posted on 2012-10-24, 08:59authored byP. A. Jansen, D. Rodijk-Olthuis, Edward J. Hollox, M. Kamsteeg, G. S. Tjabringa, G. J. de Jongh, I. M. van Vlijmen-Willems, J. G. Bergboer, M. M. van Rossum, E. M. de Jong, M. den Heijer, A. W. Evers, M. Bergers, J. A. Armour, P. L. Zeeuwen, J. Schalkwijk
Previous studies have extensively documented antimicrobial and chemotactic activities of beta-defensins. Human beta-defensin-2 (hBD-2) is strongly expressed in lesional psoriatic epidermis, and recently we have shown that high beta-defensin genomic copy number is associated with psoriasis susceptibility. It is not known, however, if biologically and pathophysiologically relevant concentrations of hBD-2 protein are present in vivo, which could support an antimicrobial and proinflammatory role of beta-defensins in lesional psoriatic epidermis.