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107th Congress
Session I | Session II
Testimony on Homeland Security and Bioterrorism Issues
Elias Zerhouni, M.D.
Director, National Institutes of Health
June 10, 2002
Madam Chairwoman and Members of the Subcommittee:
I am Dr. Elias Zerhouni, the Director of the National Institutes of Health. Thank you for the
opportunity to appear before you today to discuss NIH's role in biodefense and public-private research
partnerships. Dr. Anthony Fauci, Director of the National Institute of Allergy and Infectious Diseases
(NIAID), whose institute has the lead responsibility for biodefense research, also is here today and will
provide you with details on our current and future plans regarding this important area of homeland
security.
As you know, last week the President announced plans for the creation of a Department of
Homeland Security. This Department would be responsible for several distinct capabilities and
institutions that focus on specific elements of this mission. The Department would unify much of the
federal government’s efforts to develop and implement scientific and technological countermeasures to
chemical, biological, radiological, and nuclear (CBRN) terrorist threats. The Department would also
provide direction and establish priorities for national research and development, for related tests and
evaluations, and for the development and procurement of new technology and equipment to counter the
CBRN threat. The Department would incorporate and focus the intellectual energy and extensive
capacity of several important scientific institutions, including NIH and other Department of Health and
Human Services (DHHS) agencies, Lawrence Livermore National Laboratory (currently part of the
Department of Energy) and the Plum Island Animal Disease Center (Department of Agriculture).
The Department would unify our defenses against human, animal, and plant diseases that could
be used as terrorist weapons. The Department would sponsor outside research, development, and
testing to invent new vaccines, antidotes, diagnostics, and therapies against biological and chemical
warfare agents; to recognize, identify, and confirm the occurrence of an attach; and to minimize the
morbidity and mortality caused by any biological or chemical agent. We will be working with the
Administration on the development of this overall plan.
Biodefense research at NIH began long before the spate of anthrax cases that shook the Nation
last year. NIH has been working collaboratively with other Federal agencies, including the Department
of Defense and the Office of Homeland Security, and also with our non-governmental partners, in
conducting basic research and vaccine development regarding agents that potentially could be used as
weapons of bioterrorism. NIH also works closely with state and local officials as part of an overall
strategy of national biodefense. The President’s budget request for Fiscal Year 2003, which includes
$1.7 billion for NIH biodefense, will enable us to expand our ongoing activities in such areas as basic
research, comparative genomics, diagnostics, and vaccine and therapeutics development. It also
includes funds for the construction of additional biosafety laboratories to ensure that all Americans -
especially our local neighbors - will not be exposed to unnecessary risks resulting from biodefense
research. Dr. Fauci will elaborate on NIH's biodefense research portfolio.
As you requested, I am also here to testify about NIH's’s collaborations with the private sector.
These collaborations are particularly important today, for we stand on the threshold of the most exciting
and promising era of biomedical research in history. Over the next decade, we can expect to see
exponential growth in our understanding of human disease and ways of minimizing, and in some cases
eliminating, human suffering from a variety of vexing diseases. Collaboration has never been more
important to our success. Progress will depend on being able to assemble multidisciplinary teams of scientists, cross-cutting initiatives, and public-private
partnerships. NIH is actively pursuing research partnerships and collaborations across the world. And some of our
most valuable partners are and will be right here in Montgomery County.
I want you to know about one example of these partnerships,
which happens to involve biodefense research. On May 9, 2002,
the NIAID announced the results of research that completed
the genetic comparison of two important isolates of the anthrax
bacterium: the well-known Ames strain and an isolate from
the recent Florida anthrax attacks. The study was conducted
by scientists at the Institute for Genomic Research (TIGR),
based in Montgomery County, as well as researchers from Northern
Arizona University. NIAID partnered with the Office of Naval
Research, the National Science Foundation, and other agencies
to fund the research. The study demonstrates how a new technology
- whole-genome sequencing - and computational methods can
successfully analyze anthrax and other bacterial outbreaks,
both naturally-occurring and planned releases. These techniques
will enable researchers to more accurately trace the origin
of individual bacterial strains, determine if those strains
have been genetically modified, and assess differences in
their ability to cause disease or resist antibiotics.
