Evidence map›Paper›PMID 18978536›Full record

ReviewCurrent opinion in infectious diseases2008

Development of protease inhibitors for protozoan infections.

James H McKerrow, Philip J Rosenthal, Ryan Swenerton, Patricia Doyle

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in infectious diseases, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
10.5field-weighted citation impact, top 2% 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

48 citing papers in PubMed, 124 citations in OpenAlex.

  1. Parasitology · 2026
    Review
  2. Oral infectivity through carnivorism in murine model ofFrontiers in cellular and infection microbiology · 2024
    Article
  3. Article
  4. Article
  5. Variations in active proteases ofJournal of parasitic diseases : official organ of the Indian Society for Parasitology · 2022
    Article
  6. Review
  7. Article
  8. Mechanisms Associated withLife (Basel, Switzerland) · 2021
    Review
  9. In vitro susceptibility of humanSaudi journal of biological sciences · 2021
    Article
  10. Article
  11. Article
  12. Repurposing Carvedilol as a Novel Inhibitor of theFrontiers in cellular and infection microbiology · 2021
    Article
  13. Biomolecules · 2020
    Article
  14. Structure-Based Virtual Screening and In Vitro Evaluation of NewInternational journal of molecular sciences · 2019
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  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 at 1 institution in 1 country.

James H McKerrowDepartment of Pathology, University of California San Francisco, 1700 4th Street, San Francisco, CA 94158-2330, USA. jmck@cgl.ucsf.edu
Philip J Rosenthal
Ryan Swenerton
Patricia Doyle
University of California, San Francisco · US

Funding

X-RAY CRYSTALLOGRAPHYP01AI035707 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MCKERROW, JAMES H. · 1995 to 2008
$7.8M
NIAID NIH HHS P01 AI035707
6 · The paper itself

Abstract

purpose of reviewTo highlight the promise of parasite proteases as targets for development of new antiparasitic chemotherapy. Proteolytic enzymes play key roles in the life cycle of protozoan parasites or the pathogenesis of diseases they produce. These roles include processing of host or parasite surface proteins for invasion of host cells, digestion of host proteins for nutrition, and inactivation of host immune defense mediators. RECENT

findingsDrug development for other markets has shown that proteases are druggable targets, and protease inhibitors are now licensed or in clinical development to treat hypertension, diabetes, thrombosis, osteoporosis, infectious diseases, and cancer. Several protease targets have been validated by genetic or chemical knockout in protozoan parasites. Many other parasite proteases appear promising as targets, but require more work for validation, or to identify viable drug leads. Because homologous proteases function as key enzymes in several parasites, targeting these proteases may allow development of a single compound, or a set of similar compounds, that target multiple diseases including malaria, trypanosomiasis, leishmaniasis, toxoplasmosis, cryptosporidiosis, and amebiasis. SUMMARY: Proteases have been validated as targets in a number of parasitic infections. Proteases are druggable targets as evidenced by effective antiprotease drugs for the treatment of many human diseases including hypertension and AIDS. Future drug development targeting parasite proteases will be aided by the strong foundation of biochemical, structural, and computational databases already published or available online.

Indexed as

AnimalsAntiprotozoal AgentsEukaryotaHumansProtease InhibitorsProtozoan InfectionsAntiprotozoal AgentsProtease Inhibitors

Identifiers

PMID18978536
PMCPMC2732359
OpenAlexW1990969484

What OpenQuestion holds

Textmetadata
LicenceTDM
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.