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Eur Respir J 2006; 27:253-260
Copyright ©ERS Journals Ltd 2006

Identification of hBD-3 in respiratory tract and serum: the increase in pneumonia

H. Ishimoto1, H. Mukae1, Y. Date2, T. Shimbara2, M. S. Mondal2, J. Ashitani2, T. Hiratsuka3, S. Kubo4, S. Kohno1 and M. Nakazato2

1 Second Dept of Internal Medicine, Nagasaki University School of Medicine, Nagasaki, 2 Third Dept of Internal Medicine, Miyazaki Medical College, University of Miyazaki, 3 National Sanatorium Miyazakihigashi Hospital, Miyazaki, and 4 Peptide Institute, Inc., Osaka, Japan.

CORRESPONDENCE: M. Nakazato, Third Dept of Internal Medicine, Miyazaki Medical College, University of Miyazaki, Kiyotake, Miyazaki 889-1692, Japan. Fax: 81 985857902. E-mail: nakazato{at}med.miyazaki-u.ac.jp

Keywords: Defensin, immunohistochemistry, pneumonia, radioimmunoassay, respiratory tract

Received: September 10, 2004
Accepted October 3, 2005

Human ß-defensin (hBD)-3, a 45 amino acid antimicrobial peptide, was originally isolated from human skin. hBD-3 mRNA has also been detected in the airways by RT-PCR. While hBD-3 may be involved in antimicrobial defences within the respiratory tract, the presence of hBD-3 peptide in the respiratory system has not yet been confirmed.

The antimicrobial activity of the synthesised hBD-3 peptide was measured by a radial diffusion assay and a colony count assay. The present authors confirmed the presence of hBD-3 peptide in homogenates of human lung and serum using reverse-phase HPLC coupled with a highly sensitive RIA. The localisation of the hBD-3 peptide was investigated by immunohistochemistry. In addition, the serum concentrations of hBD-3 were measured by RIA.

hBD-3 exhibited a strong antimicrobial activity, which was unaffected by increasing salt concentrations. Immunohistochemically, the current authors observed the expression of hBD-3 in bronchial and bronchiolar epithelial cells. The mean±SD serum concentration of hBD-3 in patients with bacterial pneumonia was 239.4±17.8 pg·mL–1 in the acute phase and, decreased to 159.3±20.1 pg·mL–1 after the completion of therapy.

In conclusion, these findings will help elucidate the role of human ß-defensin-3 in host immune responses and identify the pathophysiological significance of this molecule in respiratory infections.




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