Why chronic wounds will not heal: a novel hypothesis

TY - JOUR

T1 - Why chronic wounds will not heal: a novel hypothesis

AU - Bjarnsholt, Thomas

AU - Kirketerp-Møller, Klaus

AU - Jensen, Peter Østrup

AU - Madsen, Kit G

AU - Phipps, Richard Kerry

AU - Krogfelt, Karen

AU - Høiby, Niels

AU - Givskov, Michael

N1 - Keywords: Bacterial Infections; Bacterial Physiological Phenomena; Biofilms; Chronic Disease; Diabetic Foot; Humans; Pressure Ulcer; Pseudomonas Infections; Pseudomonas aeruginosa; Varicose Ulcer; Wound Healing; Wounds and Injuries

PY - 2008

Y1 - 2008

N2 - The present paper presents a hypothesis aimed at explaining why venous leg ulcers, pressure ulcers, and diabetic foot ulcers develop into a chronic state. We propose that the lack of proper wound healing is at least in part caused by inefficient eradication of infecting, opportunistic pathogens, a situation reminiscent of chronic Pseudomonas aeruginosa infections found in patients suffering from cystic fibrosis (CF). We have analyzed sections from chronic wounds by fluorescence in situ hybridization and found distinct microcolonies--the basal structures of bacterial biofilms. Several researchers have previously reported that another important hallmark of biofilm formation is development of increased tolerance to various antimicrobial measures and treatments. Furthermore, the immune response to infecting bacteria in the cystic fibrosis lung is dominated by polymorphonuclear neutrophils (PMNs), and we have recently shown that in vitro biofilms of P. aeruginosa produce a shielding mechanism that offers protection from the phagocytic activity of PMNs. We hypothesize that the presence of P. aeruginosa in biofilms, and the lack of concomitant elimination by attended PMNs, are the main causes of inefficient eradication by antibiotic treatment and antimicrobial activity of the innate immune system, respectively.

AB - The present paper presents a hypothesis aimed at explaining why venous leg ulcers, pressure ulcers, and diabetic foot ulcers develop into a chronic state. We propose that the lack of proper wound healing is at least in part caused by inefficient eradication of infecting, opportunistic pathogens, a situation reminiscent of chronic Pseudomonas aeruginosa infections found in patients suffering from cystic fibrosis (CF). We have analyzed sections from chronic wounds by fluorescence in situ hybridization and found distinct microcolonies--the basal structures of bacterial biofilms. Several researchers have previously reported that another important hallmark of biofilm formation is development of increased tolerance to various antimicrobial measures and treatments. Furthermore, the immune response to infecting bacteria in the cystic fibrosis lung is dominated by polymorphonuclear neutrophils (PMNs), and we have recently shown that in vitro biofilms of P. aeruginosa produce a shielding mechanism that offers protection from the phagocytic activity of PMNs. We hypothesize that the presence of P. aeruginosa in biofilms, and the lack of concomitant elimination by attended PMNs, are the main causes of inefficient eradication by antibiotic treatment and antimicrobial activity of the innate immune system, respectively.

U2 - 10.1111/j.1524-475X.2007.00283.x

DO - 10.1111/j.1524-475X.2007.00283.x

M3 - Journal article

C2 - 18211573

SN - 1067-1927

VL - 16

SP - 2

EP - 10

JO - Wound Repair and Regeneration

JF - Wound Repair and Regeneration

IS - 1

ER -