Evidence map›Paper›PMID 8980761›Full record

ArticleAntimicrobial agents and chemotherapy1997

Evaluation of selected antiprotozoal drugs in the Babesia microti-hamster model.

S E Marley, M L Eberhard, F J Steurer, W L Ellis, P B McGreevy, T K Ruebush

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 26% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Tafenoquine: A Breakthrough Option for Babesiosis Treatment.Tropical medicine and infectious disease · 2026
    Article
  3. Article
  4. Tafenoquine for Relapsing Babesiosis: A Case Series.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2024
    Article
  5. Comparative chemical genomics inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Evaluation of the Inhibitory Effect ofJournal of tropical medicine · 2023
    Article
  10. Pomegranate (Journal of parasitology research · 2022
    Article
  11. Article
  12. Effect of methanolic extract fromVeterinary world · 2022
    Article
  13. Treatment of Human Babesiosis: Then and Now.Pathogens (Basel, Switzerland) · 2021
    Review
  14. Article
  15. Longhua Chinese medicine · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Inhibitory effects of fluoroquinolone antibiotics onInfection and drug resistance · 2018
    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

6 authors at 1 institution in 1 country.

S E MarleyDivision of Parasitic Diseases, Centers for Disease Control and prevention, Department of Health and Human Services, Atlanta, Georgia 30341, USA.
M L Eberhard
F J Steurer
W L Ellis
P B McGreevy
T K Ruebush
Centers for Disease Control and Prevention · US

Funding

MOLECULAR CELL BIOLOGY OF PARASITES AND VECTORST32AI007322 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI DAMIAN, RAYMOND T · 1988 to 1997
–
NIAID NIH HHS 5T32 AI07322
6 · The paper itself

Abstract

The presently used therapy for Babesia microti infections, a combination of quinine and clindamycin, does not always result in parasitologic cures. To identify possible alternative chemotherapeutic agents for such infections, we screened, in the hamster-B. microti system, 12 antiprotozoal drugs that have either recently been released for human use or were in experimental stages of development at the Walter Reed Army Institute of Research for the treatment of malaria and leishmaniasis. Several well-recognized antimalarial drugs, such as mefloquine, halofantrine, artesunate, and artelenic acid, exhibited little or no effect on parasitemia. Two 8-aminoquinolines, WR006026 [8-(6-diethylaminohexylamino)-6-methoxy-4-methylquinoline dihydrochloride] and WR238605 [8-[(4-amino-1-methylbutyl)amino]-2,6-dimethoxy-4-methyl-5 -(3-trifluoromethylphenoxy-7) quinoline succinate], produced clearance of patent parasitemia. Furthermore, blood from infected hamsters treated with WR238605 via an intramuscular injection failed to infect naive hamsters on subpassage, thus producing a parasitologic cure. These two compounds merit further screening in other systems and may prove useful in treating human babesiosis.

Indexed as

AminoquinolinesAnimalsAntiprotozoal AgentsBabesiosisCricetinaeDrug Evaluation, PreclinicalMesocricetusPyrrolesQuinazolines8-aminoquinolineAminoquinolinesAntiprotozoal AgentsPyrrolesQuinazolinestafenoquineWR 228275

Identifiers

PMID8980761
PMCPMC163666
OpenAlexW2153437407

What OpenQuestion holds

Textmetadata
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.