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Clinical and Diagnostic Laboratory Immunology, July 2004, p. 686-690, Vol. 11, No. 4
1071-412X/04/$08.00+0     DOI: 10.1128/CDLI.11.4.686-690.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Bifidobacterial Species Differentially Affect Expression of Cell Surface Markers and Cytokines of Dendritic Cells Harvested from Cord Blood

Sarah L. Young,1 Mary A. Simon,1 Margaret A. Baird,1 Gerald W. Tannock,1* Rodrigo Bibiloni,1 Kate Spencely,2 Juliette M. Lane,3 Penny Fitzharris,3 Julian Crane,3 Ian Town,4 Emmanuel Addo-Yobo,5 Clare S. Murray,6 and Ashley Woodcock6

Department of Microbiology and Immunology,1 Wellington Asthma Research Group, Wellington School of Medicine and Health Sciences,3 Canterbury Respiratory Research Group, Christchurch School of Medicine and Health Sciences, University of Otago,4 Queen Mary Hospital, Dunedin, New Zealand,2 Komfo Anokye Teaching Hospital, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana,5 Northwestern Respiratory Diseases Research Unit, Manchester, United Kingdom6

Received 9 February 2004/ Returned for modification 6 April 2004/ Accepted 27 April 2004

The gut microbiota may be important in the postnatal development of the immune system and hence may influence the prevalence of atopic diseases. Bifidobacteria are the most numerous bacteria in the guts of infants, and the presence or absence of certain species could be important in determining the geographic incidence of atopic diseases. We compared the fecal populations of bifidobacteria from children aged 25 to 35 days in Ghana (which has a low prevalence of atopy), New Zealand, and the United Kingdom (high-prevalence countries). Natal origin influenced the detection of bifidobacterial species in that fecal samples from Ghana almost all contained Bifidobacterium infantis whereas those of the other children did not. Choosing species on the basis of our bacteriological results, we tested bifidobacterial preparations for their effects on cell surface markers and cytokine production by dendritic cells harvested from cord blood. Species-specific effects on the expression of the dendritic-cell activation marker CD83 and the production of interleukin-10 (IL-10) were observed. Whereas CD83 expression was increased and IL-10 production was induced by Bifidobacterium bifidum, Bifidobacterium longum, and Bifidobacterium pseudocatenulatum, B. infantis failed to produce these effects. We concluded that B. infantis does not trigger the activation of dendritic cells to the degree necessary to initiate an immune response but that B. bifidum, B. longum, and B. pseudocatenulatum induce a Th2-driven immune response. A hypothesis is presented to link our observations to the prevalence of atopic diseases in different countries.

* Corresponding author. Mailing address: Department of Microbiology, University of Otago, P.O. Box 56, Dunedin, New Zealand. Phone: 64 3 479 7713. Fax: 64 3 479 8540. E-mail: gerald.tannock{at}stonebow.otago.ac.nz.

Clinical and Diagnostic Laboratory Immunology, July 2004, p. 686-690, Vol. 11, No. 4
1071-412X/04/$08.00+0     DOI: 10.1128/CDLI.11.4.686-690.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Tannock, G. W (2005). Commentary: Remembrance of microbes past. Int J Epidemiol 34: 13-15 [Full Text]  


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