All Journals > The Journal of Infectious Diseases > 15 January 2007 > US Capitol Bioterrorism Anthrax Exposure

Article Tools

Search for Related Articles

  • By Author
  • Search In

Announcements

Science Watch logo

JID Article Named "New Hot Paper" by ScienceWatch.com

Dr. Lauri Hicks' 2007 article on pneumococcal disease has been named a "hot new paper" by Thompson Reuters' ScienceWatch.com. Read a Q&A about the article with Dr. Hicks here

Press Release

Unique Collaboration Charts the Migrations of a Parasite that Affected History
Researchers Sequence Louse DNA from Mummies and Propose New Model for its Development


In the News

Featured in Grist
"Another symptom of swine flu: instant amnesia" May 11, 2009
Swine Influenza Virus: Zoonotic Potential and Vaccination Strategies for the Control of Avian and Swine Influenzas
Eileen Thacker and Bruce Janke
Read the veterinary literature on swine flu and you get a strong sense of what might be called vaccination treadmill: the hog industry is literally scrambling to generate new vaccines for the rapidly evolving flu strains that sweep through CAFOs. Writing in the Journal of Infectious Diseases [PDF] in 2008, Eileen Thacker and Bruce Janke of Iowa State University paint a stark picture: “A number of genetically diverse viruses are circulating in swine herds throughout the world and are a major cause of concern to the swine industry,” they write. “Influenza virus infections in swine and poultry are potential sources of viruses for the next pandemic among humans.”

Featured in New York Times
"Fear of a Swine Flu Epidemic in 1976 Offers Some Lessons, and Concerns, Today" May 8, 2009
Anti‐Ganglioside Antibody Induction by Swine (A/NJ/1976/H1N1) and Other Influenza Vaccines: Insights into Vaccine‐Associated Guillain‐Barré Syndrome
Irving Nachamkin, Sean V. Shadomy, Anthony P. Moran, Nancy Cox, Collette Fitzgerald, Huong Ung, Adrian T. Corcoran, John K. Iskander, Lawrence B. Schonberger, and Robert T. Chen
Irving Nachamkin, a professor of pathology and laboratory medicine at the University of Pennsylvania, examined some 1976 vaccine that had been saved by a scientist in Texas. In a paper published last year in The Journal of Infectious Diseases, he and colleagues reported that mice given the vaccine made antibodies that reacted with gangliosides, which are components of nerve cells. An antibody attack on gangliosides is part of the disease mechanism of Guillain-Barré.

Featured in AFP
"Swine flu vaccine 'could be ready soon'" May 7, 2009
A Broadly Protective Vaccine against Globally Dispersed Clade 1 and Clade 2 H5N1 Influenza Viruses
Mary A. Hoelscher, Neetu Singh, Sanjay Garg, Lakshmi Jayashankar, Vic Veguilla, Aseem Pandey, Yumi Matsuoka, Jacqueline M. Katz, Ruben Donis, Suresh K. Mittal, and Suryaprakash Sambhara
The vaccine Mittal created for the bird flu worked on three different strains isolated over a seven-year period and was described in papers for the Journal of Infectious Diseases and the journal Clinical Pharmacology and Therapeutics.

Featured in Newsweek
"The Path of a Pandemic" http://www.newsweek.com/id/195692
Swine Influenza Virus: Zoonotic Potential and Vaccination Strategies for the Control of Avian and Swine Influenzas
Eileen Thacker and Bruce Janke
Last year researchers from Iowa State University in Ames warned that pigs located in industrial-scale farms were being subjected to influenza infections from farm poultry, wild birds and their human handlers. Writing in The Journal of Infectious Diseases, Eileen Thacker and Bruce Janke said, "As a result of the constantly changing genetic makeup of individual influenza viruses in pigs, the U.S. swine industry is continually scrambling to respond to the influenza viruses circulating within individual production systems."

15 January 2007

Volume 195, Number 2
The Journal of Infectious Diseases 2007;195:174–184
0022-1899/2007/19502-0005$15.00
DOI: 10.1086/510312
MAJOR ARTICLE

The US Capitol Bioterrorism Anthrax Exposures: Clinical Epidemiological and Immunological Characteristics

