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CIDRAP- Study: Anti-parasitic drug may help flu patients

Shiloh

Editor, Senior Moderator
Source: http://www.cidrap.umn.edu/news-perspective/2014/05/study-anti-parasitic-drug-may-help-flu-patients


Study: Anti-parasitic drug may help flu patients
Filed Under:
Influenza, General
Lisa Schnirring | Staff Writer | CIDRAP News
|
May 20, 2014


An early clinical trial of a drug commonly used to treat parasitic infections cut the length of flu symptoms by about a day in patients who didn't have severe disease, a result that appears to be on par with neuraminidase inhibitors, the gold standard for treatment.

The drug studied?nitazoxanide?has a different mechanism of action than neuraminidase inhibitors and could be useful alone or in combination with other drugs as an option for treating antiviral-resistant flu strains, according to the research team, who reported their findings today in an early online edition of Lancet Infectious Diseases.

Currently, the drug is licensed in the United States to treat Cryptosporidium and Giardia infections, and it is widely used in Latin America for treating intestinal parasitic illnesses. It can inhibit flu virus replication by blocking the maturation of viral hemagglutinin and has also been shown in cell culture studies to inhibit other respiratory viruses, including parainfluenza virus, coronaviruses, and respiratory syncytial virus.

The goal of the study was to explore the safety and efficacy of a 300-mg controlled-release tablet designed to deliver blood concentrations needed for treating viral respiratory illnesses. The study was sponsored by Romark Laboratories, the maker of the drug.

The study group included 624 patients aged 12 to 65 years who were treated at 74 primary care clinics between Dec 27, 2010, and Apr 30, 2011. Researchers recruited those who had fever, at least one respiratory symptom, and at least one other symptom of flu, such as muscle aches or chills within 48 hours of symptom onset.

The randomized trial compared the time from initiation of treatment to alleviation of symptoms for two different dosages of nitazoxanide, 300 mg or 600 mg, or placebo, all taken twice a day for 5 days. Patients were asked to record their symptoms along with any adverse events twice a day in a diary. A nurse checked in with patients on study days 2 through 5 to ask about symptoms and any complications. Patients were asked not to take antiviral drugs, but they were allowed to take acetaminophen for fever.

Patients were followed for 28 days. They returned to their respective clinics at two different times for a physical exam, blood tests, urine tests, and respiratory swabs.

The median time to alleviation of symptoms in patients with confirmed influenza was roughly 1 day (21.2 hours) shorter in those who received the larger dose of nitazoxanide than in those who received placebo, a statistically significant difference. The effect of this dosage was comparable to the benefit typical for neuraminidase inhibitor treatment, say the authors.

The 300-mg dose of nitazoxanide reduced the duration of flu symptoms by a median of 7.6 hours in comparison with placebo but this difference was not statistically significant.

Though the 600-mg nitazoxanide dosage was 20% higher and the duration 67% longer than the approved dosage for treatment of intestinal infections, the researchers found no significant change in the side-effect pattern. Also, the frequency and severity of adverse effects didn't vary significantly between any of the three groups in the study.

The researchers said limitations of the study included that the patients were enrolled during a single flu season and that the trial enrolled only60% of the intended number of participants, because of the end of the flu season. They said the next steps are to explore possible benefits in children, severely ill patients, resistant infections, and in combination with other therapies.

In a commentary that accompanied the study, two epidemiology professors from the London School of Hygiene and Tropical Medicine, Krishnan Bhaskaran, MSc, PhD, and Sara Thomas, MBBS, MSc, PhD, wrote that the group's investigation is a welcome attempt to broaden the options for fighting influenza. .

Though the study found benefit in nitazoxanide treatment for relatively healthy flu patients, current guidelines don't typically recommend any treatment in this group, and a bigger benefit could be reducing the burden of flu in vulnerable patients, the two authors wrote. "This recruitment was understandable for an early-stage placebo-controlled study, but because at present trials of high-risk individuals are only at the preparation stage, we will probably have to wait some time to understand the full public health relevance of this drug."

Among other interesting findings were no development of resistance in viral isolates from swabs taken 5 days into treatment and reduction of symptoms in patients in whom no flu virus was ultimately found, which hints at a possible broader use for the drug, the commentators wrote

Bhaskaran and Thomas wrote that a phase 3 trial is under way to look at the possible benefits of combining nitazoxanide with oseltamivir (Tamiflu).

They concluded that the early findings are promising and the drug seems worth pursuing but that the trial was small and the treatment is at an early stage of evaluation, so it's impossible to say now whether nitazoxanide will someday have a role in the fight against flu.

