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Reading Room Production, p.380 · reading_room:exh:00093
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I realize I'm limited in to what I can share here because of the classified nature of the briefing,
but in short the briefing we received can be summed up by saying "We don't know much about
anyone wanting to use this information for malevolent reasons, so it's probably not a risk." I
would agree that few persons in the terrorism and intelligence worlds see this as a primary or
even secondary weapon of choice for international terrorism for all the obvious reasons. But the
absence of any discussions regarding international or national rogue scientists or irresponsible
researchers not using adequate biosafety to conduct "now enabled work" was a major flaw in the
briefing. These types of scientists are exactly the ones who would benefit immensely in
conducting work of serious concern with the recipe and methods defined in fully published
manuscripts. There was no discussion of eco-terrorists whose single purpose is to disrupt animal
production activities. A release of a mammalian-transmitted H5N1 virus in swine would
devastate that industry even if limited illness occurred because of the public relations issue of
"killer bird flu virus in pigs." I can't think of a worse scenario than having H5N1 virus
circulating widely in swine with a critical reassortment likely to occur and human transmission
not far off.
The briefing (or the meeting as a whole) did not cover the historical perspective of why influenza
virus is truly different than any Class A pathogen we worry about because of it the consequences
of its accidental release and our inability to stop transmission once it occurs in the community.
As bad as an accidental release of variola virus, Bacillus anthracis, Yersinia pestis, or SARS
virus might be, we could--based on agent transmissibility, incubation period, clinical
recognition and countermeasures--effectively stop a global pandemic from occurring. We can't
do that with influenza virus. There is no margin for error. We need look no further than the
reemergence of H1N1 in 1977, after a 20-year absence from global circulation. Our group has
been actively investigating the return of H1N1 in 1977, and based on that work we are convinced
it leaked out of a Russian lab that was working on a live-attenuated H1N1 virus vaccine. Again,
none of this information was addressed in the risk assessment overview.
I am particularly concerned about this aspect of the two days of deliberations, because I heard
several members remark how the security briefing had a substantial impact on their decision of
how to vote.
The use of the mutation data to enhance countermeasure preparedness.
Although this issue came up several times in terms of the importance for sharing the mutation
data for the development of countermeasures (vaccines and antiviral drugs), there were no datarelated presentations addressing this issue. Again the Science and Nature news stories of the
previous three months did an outstanding job of researching the claim that the mutation data
were critical in developing and deploying H5N1 countermeasures. The authors of the articles
interviewed a number of global experts in the area of influenza countermeasures; they concluded
there was no immediate benefit to countermeasure development or production as a result of the
availability of the mutation data. At no time was this information presented to the Board by a
disinterested expert.