A National Institutes of Health (NIH) clinical study of healthy adult
volunteers who consented to be infected with the 2009 H1N1 influenza
virus under carefully controlled conditions has provided researchers
with concrete information about the minimum dose of virus needed to
produce mild-to-moderate illness. The study also gives a clearer picture
of how much time elapses between a known time of infection, the start
of viral shedding (a signal of contagiousness), the development of an
immune response, and the onset and duration of influenza symptoms. The
data obtained from this study provide a basis for more rapid,
cost-effective clinical trials to evaluate new influenza drugs or to
determine the efficacy of candidate vaccines for both seasonal and
pandemic influenza.
In the study, 46 volunteers were divided into five groups and exposed
to influenza virus in escalating doses. The virus, synthesized in the
lab under Good Manufacturing Practice conditions, was genetically
identical to the virus that caused 2009 H1N1 pandemic influenza. The
volunteers all gave informed consent and subsequently were admitted to
an isolation unit at the NIH Clinical Center in Bethesda, Md., for a
minimum of eight days following virus exposure. The volunteers' health
was closely monitored throughout their stay in the clinic and for two
months afterward. The researchers sought to determine the minimum dose
of virus needed to produce both shedding of live virus in nasal
secretions and mild or moderate flu symptoms in 60 percent or more of
dosed volunteers. When the scientists administered an influenza virus
dose of 107 TCID50 (a measure of the amount of virus required to produce
cell death in 50 percent of cultured cells inoculated with virus) to 13
volunteers, 9 (or 69 percent) shed virus and developed symptoms. Lower
dosages did not generate responses that met this threshold, thereby
establishing the minimum dose of influenza virus needed to produce
mild-to-moderate illness.
Researchers from NIH's National Institute of Allergy and Infectious Diseases (NIAID) presented the preliminary study results at the Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC) meeting in Denver in September 2013.
Researchers from NIH's National Institute of Allergy and Infectious Diseases (NIAID) presented the preliminary study results at the Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC) meeting in Denver in September 2013.
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The above story is based on materials provided by NIH/National Institute of Allergy and Infectious Diseases.
Courtesy: ScienceDaily
The above story is based on materials provided by NIH/National Institute of Allergy and Infectious Diseases.
Courtesy: ScienceDaily
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