[HTML][HTML] Critical role for CXCR2 and CXCR2 ligands during the pathogenesis of ventilator-induced lung injury

JA Belperio, MP Keane, MD Burdick… - The Journal of …, 2002 - Am Soc Clin Investig
JA Belperio, MP Keane, MD Burdick, V Londhe, YY Xue, K Li, RJ Phillips, RM Strieter
The Journal of clinical investigation, 2002Am Soc Clin Investig
Mortality related to adult respiratory distress syndrome (ARDS) ranges from 35% to 65%.
Lung-protective ventilator strategies can reduce mortality during ARDS. The protective
strategies limit tidal volumes and peak pressures while maximizing positive end-expiratory
pressure. The efficacy of this approach is due to a reduction of shear-stress of the lung and
release of inflammatory mediators. Ventilator-induced lung injury (VILI) is characterized by
inflammation. The specific mechanism (s) that recruit leukocytes during VILI have not been …
Mortality related to adult respiratory distress syndrome (ARDS) ranges from 35% to 65%. Lung-protective ventilator strategies can reduce mortality during ARDS. The protective strategies limit tidal volumes and peak pressures while maximizing positive end-expiratory pressure. The efficacy of this approach is due to a reduction of shear-stress of the lung and release of inflammatory mediators. Ventilator-induced lung injury (VILI) is characterized by inflammation. The specific mechanism(s) that recruit leukocytes during VILI have not been elucidated. Because the murine CXC chemokines KC/CXCL1 and MIP-2/CXCL2/3, via CXCR2, are potent neutrophil chemoattractants, we investigated their role in a murine model of VILI. We compared two ventilator strategies in C57BL/6 mice: high peak pressure and high stretch (high peak pressure/stretch) versus low peak pressure/stretch for 6 hours. Lung injury and neutrophil sequestration from the high–peak pressure/stretch group were greater than those from the low–peak pressure/stretch group. In addition, lung expression of KC/CXCL1 and MIP-2/CXCL2/3 paralleled lung injury and neutrophil sequestration. Moreover, in vivo inhibition of CXCR2/CXC chemokine ligand interactions led to a marked reduction in neutrophil sequestration and lung injury. These findings were confirmed using CXCR2–/– mice. Together these experiments support the notion that increased expression of KC/CXCL1 and MIP-2/CXCL2/3 and their interaction with CXCR2 are important in the pathogeneses of VILI.
The Journal of Clinical Investigation