Publications by authors named "S Lustigman"

Onchocerciasis is a devastating skin and eye disease that afflicts about 21 million people, most of whom live in sub-Saharan Africa. Its control with the microfilaricidal drug ivermectin is limited, thus necessitating the development of preclinical animal models to aid in the discovery of a macrofilaricide. Previously, we found that Onchocerca ochengi (the closest relative of the human O.

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Onchocerciasis and lymphatic filariasis are two neglected tropical diseases caused by filarial nematodes that utilize insect vectors for transmission to their human hosts. Current control strategies are based on annual or biannual mass drug administration (MDA) of the drugs Ivermectin or Ivermectin plus Albendazole, respectively. These drug regimens kill the first-stage larvae of filarial worms (i.

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Lymphatic filariasis and onchocerciasis are two major neglected tropical diseases that are responsible for causing severe disability in 50 million people worldwide, whilst veterinary filariasis (heartworm) is a potentially lethal parasitic infection of companion animals. There is an urgent need for safe, short-course curative (macrofilaricidal) drugs to eliminate these debilitating parasite infections. We investigated combination treatments of the novel anti- azaquinazoline small molecule, AWZ1066S, with benzimidazole drugs (albendazole or oxfendazole) in up to four different rodent filariasis infection models: CB.

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Background: Onchocerca volvulus is a filarial parasite that is a major cause of dermatitis and blindness in endemic regions primarily in sub-Saharan Africa. Widespread efforts to control the disease caused by O. volvulus infection (onchocerciasis) began in 1974 and in recent years, following successful elimination of transmission in much of the Americas, the focus of efforts in Africa has moved from control to the more challenging goal of elimination of transmission in all endemic countries.

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Article Synopsis
  • The emergence of drug resistance in anti-infectives highlights the urgent need for new broad-spectrum treatments for neglected tropical diseases (NTDs) caused by eukaryotic parasites, such as fungal infections.* -
  • Researchers modified the well-known antifungal drug fluconazole with organometallic groups, resulting in new compounds that not only enhance the drug's effectiveness but also broaden its application against various pathogens.* -
  • These new compounds demonstrated strong effectiveness against pathogenic fungal infections and parasitic worms, with mechanisms of action that differ from the original drug, making them promising candidates in the fight against drug-resistant infections and efforts to eliminate NTDs by 2030.*
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