Non-antibotic drug shows
promise in deadly C. difficile infections
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[September 24, 2015]
By Julie Steenhuysen
CHICAGO (Reuters) - A non-antibiotic drug
already tested in people for other uses may be active in treating
Clostridium difficile, a superbug that preys on people whose protective
gut bacteria have been wiped out by antibiotics.
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Studies in mice by researchers at Stanford University School of
Medicine showed that the drug ebeselen, a compound being studied in
clinical trials for a variety of other conditions, blocked
infections by disabling the bacteria's toxins. The study was
published on Wednesday in Science Translational Medicine.
C. difficile is an antibiotic-resistant infection that can cause
diarrhea, colitis, the inflammation of the colon. It infects nearly
half a million people in the United States each year and contributes
to 29,000 deaths.
Patients who get these infections are treated with antibiotics,
which wipe out friendly bacteria and contribute to antibiotic
resistance.
In the new study, led by Kristina Oresic Bender and colleagues at
Stanford, the team looked for compounds that would simply keep the
bacteria from making people sick, allowing normal, protective gut
bacteria to remain intact.
The team searched through a federal library of compounds for drugs
that targeted C. difficile’s toxins.
They settled on ebselen, an antioxidant tested in late-stage trials
by Daiichi Sankyo as a stroke treatment, but never reached the
market and is now off patent.
In studies in mice, the compound curbed infections, including those
caused by a drug-resistant strain of C. difficile, blocking both
inflammation and colon damage in treated mice.
The Stanford team hopes to move the drug rapidly into clinical
trials for treating C. difficile infection.
Dr. Alexander Khoruts, a C. difficile expert from the University of
Minnesota who was not involved in the research, said the approach of
targeting toxins instead of trying to wipe out bacteria "seems
promising" in animals.
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But Khoruts said many questions remain. He said studies in people
need to determine the most effective dose and duration of treatment,
as well as establish potential toxicity of the compound.
Several groups are working on alternatives to antibiotics for C.
difficile. Last week, Merck & Co said its experimental antibody cut
the risk that C. difficile infections would return. Others are
working on vaccines to fight the infections.
Doctors also treat patients with "stool transplants" - inserting
fecal material from a healthy person into the gut of someone with
severe diarrhea to restore friendly bacteria.
(The story was refiled to correct the spelling of C. difficile in
the headline)
(Reporting by Julie Steenhuysen; Editing by Bernard Orr)
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