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NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES

STATEMENT OF DR. ANTHONY 8. FAUCI, DIRECTOR AND ASSOCIATE

DIRECTOR FOR HIV RESEARCH

SUMMARY STATEMENT

Senator HARKIN. Now, we turn to the National Institute of Allergy and Infectious Diseases. Dr. Fauci, we have your budget request for $976.7 million, which is about 7.7 percent more than last year. I noticed that $459.3 million, or 47 percent, of your request is devoted to AIDS.

Again, we welcome you back and thank you again for your leadership of your Institute. And we would be delighted to hear your statement at this time.

Dr. Fauci. Thank you very much, Mr. Chairman.

The National Institute of Allergy and Infectious Diseases is responsible for the conduct and support of basic and clinical research on infectious diseases, many of which cause extraordinary morbidity and mortality throughout the world. One of these, as you mentioned, is the human immunodeficiency virus which causes AIDS.

In addition, we conduct and support research on the immune system which is the defense system of the body against the emergence of infections and certain neoplasms. I have come before this committee several times to discuss the research advances in these areas, and they have been truly extraordinary. However, these advances in biomedical technology have created a dilemma with their own new challenges. The public's expectation of what biomedical research can do to alleviate suffering and death caused by human diseases now clearly surpasses our available resources not only in research, but in health care delivery.

One way to bridge this gap is to prevent certain diseases before they occur, and this is particularly feasible with infectious diseases. Historically, vaccines have resulted in the saving of millions of lives and immeasurable financial costs. In this regard, the recent advances in technology have positioned us quite well to develop new vaccines for infections for which we thus far have no vaccines and more effective and safer vaccines for infections for which we already have existing vaccines.

In this regard, this past year basic and clinical research conducted by the NIAID in collaboration with the National Institute of Child Health and Human Development has resulted in the licensing of two new vaccines to protect infants against Haemophilus influenzae type b, the leading cause of bacterial meningitis in young children. This is an important advance, but just a start in NIAID's commitment to perform the basic and clinical research necessary to implement the children's vaccine initiative. The aim of this initiative is to develop an oral vaccine that provides lifelong immunity to the major diseases of childhood throughout the world. On another note, there has been a disturbing rise in morbidity and mortality due to asthma among inner city children, most of whom are minorities. NIAID recently announced eight awards to establish a network of centers to study this problem. I can tell you more about this later on.

History in general and AIDS in particular has taught us that new and emerging microbes are a constant threat to our survival. NIAID is committed to remain at the forefront of research to strengthen our basic science alert system against this ever-present threat.

PREPARED STATEMENT

In the area of gene therapy, which you have just heard about from some of my colleagues, NÍAID intramural scientists have recently demonstrated that a factor secreted by cells called gamma interferon could dramatically restore the genetically determined defective capacity of white blood cells of individuals with chronic granulomatous disease to kill potentially lethal bacteria. This is an important breakthrough in our ability to modify cellular gene function as opposed to replacing absent or defective genes, a manipulation which is akin to gene therapy.

Finally, time does not permit in this opening statement to give a summary of our AIDS activities, but I look forward to discussing this with you in our question period.

Thank you, Mr. Chairman. [The statement follows:)

STATEMENT OF DR. ANTHONY S. FAUCI

Over the past four decades, the research mission of the National Institute

of Allergy and Infectious Diseases (NIAID) has evolved to encompass illnesses

ranging from allergies to AIDS, from the common cold to exotic diseases that

devastate populations throughout the world.

These diverse areas of research

are all solidly grounded in the foundation of our Institute, which is basic

research on microbes that infect people and on the immune system that protects

us against these invaders.

This common theme underlies all of our efforts.

Today, even as biomedical researchers break new ground in immunology,

usher in the era of gene therapy, and design drugs that are highly specific

and effective against a wide range of infectious agents, such achievements

create a new challenge.

The public's expectations of what biomedical research

can do to alleviate suffering and death caused by human diseases far surpasses

our available resources.

How then can NIAID best employ its sophisticated technologies to fulfill

its mission of improving public health?

The most effective way to narrow the

growing gap between expectations and available resources is to prevent

diseases before they occur.

In the area of infectious diseases, this is best

achieved through vaccines.

Our foundation of basic research and our accomplishments in vaccine

development make NIAID uniquely positioned to lead the renaissance in

vaccinology that is being realized in the decade of the 1990s.

Historically.

vaccines have dramatically decreased or even completely eliminated infectious

diseases that have taken heavy tolls on past civilizations.

