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    Schistosomiasis

    Scientists think they are a step closer to a new drug to treat schistosomiasis. More than two hundred million people suffer from this parasitic worm disease. Most live in developing nations. About ten percent of victims become seriously disabled from internal bleeding, iron loss, organ damage or other effects.

    A team in the United States found that chemical compounds known as oxadiazoles can attack an enzyme needed for the survival of Schistosoma. This is the group of flatworms that cause schistosomiasis.

    The scientists tested oxadiazoles on laboratory mice. They found that one compound killed the parasite at every level of development. The study also showed that the compound was active against all three major kinds of Schistosoma worms that infect human beings.

    America's National Institutes of Health supported the research. Nature Medicine magazine reported on the study by scientists from Illinois State University and the Chemical Genomics Center at N.I.H.

    David Williams led the research. He says the Schistosoma parasite needs oxygen to survive. Oxygen use produces oxygen-free radicals that can destroy an organism. The worm has a protective enzyme. But Professor Williams says the experimental drug disables this enzyme, causing the worm to self-destruct.
    Each year, two hundred eighty thousand people die of schistosomiasis, also known as bilharzia or snail fever. The microscopic worms infect snails, which produce infected eggs. People become infected when they enter fresh water where the snails live.

    The worms dig through skin to enter the body. They move into blood passages that supply the intestinal and urinary systems. Then, if worm eggs in human waste enter fresh water, more snails and people become infected.

    Since the nineteen eighties, doctors have used one main drug to treat schistosomiasis. Public health experts worry that the worms will become resistant to this drug, praziquantel.

    More studies are needed on the experimental drug. The scientists say the results in mice were better than all the targets set by the World Health Organization for new schistosomiasis compounds. They hope the drug will be ready for testing in humans in four to five years.

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