine Iowa State University Ames Iowa USA.
Iowa State University · USUniversity of Wisconsin–Madison · US

Funding

Molecular mechanisms controlling secretion in filarial nematode parasitesR01AI151171 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI Mostafa Zamanian · 2020 to 2026
$2.4M
Exploring the Structure and Function of Parasitic Nematode ExosomesR21AI117204 · NIAID · IOWA STATE UNIVERSITY · PI KIMBER, MICHAEL JOHN · 2016 to 2017
$403k
NIAID NIH HHS R01 AI151171NIAID NIH HHS R21 AI117204
6 · The paper itself

Abstract

Lymphatic filariasis (LF) is a disease caused by parasitic filarial nematodes that is endemic in 49 countries of the world and affects or threatens over 890 million people. Strategies to control LF rely heavily on mass administration of anthelmintic drugs including ivermectin (IVM), a macrocyclic lactone drug considered an Essential Medicine by the WHO. However, despite its widespread use the therapeutic mode of action of IVM against filarial nematodes is not clear. We have previously reported that filarial nematodes secrete extracellular vesicles (EVs) and that their cargo has immunomodulatory properties. Here we investigate the effects of IVM and other anti-filarial drugs on parasitic nematode EV secretion, motility, and protein secretion. We show that inhibition of EV secretion was a specific property of IVM, which had consistent and significant inhibitory effects across nematode life stages and species, with the exception of male parasites. IVM inhibited EV secretion, but not parasite motility, at therapeutically relevant concentrations. Protein secretion was inhibited by IVM in the microfilariae stage, but not in any other stage tested. Our data provides evidence that inhibiting the secretion of immunomodulatory EVs by parasitic nematodes could explain, at least in part, IVM mode of action and provides a phenotype for novel drug discovery.

Indexed as

AnimalsAntiparasitic AgentsBrugia malayiElephantiasis, FilarialExtracellular VesiclesFemaleGastrointestinal TractHelminth ProteinsIvermectinLocomotionMaleMicrofilariaePhagocytosisAntiparasitic AgentsHelminth ProteinsIvermectinBrugia malayiextracellular vesicleivermectinlymphatic filariasismacrocyclic lactoneparasite

Identifiers

PMID33318780
PMCPMC7726798
OpenAlexW3111432318

What OpenQuestion holds

Textmetadata
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.