The Drugs We Have and the Drugs We Need Against Major Helminth Infections
Abstract
Parasitic worms (helminths) have accompanied humans for thousands of years and, still today, they are pervasive where poverty persists, including large parts of Southeast Asia and the Western Pacific Region. The global strategy for the control of helminth infections is morbidity control and elimination as a public health problem. Regular administration of anthelminthic drugs to at-risk populations (e.g. school-aged children) serves as the backbone of interventions in areas where helminth infections are highly endemic. In this review, we focus on soil-transmitted helminthiasis (ascariasis, hookworm disease, strongyloidiasis and trichuriasis) and food-borne trematodiasis (clonorchiasis, fascioliasis, intestinal fluke infections, opisthorchiasis and paragonimiasis) and discuss the few drugs that are currently available for their treatment and control. Emphasis is placed on efficacy with new light shed on multiple dosing and combination therapy. We summarise recent advances made with anthelminthic drugs that might become the future armentarium for the control of major helminthiasis (e.g. artemisinins, cyclooctadepsipeptides, mefloquine, monepantel, nitazoxandide, synthetic peroxides and tribendimidine). Issuing from our review are current research gaps and the need for concerted efforts to discover, develop and deploy the next generation of anthelminthic drugs.
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Mebendazole 100 mg twice daily for 3 days (total 600 mg) shows fairly higher efficacy for hookworms, with 80.0% CR and 41.0-100% ERR according to 27 trials.
“In comparison, 100 mg twice daily for 3 days (total 600 mg), the recommended dose by WHO [45], showed fairly higher efficacies of 80.0% CR and 41.0–100% ERR according to reports from 27 trials [10].”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [10]
Mebendazole 500 mg single dose shows poor efficacy for hookworms, with CR 15.0-17.6% and ERR 0-98.0%.
“Mebendazole showed poor efficacy for hookworms if used 500 mg only 1 time. Keiser and Utzinger [10] and Soukhathammavong et al. [44] reported the CRs of 500 mg single dose of mebendazole to be 15.0% and 17.6% and ERR 0–98.0% and 76.3%, respectively.”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [10]
Ascaris lumbricoides is the most highly susceptible parasite species to albendazole and mebendazole among intestinal nematodes infecting humans.
“Among various species of intestinal nematodes infecting humans, Ascaris lumbricoides is the most highly susceptible parasite species to albendazole and mebendazole [1,8–10,42–44] (Table 1).”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [10]
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References 158 · Cited by 288
- Authors
- Keiser, J., & Utzinger, J.
- Affiliations
- Swiss Tropical and Public Health Institute (CH)
- Venue
- Advances in Parasitology
- Publisher
- Elsevier
- Published
- 2010
- Volume
- 73
- Pages
- 197-230
- ISSN
- 0065-308X (ISSN-L)
- OpenAlex
- W1520664895
- Cited by
- 288
- References
- 158
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 13 · 2023: 14 · 2022: 7 · 2021: 15 · 2020: 20 · 2019: 16 · 2018: 23 · 2017: 23 · 2016: 19 · 2015: 16 · 2014: 23 · 2013: 25 · 2012: 29
- FWCI
- 32.14
- Type
- book chapter
- Language
- en
- Open access
- closed
- Locations
- Advances in Parasitology/Advances in parasitology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Topics
- Life Sciences › Immunology and Microbiology › Parasitology › Parasites and Host Interactions
- Health Sciences › Veterinary › Small Animals › Helminth infection and control
- Health Sciences › Medicine › Infectious Diseases › Parasitic Diseases Research and Treatment
- Keywords
- helminthiasis, anthelmintics, soil-transmitted helminthiasis, ascariasis, hookworm infection, strongyloidiasis, trichuriasis, trematode infection, clonorchiasis, fascioliasis, opisthorchiasis, paragonimiasis, anthelmintic efficacy, combination therapy, repeated dosing, artemisinin, mefloquine, monepantel, tribendimidine, drug development, school-aged children, morbidity control, elimination
- MeSH terms
- Animals, Anthelmintics, Asia, Southeastern, Communicable Disease Control, Drug Therapy, Combination, Helminthiasis, Helminths, Humans, Australasia, Drug Discovery
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