Newly developed anti-malarial drug effectively treats toxoplasmosisMarch 5th, 2008 - 5:42 pm ICT by admin
Washington, Mar 5 (ANI): Researchers at the University of Chicago Medical Center have claimed that a newly developed anti-malarial drug might be 10 times more effective than the key medicine in the current gold-standard treatment for toxoplasmosis, a disease caused by a related parasite that infects nearly one-third of all humans.
The new study shows that the drug, known as JPC-2056, is extremely effective against Toxoplasma gondii, the parasite that causes toxoplasmosis, without toxicity.
“JPC-2056 has the potential to replace the standard treatment of pyrimethamine and sulfadiazine,” said infectious disease specialist Rima McLeod, professor of ophthalmology at the University of Chicago and senior author of the study.
“The drug, taken by mouth, is easily absorbed, bioavailable, and relatively nontoxic. In tissue culture and in mice, it was rapidly effective, markedly reducing numbers of parasites within just a few days, she added.
Untreated mice injected with the parasite “appeared ill,” four days after the injection, the authors note, “with ruffled fur and hunched shoulders.” Treated mice remained well.
“Studies in tissue culture found no evidence of the parasite or the plaques they produce 52 days after four days of treatment,” said co-author Ernest Mui, a researcher in McLeod’s laboratory.
“The absence of growth indicates that this compound is ‘cidal’ and not merely ’static’ for the active form of T. gondii, the authors of the study said.
The drug inhibits the action of an enzyme, dihydrofolate reductase (DHFR), produced by the family of parasites that includes those that cause toxoplasmosis and malaria. It is structurally distinct from the human DHFR.
“The drug’s effect on the malaria and Toxoplasma enzymes is robust. It has much less effect on the human enzyme, said McLeod.
Toxoplasma infection is “probably the most common parasitic infection in the world, causing very significant disease in those who have immature immune systems or who are immune-compromised. New medications are urgently needed, McLeod said.
The standard medicines to treat the infection can cause severe side effects and many patients become hypersensitive to them. There are no medicines that can eliminate certain latent stages of the parasite’s life cycle. There is no vaccine.
This new class of medicine holds “considerable promise for significant advances in the treatment of toxoplasmosis, which damages the eye and the brain as well as malaria, which kills one million children each year, said McLeod.
The study is published in PLoS Neglected Tropical Diseases. (ANI)
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Tags: chicago medical center, co author, enzymes, infectious disease, infectious disease specialist, malaria, mice, ophthalmology, parasite, parasites, parasitic infection, plaques, pyrimethamine, rima mcleod, sulfadiazine, tissue culture, toxoplasma gondii, toxoplasma infection, toxoplasmosis, university of chicago