Denise L. Doolan,1,6,a

Daniel A. Freilich,2,4,5,a

Gary T. Brice,1,b

Timothy H. Burgess,1,4,5

Mara P. Berzins,1,7

Robert L. Bull,3,7

Norma L. Graber,1,7

Jason L. Dabbs,3,7

Lori L. Shatney,1,7

David L. Blazes,4,5,b

Lolita M. Bebris,1,7

Maria F. Malone,1,7

John F. Eisold,5,8

Alfred J. Mateczun,3,5 and

Gregory J. Martin4,5,b

1Infectious Diseases Directorate, 2Combat Casualty Directorate, and 3Biological Defense Research Directorate, Naval Medical Research Center, Silver Spring, 4Infectious Diseases Service, National Naval Medical Center, and 5Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, 6Department of Molecular Microbiology and Immunology, School of Hygiene and Public Health, Johns Hopkins University, Baltimore, and 7Henry M. Jackson Foundation, Rockville, Maryland; 8Office of the Attending Physician to Congress, United States Capitol, Washington, DC

Background.Bioterrorism‐related anthrax exposures occurred at the US Capitol in 2001. Exposed individuals received antibiotics and anthrax vaccine adsorbed immunization.

Methods.A prospective longitudinal study of 124 subjects—stratified on the basis of spore exposure, nasopharyngeal culture results, and immunization status from inside and outside an epidemiologically defined exposure zone—was performed to describe clinical outcome and immune responses after Bacillus anthracis exposure. Antibody and cell‐mediated immune (CMI) responses to protective antigen (PA) and lethal factor were assayed by enzyme‐linked immunosorbent assay and fluorescence‐activated cell sorting.

Results.Antibody and CMI dose‐exposure responses, albeit generally of low magnitude, were seen for unimmunized subjects from inside, within the perimeter, and outside the exposure zone and in nonexposed control subjects. Anti‐PA antibody and CMI responses were detected in 94% and 86% of immunized subjects. No associations were seen between symptoms and exposure levels or immune responses.

Conclusions.Anthrax spores primed cellular and possibly antibody immune responses in a dose‐dependent manner and may have enhanced vaccine boost and recall responses. Immune responses were detected inside the perimeter and outside the exposure zone, which implies more‐extensive spore exposure than was predicted. Despite postexposure prophylaxis with antibiotics, inhalation of B. anthracis spores resulted in stimulation of the immune system and possibly subclinical infection, and the greater the exposure, the more complete the immune response. The significance of low‐level exposure should not be underestimated.

Received 13 March 2006; accepted 27 June 2006; electronically published 6 December 2006.

  • (See the editorial commentary by Hadler, on pages 163–4.)

Reprints or correspondence: Dr. Denise Doolan, Infectious Diseases Directorate, Naval Medical Research Center, Silver Spring, MD 20910‐7500 ().

Cited by

M. A. K. Ryan, T. C. Smith, C. J. Sevick, W. K. Honner, R. A. Loach, C. A. Moore, J. D. Erickson. (2008) Birth Defects among Infants Born to Women Who Received Anthrax Vaccine in Pregnancy. American Journal of Epidemiology 168:4, 434-442
Online publication date: 30-Jul-2008.
CrossRef
Margaret E. Coleman, Brandolyn Thran, Stephen S. Morse, Martin Hugh-Jones, Stacey Massulik. (2008) Inhalation Anthrax: Dose Response and Risk Analysis. Biosecurity and Bioterrorism: Biodefense Strategy, Practice, and Science 6:2, 147-160
Online publication date: 1-Jul-2008.
CrossRef
Prasith Baccam, Michael Boechler. (2007) Public Health Response to An Anthrax Attack: An Evaluation of Vaccination Policy Options. Biosecurity and Bioterrorism: Biodefense Strategy, Practice, and Science 5:1, 26-34
Online publication date: 1-Apr-2007.
CrossRef
James L. Hadler. (2007) Learning from the 2001 Anthrax Attacks: Immunological Characteristics. The Journal of Infectious Diseases 195:2, 163-164
Online publication date: 15-Jan-2007.
  • Presented in part: 40th Annual Meeting of the Infectious Disease Society of America, Chicago, 27 October 2002 (late breaker abstract, oral presentation); American Society of Tropical Medicine and Hygiene, Denver, 11 November 2002 (late breaker abstract, oral presentation).

    Potential conflicts of interest: none reported.

    Financial support: US Army Medical Research Material Command (funds allocated to the Naval Medical Research and Development Center, work units N3239802RCCDD001 B998 and 61102A.S13.F.A0009). The funding source had no impact on design, conduct, and reporting of the study.

    The views expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the Department of the Navy, the Department of Defense. nor the US Government.

  • D.L.D. and D.A.F. contributed equally to the study.

  • Present affiliations: Naval Medical Research Center Unit 2, Jakarta, Indonesia (G.T.B.); Naval Medical Research Center Detachment, Lima, Peru (D.L.B. and G.J.M.).

Close Popup