Abstract |
The Gram-negative bacterium Burkholderia pseudomallei is the causative agent of melioidosis, a major cause of lethal sepsis and morbidity in endemic areas of Southeast Asia and a potential bioterrorism threat. We have used susceptible BALB/c mice to evaluate the potential of targeting vaccination and generic immunotherapy to the lung for optimal protection against respiratory challenge. Intranasal vaccination with live attenuated B. pseudomallei increased survival and induced interferon-γ-secreting T cells in the lung. Intranasal delivery of CpG oligodeoxynucleotides also provided significant protection; however, combining preexposure vaccination with CpG treatment at the time of infection or up to 18 hours after infection, provided significantly greater protection than either treatment alone. This combination prolonged survival, decreased bacterial loads by >1000-fold, and delayed the onset of sepsis. This novel approach may be applicable to other potential biodefense agents for which existing countermeasures are not fully effective.
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Authors | Anna Easton, Ashraful Haque, Karen Chu, Natasha Patel, Roman A Lukaszewski, Arthur M Krieg, Richard W Titball, Gregory J Bancroft |
Journal | The Journal of infectious diseases
(J Infect Dis)
Vol. 204
Issue 4
Pg. 636-44
(Aug 15 2011)
ISSN: 1537-6613 [Electronic] United States |
PMID | 21791666
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Adjuvants, Immunologic
- Bacterial Vaccines
- Biological Warfare Agents
- CPG 10101
- CpG ODN 2395
- Oligodeoxyribonucleotides
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Topics |
- Adjuvants, Immunologic
(pharmacology)
- Animals
- Bacterial Vaccines
(immunology)
- Biological Warfare Agents
- Burkholderia pseudomallei
- CpG Islands
(immunology)
- Female
- Lung
(microbiology)
- Melioidosis
(drug therapy, microbiology, prevention & control)
- Mice
- Mice, Inbred BALB C
- Oligodeoxyribonucleotides
(immunology, pharmacology)
- T-Lymphocytes
(physiology)
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