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Neutrophil extracellular traps are pathogenic in primary graft dysfunction after lung transplantation.

Publication ,  Journal Article
Sayah, DM; Mallavia, B; Liu, F; Ortiz-Muñoz, G; Caudrillier, A; DerHovanessian, A; Ross, DJ; Lynch, JP; Saggar, R; Ardehali, A; Ware, LB ...
Published in: Am J Respir Crit Care Med
February 15, 2015

RATIONALE: Primary graft dysfunction (PGD) causes early mortality after lung transplantation and may contribute to late graft failure. No effective treatments exist. The pathogenesis of PGD is unclear, although both neutrophils and activated platelets have been implicated. We hypothesized that neutrophil extracellular traps (NETs) contribute to lung injury in PGD in a platelet-dependent manner. OBJECTIVES: To study NETs in experimental models of PGD and in lung transplant patients. METHODS: Two experimental murine PGD models were studied: hilar clamp and orthotopic lung transplantation after prolonged cold ischemia (OLT-PCI). NETs were assessed by immunofluorescence microscopy and ELISA. Platelet activation was inhibited with aspirin, and NETs were disrupted with DNaseI. NETs were also measured in bronchoalveolar lavage fluid and plasma from lung transplant patients with and without PGD. MEASUREMENTS AND MAIN RESULTS: NETs were increased after either hilar clamp or OLT-PCI compared with surgical control subjects. Activation and intrapulmonary accumulation of platelets were increased in OLT-PCI, and platelet inhibition reduced NETs and lung injury, and improved oxygenation. Disruption of NETs by intrabronchial administration of DNaseI also reduced lung injury and improved oxygenation. In bronchoalveolar lavage fluid from human lung transplant recipients, NETs were more abundant in patients with PGD. CONCLUSIONS: NETs accumulate in the lung in both experimental and clinical PGD. In experimental PGD, NET formation is platelet-dependent, and disruption of NETs with DNaseI reduces lung injury. These data are the first description of a pathogenic role for NETs in solid organ transplantation and suggest that NETs are a promising therapeutic target in PGD.

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Published In

Am J Respir Crit Care Med

DOI

EISSN

1535-4970

Publication Date

February 15, 2015

Volume

191

Issue

4

Start / End Page

455 / 463

Location

United States

Related Subject Headings

  • Respiratory System
  • Primary Graft Dysfunction
  • Platelet Activation
  • Neutrophils
  • Microscopy, Fluorescence
  • Mice, Inbred C57BL
  • Mice
  • Male
  • Lung Transplantation
  • Humans
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Sayah, D. M., Mallavia, B., Liu, F., Ortiz-Muñoz, G., Caudrillier, A., DerHovanessian, A., … Looney, M. R. (2015). Neutrophil extracellular traps are pathogenic in primary graft dysfunction after lung transplantation. Am J Respir Crit Care Med, 191(4), 455–463. https://doi.org/10.1164/rccm.201406-1086OC
Sayah, David M., Beñat Mallavia, Fengchun Liu, Guadalupe Ortiz-Muñoz, Axelle Caudrillier, Ariss DerHovanessian, David J. Ross, et al. “Neutrophil extracellular traps are pathogenic in primary graft dysfunction after lung transplantation.Am J Respir Crit Care Med 191, no. 4 (February 15, 2015): 455–63. https://doi.org/10.1164/rccm.201406-1086OC.
Sayah DM, Mallavia B, Liu F, Ortiz-Muñoz G, Caudrillier A, DerHovanessian A, et al. Neutrophil extracellular traps are pathogenic in primary graft dysfunction after lung transplantation. Am J Respir Crit Care Med. 2015 Feb 15;191(4):455–63.
Sayah, David M., et al. “Neutrophil extracellular traps are pathogenic in primary graft dysfunction after lung transplantation.Am J Respir Crit Care Med, vol. 191, no. 4, Feb. 2015, pp. 455–63. Pubmed, doi:10.1164/rccm.201406-1086OC.
Sayah DM, Mallavia B, Liu F, Ortiz-Muñoz G, Caudrillier A, DerHovanessian A, Ross DJ, Lynch JP, Saggar R, Ardehali A, Lung Transplant Outcomes Group Investigators, Ware LB, Christie JD, Belperio JA, Looney MR. Neutrophil extracellular traps are pathogenic in primary graft dysfunction after lung transplantation. Am J Respir Crit Care Med. 2015 Feb 15;191(4):455–463.

Published In

Am J Respir Crit Care Med

DOI

EISSN

1535-4970

Publication Date

February 15, 2015

Volume

191

Issue

4

Start / End Page

455 / 463

Location

United States

Related Subject Headings

  • Respiratory System
  • Primary Graft Dysfunction
  • Platelet Activation
  • Neutrophils
  • Microscopy, Fluorescence
  • Mice, Inbred C57BL
  • Mice
  • Male
  • Lung Transplantation
  • Humans