Evidence map›Paper›PMID 25700363›Full record

ArticlePLoS neglected tropical diseases2015

Repurposing auranofin as a lead candidate for treatment of lymphatic filariasis and onchocerciasis.

Christina A Bulman, Chelsea M Bidlow, Sara Lustigman, Fidelis Cho-Ngwa, David Williams, Alberto A Rascón, Nancy Tricoche, Moses Samje, Aaron Bell, Brian Suzuki and 15 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

60 citing papers in PubMed, 106 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. Old drugs, new weapons: current trends in repurposing therapies against antimicrobial resistance.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Aspartyl Protease Inhibitors as Anti-Filarial Drugs.Pathogens (Basel, Switzerland) · 2022
    Article
  16. Article
  17. Review
  18. Article
  19. Anti-Onchocercal Properties of Extracts ofJournal of tropical medicine · 2022
    Article
  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

25 authors at 9 institutions in 2 countries.

Christina A BulmanCenter for Discovery and Innovation in Parasitic Diseases, University of California San Francisco, San Francisco, California, United States of America.
Chelsea M BidlowCenter for Discovery and Innovation in Parasitic Diseases, University of California San Francisco, San Francisco, California, United States of America.
Sara LustigmanLindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.
Fidelis Cho-NgwaDepartment of Biochemistry and Molecular Biology, University of Buea, Buea, SW Region, Cameroon.
David WilliamsDepartment of Immunology and Microbiology, Rush University Medical Center, Chicago, Illinois, United States of America.
Alberto A RascónCenter for Discovery and Innovation in Parasitic Diseases, University of California San Francisco, San Francisco, California, United States of America; Department of Chemistry, San Jose State University, San Jose, California, United States of America.
Nancy TricocheLindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.
Moses SamjeDepartment of Biochemistry and Molecular Biology, University of Buea, Buea, SW Region, Cameroon.
Aaron BellLindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.
Brian SuzukiCenter for Discovery and Innovation in Parasitic Diseases, University of California San Francisco, San Francisco, California, United States of America.
K C LimCenter for Discovery and Innovation in Parasitic Diseases, University of California San Francisco, San Francisco, California, United States of America.
Nonglak SupakorndejFilariaTech, Athens, Georgia, United States of America.
Prasit SupakorndejDepartment of Infectious Diseases, University of Georgia, Athens, Georgia, United States of America.
Alan R WolfeDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, California, United States of America.
Giselle M KnudsenUCSF Mass Spectrometry Facility, Department of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, California, United States of America.
Steven ChenSmall Molecule Discovery Center, University of California San Francisco, San Francisco, California, United States of America.
Chris WilsonSmall Molecule Discovery Center, University of California San Francisco, San Francisco, California, United States of America.
Kean-Hooi AngSmall Molecule Discovery Center, University of California San Francisco, San Francisco, California, United States of America.
Michelle ArkinSmall Molecule Discovery Center, University of California San Francisco, San Francisco, California, United States of America.
Jiri GutCenter for Discovery and Innovation in Parasitic Diseases, University of California San Francisco, San Francisco, California, United States of America.
Chris FranklinCenter for Discovery and Innovation in Parasitic Diseases, University of California San Francisco, San Francisco, California, United States of America.
Chris MarcellinoCase Western Reserve University School of Medicine, Cleveland, Ohio, United States of America.
James H McKerrowSkaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, San Diego, California, United States of America.
Anjan DebnathSkaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, San Diego, California, United States of America.
Judy A SakanariCenter for Discovery and Innovation in Parasitic Diseases, University of California San Francisco, San Francisco, California, United States of America.
University of California, San Francisco · USCenter for Discovery · USNew York Blood Center · USUniversity of Buea · CMRush University Medical Center · USUniversity of California, San Diego · USUniversity of Georgia · USUniversity of Montana · USUniversity School · US

Funding

Bio-Organic Biomedical Mass Spectromy ResourceP41GM103481 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BURLINGAME, ALMA L · 2012 to 2015
$6.4M
NIGMS NIH HHS GM103481NIGMS NIH HHS P41 GM103481
6 · The paper itself

Abstract

Two major human diseases caused by filariid nematodes are onchocerciasis, or river blindness, and lymphatic filariasis, which can lead to elephantiasis. The drugs ivermectin, diethylcarbamazine (DEC), and albendazole are used in control programs for these diseases, but are mainly effective against the microfilarial stage and have minimal or no effect on adult worms. Adult Onchocerca volvulus and Brugia malayi worms (macrofilariae) can live for up to 15 years, reproducing and allowing the infection to persist in a population. Therefore, to support control or elimination of these two diseases, effective macrofilaricidal drugs are necessary, in addition to current drugs. In an effort to identify macrofilaricidal drugs, we screened an FDA-approved library with adult worms of Brugia spp. and Onchocerca ochengi, third-stage larvae (L3s) of Onchocerca volvulus, and the microfilariae of both O. ochengi and Loa loa. We found that auranofin, a gold-containing drug used for rheumatoid arthritis, was effective in vitro in killing both Brugia spp. and O. ochengi adult worms and in inhibiting the molting of L3s of O. volvulus with IC50 values in the low micromolar to nanomolar range. Auranofin had an approximately 43-fold higher IC50 against the microfilariae of L. loa compared with the IC50 for adult female O. ochengi, which may be beneficial if used in areas where Onchocerca and Brugia are co-endemic with L. loa, to prevent severe adverse reactions to the drug-induced death of L. loa microfilariae. Further testing indicated that auranofin is also effective in reducing Brugia adult worm burden in infected gerbils and that auranofin may be targeting the thioredoxin reductase in this nematode.

Indexed as

AdultAlbendazoleAnimalsAnthelminticsAuranofinBrugia malayiCattleCell LineDiethylcarbamazineDrug RepositioningElephantiasis, FilarialFemaleFilaricidesGerbillinaeHaplorhiniHumansAlbendazoleAnthelminticsAuranofinDiethylcarbamazineFilaricidesIvermectin

Identifiers

PMID25700363
PMCPMC4336141
OpenAlexW1983407912

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.