To build on this research, the NIAID has awarded additional
funding to TIGR, in collaboration with Northern Arizona University,
for an expanded, comprehensive genomic analysis of at least
14 Bacillus anthracis strains and closely related bacteria.
This success is one of the early fruits of the six-year, $25
million contract NIAID entered into last year with TIGR to
establish a functional genomics resource center. With NIAID
support, scientists from TIGR and other institutions have
already finished sequencing the DNA of many pathogens, including
those that can cause tuberculosis, cholera, chlamydial infections
and syphillis. The Pathogen Functional Genomics Resource Center
at TIGR will continue to be a valuable central training and
resource facility supporting research on pathogens.
Another local example of NIH partnerships with the private sector is the $58
million in awards to sequence the genome of the rat to Celera
Genomics, located in Montgomery County, and Baylor School
of Medicine, made jointly by the National Human Genome Research
Institute (NHGRI), and the National Heart, Lung, and Blood
Institute (NHLBI) in 2001.
The rat genome sequence will further accelerate genomic-based research leading
to improved understanding of how human genes work. The scientists
involved in this project are using a strategy that combines
elements of a hierarchical shotgun, or map-based approach,
and a whole-genome-shotgun approach.
Data from the project will be released weekly into public databases at the National Center for
Biotechnology Information. Scientists from TIGR are also collaborating in this effort.
Partnerships between NIH and the private sector often involve transfers of technologies from
our intramural research laboratories to commercial companies for further research and development.
Such transfers involve the creation of new therapeutic drugs and vaccines, diagnostics, and research
resources to assist the research enterprise in developing new products to improve public health. The
NIH is one of the premier biotechnology transfer operations in the world and generates approximately
70 percent of the royalty income from the entire Federal Government.
Of the nearly 1,500 currently active licenses the NIH administers, 77 are with firms in
Montgomery County, Maryland. These firms include the following: GenVec, Inc., AlbaPharm,
EntreMed, MedImmune, 20/20 Gene Systems, OmniViral Therapeutics, Genetic Therapy, Inc,
RegeneRx Biopharmaceuticals, Veritas, Invitrogen, BioReliance Corporation, and Intracel Corp.
Currently, technologies developed in NIH laboratories are a part of over 200 products on the
market, including 15 therapeutic drugs and vaccines. Two of those therapeutic drugs are produced and
distributed by MedImmune, Inc., a firm headquartered in Montgomery County.
One of the drugs is Synagis, a monoclonal antibody used for the prevention and treatment of
serious lower respiratory tract disease by respiratory syncytial virus (RSV). RSV is the most common
cause of pneumonia and bronchiolitis in infancy and early childhood. Synagis is the world’s first
monoclonal antibody licensed by the FDA for any infectious disease. The other drug is NeuTrexin, a
treatment used to treat infections in AIDS patients that do not respond well to standard therapy.
The NIH also has a number of public-private partnerships through the Cooperative Research
and Development Agreement (CRADA) mechanism. The purpose of a CRADA is to make
Government facilities, intellectual property, and expertise available for collaborative interactions to
further the development of scientific and technological knowledge into useful, marketable products.
Currently we have 274 active CRADA projects active at the NIH. Of those active CRADAs, 25 are
with Maryland companies, including several with components located in Montgomery County:
EntreMed, Novavax, Gene Logic, Human Genome Sciences and MedImmune, to name a few.
Partnerships and mechanisms such as those I have mentioned also will prove useful in our efforts related
to biodefense.
This concludes my statement, Madame Chairwoman. I will be pleased to answer any questions
you may have.
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