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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/21367
Title: Immunostimulatory CpG oligodeoxynucleotide confers protection in a murine model of infection with Burkholderia pseudomallei
Authors: Surasakdi Wongratanacheewin
Wannapa Kespichayawattana
Pakamas Intachote
Sathit Pichyangkul
Rasana W. Sermswan
Arthur M. Krieg
Stitaya Sirisinha
Khon Kaen University
Chulabhorn Research Institute
Armed Forces Research Institute of Medical Sciences, Thailand
Mahidol University
Pfizer Inc.
Keywords: Immunology and Microbiology;Medicine
Issue Date: 1-Aug-2004
Citation: Infection and Immunity. Vol.72, No.8 (2004), 4494-4502
Abstract: Although CpG oligodeoxynucleotides (CpG ODNs) are known to enhance resistance against infection in a number of animal models, little is known about the CpG-induced protection against acute fatal sepsis such as that associated with the highly virulent bacterium Burkholderia pseudomallei. We previously demonstrated in an in vitro study that immunostimulatory CpG ODN 1826 enhances phagocytosis of B. pseudomallei and induces nitric oxide synthase and nitric oxide production by mouse macrophages. In the present study, CpG ODN 1826 given intramuscularly to BALB/c mice 2 to 10 days prior to B. pseudomallei challenge conferred better than 90% protection. CpG ODN 1826 given 2 days before the bacterial challenge rapidly enhanced the innate immunity of these animals, judging from the elevated serum levels of interleukin-12 (IL-12)p70 and gamma interferon (IFN-γ) over the baseline values. No bacteremia was detected on day 2 in 85 to 90% of the CpG-treated animals, whereas more than 80% of the untreated animals exhibited heavy bacterial loads. Although marked elevation of IFN-γ was found consistently in the infected animals 2 days after the bacterial challenge, it was ameliorated by the CpG ODN 1826 pretreatment (P = 0.0002). Taken together, the kinetics of bacteremia and cytokine profiles presented are compatible with the possibility that protection by CpG ODN 1826 against acute fatal septicemic melioidosis in this animal model is associated with a reduction of bacterial load and interference with the potential detrimental effect of the robust production of proinflammatory cytokines associated with B. pseudomallei multiplication.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=3342894608&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/21367
ISSN: 00199567
Appears in Collections:Scopus 2001-2005

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