Novel drug targets for treatment of cryptosporidiosis.


Journal

Expert opinion on therapeutic targets
ISSN: 1744-7631
Titre abrégé: Expert Opin Ther Targets
Pays: England
ID NLM: 101127833

Informations de publication

Date de publication:
09 2020
Historique:
pubmed: 20 6 2020
medline: 10 4 2021
entrez: 20 6 2020
Statut: ppublish

Résumé

Introduction Cryptosporidium species are protozoan parasites that are important causes of diarrheal disease including waterborne outbreaks, childhood diarrhea in resource-poor countries, and diarrhea in compromised hosts worldwide. Recent studies highlight the importance of cryptosporidiosis in childhood diarrhea, malnutrition, and death in resource-poor countries. Despite this, only a single drug, nitazoxanide, has demonstrated efficacy in human cryptosporidiosis and its efficacy is limited in malnourished children and patients with HIV. Areas covered In this review, we highlight work on potential targets for chemotherapy and review progress on drug development. A number of new targets have been identified for chemotherapy and progress has been made at developing drugs for these targets. Targets include parasite kinases, nucleic acid synthesis and processing, proteases, and lipid metabolism. Other groups have performed high-throughput screening to identify potential drugs. Several compounds have advanced to large animal studies. Expert opinion Development of drugs for cryptosporidiosis has been plagued by a lack of success. Barriers have included poor correlations between in vitro activity and clinical success as well as frequent unanticipated adverse effects. Without a clear pathway forward, it is wise to maintain a diverse development pipeline. Drug developers should also realize that success will likely require a sustained, methodical effort.

Identifiants

pubmed: 32552166
doi: 10.1080/14728222.2020.1785432
doi:

Substances chimiques

Antiprotozoal Agents 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

915-922

Auteurs

Beilin Wang (B)

Infectious Disease Division, Department of Internal Medicine, University of Texas Medical Branch , Galveston, TX, USA.

Alejandro Castellanos-Gonzalez (A)

Infectious Disease Division, Department of Internal Medicine, University of Texas Medical Branch , Galveston, TX, USA.

A Clinton White (AC)

Infectious Disease Division, Department of Internal Medicine, University of Texas Medical Branch , Galveston, TX, USA.

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Classifications MeSH