BPI-ANCA is expressed in the airways of cystic fibrosis patients and correlates to platelet numbers and Pseudomonas aeruginosa colonization

Author:

Hovold Gisela,Lindberg Ulrika,Ljungberg Johanna K.,Shannon Oonagh,Påhlman Lisa I.

Funder

Swedish Heart and Lung foundation

Royal Physiographic Society of Lund

Swedish Heart and Lung Association

Swedish Cystic Fibrosis Association, the Alfred Österlund foundation

Magnus Bergvall foundation

Mats Kleberg foundation

MIMS Clinical Research Fellows grant

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine

Reference31 articles.

1. Origins of cystic fibrosis lung disease;Stoltz;N. Engl. J. Med.,2015

2. Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition;Kosorok;Pediatr. Pulmonol.,2001

3. A systematic review of studies examining the rate of lung function decline in patients with cystic fibrosis;Harun;Paediatr. Respir. Rev.,2016

4. Prevalence of bactericidal/permeability-increasing protein Autoantibodies in cystic fibrosis patients: systematic review and meta-analysis;Iwuji;Pediatr. Allergy Immunol. Pulmonol.,2019

5. Anti-neutrophil cytoplasmatic antibodies and lung disease in cystic fibrosis;Dorlochter;J. Cyst. Fibros.,2004

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