Haffizulla J, Hartman A, Hoppers M, et al. Effect of nitazoxanide in adults and adolescents with acute uncomplicated influenza: a double-blind, randomized, placebo-controlled, phase 2b/3 trial. Lancet Infect Dis 2014 May 19 [Abstract]

Bhaskaran K, Thomas SL. Fighting influenza?a new weapon in the armoury? (Commentary) Lancet Infect Dis 2014 May 19 [Extract]
 
Re: CIDRAP- Study: Anti-parasitic drug may help flu patients

my summary:
nitazoxanide
blocking the maturation of viral hemagglutinin

no test in mice ? useful for prophylaxis ? what ingredient

------------------------------------------
http://www.ncbi.nlm.nih.gov/pubmed/?term=nitazoxanide
Nitazoxanide for chronic hepatitis C.
----------------------------------
Analyzing the relationship of QT interval and exposure to Nitazoxanide,
a prospective candidate for influenza antiviral therapy-A formal TQT study.
--------------------------------
tropical disease
----------------------------------
Nitazoxanide inhibits the replication of Japanese encephalitis virus in cultured cells and in
a mouse model.
------------------------------------
10.Nitazoxanide: nematicidal mode of action and drug combination studies.
-----------------------------------------
Using cell culture assays, the investigational antiviral drugs nitazoxanide, favipiravir,
and fludase were shown to inhibit the replication of A(H3N2)v viruses, including the
virus with the S247P substitution in the NA.
-------------------------------------------
Addition of nitazoxanide to PEG-IFN and ribavirin to improve HCV treatment
------------------------------------------------
Current state of Clostridium difficile treatment options.
--------------------------------------------------
Nitazoxanide is a nitrothiazole derivative of salicylamide useful for the treatment
of protozoal and bacterial infections with an extended range of antiviral activity
and innovative mechanism of action, especially against hepatitis and influenza
viruses or rotaviruses.
[Niclosamide was described to be able to affect coronaviruses.]
---------------------------------------------------
[Rotavirus infections].
-------------------------------------------------
======================================================
http://en.wikipedia.org/wiki/Nitazoxanide
discovered in the 1980s
interference with the pyruvate:ferredoxin oxidoreductase (PFOR) enzyme dependent
electron transfer reaction which is essential to anaerobic energy metabolism
Following oral administration, it is rapidly hydrolyzed to its active metabolite, tizoxanide,[2]
which is 99% protein bound. Peak concentrations are observed 1–4 hours after administration.
It is excreted in the urine, bile and feces.
It has also been shown to have activity against influenza A virus in vitro.[3] The mechanism
appears to be by selectively blocking the maturation of the viral hemagglutinin at a stage
preceding resistance to endoglycosidase H digestion. This impairs hemagglutinin intracellular
trafficking and insertion of the protein into the host plasma membrane.

[i don't understand. How does HA "maturate" , HA goes into the host plasma membrane ?
what is plasma ?]

==============================================================
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2785610/
Thiazolides, a New Class of Anti-influenza Molecules Targeting Viral Hemagglutinin at the
Post-translational Level*

a key step for correct assembly and exit of the virus from the host cell.

tizoxanide pretreatment of cells up to 12 h before viral infection had no effect on flu replication.
treatment of the viral inoculum or treatment of cells only during the adsorption period did not
inhibit virus replication , indicating that the drug is not directly affecting virus infectivity,
nor its binding or entry into target cells.
TIZ treatment initiated between 0 and 3 h p.i. was the most effective in inhibiting virus replication
Treatment started at 6 h p.i. was less effective but still able to inhibit virus replication,
whereas the drug was ineffective when administered at 12 h p.i.
A single administration of the drug after virus adsorption was effective in inhibiting virus
replication for at least 48 h after infection

===============================================
Thiazolides interfere with viral hemagglutinin N-glycosylation
Tizoxanide inhibits transport of influenza hemagglutinin to the cell surface

HA maturation is influenced both by the host cell glycosylation machinery (24) and the virus strain (25).
Glycosylation of HA, like other cell surface glycoproteins, is initiated in the endoplasmic reticulum,
adding the “high mannose” oligosaccharides (26). The mannose-rich sugar component is processed
in the Golgi apparatus during the transport to the cell surface, and terminal glycosylation occurs in
trans cisternae of the Golgi apparatus (27).

25. Steinhauer D. A., Skehel J. J. (2002) Annu. Rev. Genet. 36, 305–332 [PubMed]
26. Hebert D. N., Foellmer B., Helenius A. (1995) Cell 81, 425–433 [PubMed]
27. Tatu U., Hammond C., Helenius A. (1995) EMBO J. 14, 1340–1348 [PMC free article] [PubMed]
28. Ohuchi R., Ohuchi M., Garten W., Klenk H. D. (1997) J. Virol. 71, 3719–3725 [PMC free article] [PubMed]


[i didn't know that]

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