(NEW ORLEANS, February 10, 1999) Autoimmune Technologies, LLC, a New Orleans biotechnology company, today
announced that scientists have discovered a new antibody in the blood of many fibromyalgia patients. This research is described
in an article entitled "Anti-Polymer Antibody Reactivity in a Subset of Patients with Fibromyalgia Correlates with Severity,"
which appears in the February 1999 issue of The Journal of Rheumatology, a prominent scientific journal.
Using a patented blood test called the Anti-Polymer Antibody Assay, or APA Assay, researchers found anti-polymer
antibodies in approximately one-half of all patients who were diagnosed with fibromyalgia and in more than 60% of the
fibromyalgia patients with severe fibromyalgia symptoms. Patients with diseases frequently confused with fibromyalgia, including
rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis/scleroderma, had a much lower incidence of these
antibodies than did the fibromyalgia patients.
Fibromyalgia syndrome is a chronic pain disorder that affects millions of individuals, primarily women, in many countries
throughout the world. The cause or causes of fibromyalgia are currently unknown, but researchers have suggested that trauma,
infection, and exposure to environmental factors may all participate in the development of this debilitating illness. Together with
widespread pain and tender points in various areas of the body, signs and symptoms include fatigue, sleep disorder, morning
stiffness, headache, cognitive problems, and other symptoms. In the United States, some 3% to 5% of adult women meet the
strict diagnostic criteria of the American College of Rheumatology for fibromyalgia, but as many as 15% to 20% of adult
women may have fibromyalgia-like symptoms.
Fibromyalgia syndrome is often difficult to diagnose, and typically a diagnosis is reached through the time-consuming and
expensive process of ruling out other illnesses that have similar symptoms. In addition, many physicians consider fibromyalgia to
be the result of aging and other normal body processes and do not regard it as a distinct clinical disorder. The resulting
reluctance on the part of some physicians to attribute their patients' symptoms to a specific illness has added considerably to the
distress of many fibromyalgia patients. Until now, there has been no laboratory test to help identify fibromyalgia.
"Our results show that there is a unique immunological response in many fibromyalgia patients," said Russell B. Wilson, Ph.D.,
president of Autoimmune Technologies and lead investigator of the published study. "We hope that these findings will lead to a
better understanding of the illness and to the development of treatments for these patients."
It is possible, Dr. Wilson pointed out, that anti-polymer antibodies are associated with one of the several different causes of
fibromyalgia, perhaps the cause that tends to produce the most severe symptoms. The published data indicate that this may be
the case, although more research will be needed. In addition to serving as a marker for fibromyalgia, he noted, it is also possible
that these antibodies are directly involved in initiating or promoting fibromyalgia.
The development of a laboratory test for fibromyalgia was welcomed by experts in the field.
"The fibromyalgia syndrome is common in clinical medicine and in the general community. We also have data on its cost," said
I. Jon Russell, M.D., Ph.D., an internationally recognized fibromyalgia investigator and clinician from the University of Texas
Health Center at San Antonio. "The direct medical costs of this disorder to the U.S. economy are over $16 billion annually. The
findings of this study raise the hopeful prospect that a new test will help us better understand fibromyalgia. Further research is
needed to confirm the clinical specificity of the test relative to other painful conditions. In addition, it will be important to
determine whether the antibody identified by this test in the blood of people with fibromyalgia is related to the cause of the
disorder or simply represents an interesting epiphenomenon," Dr. Russell said.
Associated factors appear in parallel in epiphenomena. If further research shows the production of anti-polymer antibodies to
be an epiphenomenon, the antibodies would serve as a laboratory marker for fibromyalgia without playing a direct role in the
disease process.
Kristin Thorson is president of The Fibromyalgia Network, a patient self-help organization headquartered in Tucson, Arizona,
and president of The American Fibromyalgia Syndrome Association, a charitable organization dedicated to funding research on
fibromyalgia and chronic fatigue syndrome. "In the past," Ms. Thorson said, "many health insurance companies and some
members of the medical community have argued that fibromyalgia is not real - all because no one had developed a lab marker
to indicate otherwise. Now that there is a blood marker that can be shown to correlate with disease severity, there should be
no more debate over the existence of fibromyalgia and scientists should be encouraged to research effective therapies for this
potentially disabling illness."
Robert M. Bennett, M.D., a physician and scientist who is chairman of the Division of Arthritis and Rheumatic Disease of
Oregon Health Sciences University in Portland and a widely published and internationally known expert on fibromyalgia
syndrome, said "There are two major problems for most physicians in accepting fibromyalgia. The first is the lack of an easily
performed laboratory test. The second is its recalcitrance to therapy. The promise of a potentially useful diagnostic marker is an
exciting development in this field. If the sensitivity and specificity of this test can be confirmed by independent laboratories, it
could open up an important new research avenue for a condition that compromises the quality of life of five million to ten million
U.S. women."
Autoimmune Technologies expects during 1999 to apply to the U.S. Food and Drug Administration for approval of a kit form
of the Assay as a diagnostic test. "The reproducibility of the APA Assay has already been independently demonstrated by the
National Institute of Public Health and the Environment, or RIVM, in The Netherlands," said Dr. Wilson. "The RIVM has
found the APA Assay to give reproducible results and to be useful for the evaluation of the presence of anti-polymer antibodies
in human serum. The other confirmatory studies discussed by Drs. Russell and Bennett are already well under way. These
studies, together with our research published in The Journal of Rheumatology, will be included in our application to the FDA for
approval of the Assay as an in vitro diagnostic test to aid in the diagnosis of fibromyalgia."
Other authors of the article in this month's issue of The Journal of Rheumatology include Dr. Oscar S. Gluck and Dr. John R. P.
Tesser of the Arizona Rheumatology Center in Phoenix, Dr. Janet C. Rice of Tulane University School of Public Health and
Tropical Medicine, and Dr. Alan J. Bridges of the University of Wisconsin School of Medicine in Madison.
Anti-polymer antibodies were discovered by researchers at Tulane University Medical Center, where the APA Assay was
developed. Autoimmune Technologies has licensed the APA Assay from Tulane. An APA Assay kit is not currently in
commercial distribution in the U.S., although the Assay is being performed by Autoimmune Technologies as a service to
physicians and researchers for investigational use only. A kit form of the APA Assay will be available in the near future in other
countries.
The APA Assay is covered by U.S. and European patents, and patents in other countries are pending.
For further information, visit the Autoimmune Technologies Web site at www.autoimmune.com.
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