JHU PH 2002-19 (JAMA: hemorrhagic fever as bioweapon)
Dennis O'Shea
dro@jhu.edu
Mon, 06 May 2002 14:23:01 -0400
JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH
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May 6, 2002
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HEMORRHAGIC FEVER VIRUSES EXAMINED AS POTENTIAL BIOWEAPONS
Ebola, Marburg, Lassa, and other viruses that cause deadly hemorrhagic
fever illnesses could be used as biological weapons, according to a report
from the Working Group on Civilian Biodefense, a panel of 26 experts
convened by the Center for Civilian Biodefense Strategies at the Johns
Hopkins Bloomberg School of Public Health. The group's consensus statement,
which appears in the May 8, 2002, issue of the Journal of the American
Medical Association (JAMA), is based on an analysis of published research
and offers public health and medical guidelines for managing a potential
attack.
Like smallpox and anthrax, the Centers for Disease Control and Prevention
(CDC) considers hemorrhagic fever viruses "category A" biological weapons
agents, because they have the potential to cause widespread illness and
death, and would require special public health preparedness measures to
contain an outbreak. The Working Group's report focuses on eight viruses:
Ebola, Marburg, Lassa fever, New World Arenavirus, Rift Valley Fever,
yellow fever, Ornsk hemorrhagic fever, and Kyasanur Forest Disease. Ebola
and Marburg, which belong to the Filoviridae family of viruses, can be
spread from person to person and are among the most deadly hemorrhagic
fever illnesses. Ebola kills 50 to 90 percent of those infected, while
Marburg is fatal 23 to 70 percent of the time.
"An outbreak of Ebola and Marburg would have a significant impact on our
society, because they carry significant morbidity and mortality, and other
than supportive medical care, there are no specific treatments," explains
lead author Luciana Borio, MD, fellow at the Johns Hopkins Center for
Civilian Biodefense Strategies and the Critical Care Medicine Department of
the National Institutes of Health. "It is not possible to predict whether
any of the hemorrhagic fever viruses are likely to be used as a bioweapon.
However, we know that it is not impossible to weaponize these viruses and
we, in medicine and public health, are obliged to prepare."
If an attack were to occur in the United States, the report notes that
diagnosing hemorrhagic fever viruses may be difficult, since most
clinicians are unfamiliar with these diseases. Most hemorrhagic fever
illnesses begin with a fever and rash, which is similar to other more
common illnesses. In addition, there are no widely available diagnostic
tests. Currently, the CDC in Atlanta, Georgia, and USAMRIID in Frederick,
Maryland, house the only facilities in the U.S. equipped to diagnose
hemorrhagic fever viruses.
According to the Working Group, few effective therapies or vaccines are
available to deal with hemorrhagic fever viruses. The antiviral drug
ribavirin is recommended only for the treatment of the Arenaviridae and the
Bunyaviridae families of viruses. For the Filoviridae (Ebola, Marburg) and
the Flaviviridae, the researchers recommend providing supportive care to
treat the symptoms of infected patients. There is a vaccine to prevent
yellow fever, but it is not widely available and it would not be useful to
provide protection after exposure.
The Working Group says strict infection controls must be used to prevent
the spread of hemorrhagic fever viruses during an outbreak, many of which
can be spread from person-to-person contact, and less commonly, via the
airborne route. The report recommends clinicians wear special protective
gear and that patients be isolated.
"The Working Group's consensus recommends improvements to our diagnostic
capacity and the development of a rapid test for diagnosing hemorrhagic
fever viruses. Research efforts should also focus on new antiviral
medications, vaccines, and a more fundamental scientific study of the
viruses that cause hemorrhagic fever illness," adds Dr. Borio.
###
"Hemorrhagic Fever Viruses as Biological Weapons, Medical and Public Health
Management" was written by Luciana Borio, MD; Thomas V. Inglesby, MD; C.J.
Peters, MD; Alan L. Schmaljohn, PhD; James M. Hughes, MD; Peter B.
Jahrling, PhD; Thomas Ksiazek, DVM, PhD; Karl M. Johnson, MD; Andrea
Meyerhoff, MD; Tara O'Toole, MD, MPH; Michael S. Ascher, MD; John Bartlett,
MD; Joel G. Breman, MD, DTPH; Edward M. Eitzen, Jr., MD, MPH; Margaret
Hamburg, MD; Jerry Hauer, MPH; D.A. Henderson, MD, MPH; Richard T. Johnson,
MD, Gigi Kwik, PhD; Marci Layton, MD; Scott Lillibridge, MD; Gary J. Nabel,
MD, PhD; Michael T. Osterholm, PhD, MPH; Trish M. Perl, MD, MSc; Philip
Russell, MD; and Kevin Tonat, DrPH, MPH and appears in the May 8 edition of
JAMA.
The participant's institution or agency provided funding for the study.
News releases from the Johns Hopkins Bloomberg School of Public Health may
be found at <http://www.jhsph.edu>. Information on the Johns Hopkins Center
for Civilian Biodefense Studies may be found at
<http://www.hopkins-biodefense.org>.
.