A classic example

is the complete eradication of the scourge of smallpox from the world.

Nonetheless, we have realized only a fraction of the full potential of

vaccines to prevent a wide array of infections that cause considerable

morbidity and mortality throughout the world.

Over the past several years,

natural products and synthetic peptides of organisms and, most recently.

recombinant DNA products have largely replaced whole killed or attenuated

organisms that have traditionally been used to make vaccines.

These newer

approaches have resulted in more specific and potentially less toxic vaccines.

Something more theoretical, but with considerable potential, is the

concept of intracellular immunization, which employs a form of gene therapy to

"immunize" cells against viral infection.

It involves inserting into an

individual's blood cells a gene encoding for a protein that inhibits the

growth of the target virus.

This past year, several NIAID-supported

researchers identified mutant genes of the AIDS virus that are promising

candidates for such a strategy.

Vaccines benefit people of all ages, but their impact on the health of

children is particularly important.

Many of you may be aware of a new concept

known as the "Children's Vaccine Initiative."

First proposed by the executive

director of the United Nations Children's Emergency Fund, its goal is lofty:

immunize children worldwide with an oral vaccine that provides lifelong

immunity to the major infectious diseases of childhood.

NIAID is committed to

focusing our basic research activities on surmounting the technical obstacles

inherent in creating such a vaccine.

In fact, I am pleased to be able to tell you about an important advance in

the technology for producing childhood vaccines.

In 1990, the FDA licensed

two new vaccines to protect infants against Haemophilus influenzae type B

(Hib), the leading cause of bacterial meningitis in young children.

Each

year, more than 700 children die of Hib meningitis, and several thousand

suffer long-term neurologic consequences of the disease, including mental

retardation and hearing loss.

The new vaccines now make it possible to

prevent Hib disease in children at highest risk for developing severe disease,

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The Hib vaccines use a new technology with far-reaching implications for

protecting young infants against other serious bacterial infections.

Because

of the immaturity of their immune systems, very young children do not respond

to vaccines made from the outer polysaccharide coats of some bacteria.

NIAID.,

supported extramural investigators and other scientists at the National

Institute of Child Health and Human Development overcame this problem by

pairing the Hib polysaccharide with a protein that children can respond to at

birth.

Use of the Hib conjugate vaccines will save an estimated $359 million

for every annual cohort of children that is vaccinated.

This compares with

the $17.4 million NIAID spent on research leading to the development of these

vaccines.

We are continuing our search for an improved pertussis (whooping cough)

vaccine, focusing on highly purified acellular vaccines containing only part

of the disease causing bacterium.

An NIAID-sponsored multicenter clinical

trial involving more than 2,000 children is now underway to compare

simultaneously a number of acellular pertussis vaccines with 2 conventional

whole-cell vaccines.

The data generated from this study will be used to

select vaccine candidates for a larger efficacy trial that will begin before

the end of 1991.

Effective control of other, non-infectious diseases continues to be 3 zoal

of NIAID's basic and clinical research endeavors.

Asthma is one of these

diseases and, as I mentioned last year, it is affecting a disproportionate

number of inner-city minority children.

Reports published this past fall

confirmed that despite advances in treatment, the numbers of children who are

suffering and dying from asthma are climbing in the United States.

NIAID

recently announced eight awards to establish a network of centers

to stud;

asthma in inner-city children.

The goal of the program is to identify the

factors contributing to this problem and to develop interventions to help

reverse this trend.

We are finding increasing evidence that viruses may directly or indirectly

contribute to the pathogenesis of a broad range of diseases whose etiologies

are unknown.

Last year, a newly discovered human retrovirus was linked to

Sjogren's syndrome, an uncommon autoimmune disease characterized by dryness of

the mouth and eyes.

Recent preliminary evidence from studies of heart

transplants indicates that a virus may accelerate the development of

atherosclerosis.

It appears likely that in the future viruses will be shown

to play a role in at least some connective tissue disorders and degenerative

neurological diseases, as well as cancers.

Fundamental studies in immunology have led to major advances in organ

transplantation.

In the decade of 1990s, organ and bone marrow

transplantation have entered the mainstream of clinical practice.

Last year 1

told you that NIAID grantees had developed a new hybrid molecule linking

diphtheria toxin to interleukin 2, one of several powerful chemicals known as

cytokines that are produced by the immune system.

This molecule binds to

cells that cause transplant rejection and the toxin kills the cells.

In other

studies, a monoclonal antibody was used to eliminate the cells responsible for

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