Can secretory immunoglobulin A in saliva predict a change in lung infection status in patients with cystic fibrosis? A prospective pilot study-Reference-Cited by-同舟云学术

Can secretory immunoglobulin A in saliva predict a change in lung infection status in patients with cystic fibrosis? A prospective pilot study

Published:2018-07-12 Issue:8 Volume:1 Page:e52
ISSN:2398-8835
Container-title:Health Science Reports
language:en
Short-container-title:Health Sci Rep

Author:

Alanin Mikkel Christian¹^ORCID,Pressler Tania²,Aanaes Kasper¹,Ekstrøm Claus Thorn³,Skov Marianne²,Johansen Helle Krogh⁴,Nielsen Kim G.²⁵,von Buchwald Christian¹,Høiby Niels⁴⁶

Affiliation:

1. Department of Otorhinolaryngology, Head and Neck Surgery and Audiology; Rigshospitalet; Denmark

2. Copenhagen CF Centre; Rigshospitalet; Denmark

3. Section of Biostatistics; University of Copenhagen; Denmark

4. Department of Clinical Microbiology; Rigshospitalet; Denmark

5. Paediatric Pulmonary Service; Rigshospitalet, University of Copenhagen; Denmark

6. Institute of Immunology and Microbiology, University of Copenhagen; Denmark

Funder

Seventh Framework Programme

Novo Nordisk Fonden

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/hsr2.52/fullpdf

Reference20 articles.

1. Pseudomonas aeruginosa biofilms in the respiratory tract of cystic fibrosis patients;Bjarnsholt;Pediatr Pulmonol,2009

2. Seasonal onset of initial colonisation and chronic infection with Pseudomonas aeruginosa in patients with cystic fibrosis in Denmark;Johansen;Thorax,1992

3. Antibiotic treatment of initial colonization with Pseudomonas aeruginosa postpones chronic infection and prevents deterioration of pulmonary function in cystic fibrosis;Frederiksen;Pediatr Pulmonol,1997

4. Early rise of anti-pseudomonas antibodies and a mucoid phenotype of pseudomonas aeruginosa are risk factors for development of chronic lung infection-a case control study;Pressler;J Cyst Fibros,2006

5. Antibody response to Pseudomonas aeruginosa in cystic fibrosis patients: a marker of therapeutic success?-a 30-year cohort study of survival in Danish CF patients after onset of chronic P. aeruginosa lung infection;Johansen;Pediatr Pulmonol,2004

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. What diagnostic tests are available for respiratory infections or pulmonary exacerbations in cystic fibrosis: A scoping literature review;Respiratory Investigation;2024-09

2. The criteria for chronic rhinosinusitis in children with cystic fibrosis are rarely fulfilled after initiation of CFTR modulator treatment;APMIS;2024-05-21

3. Dental caries and associated salivary biomarkers in patients with cystic fibrosis;Pediatric Pulmonology;2022-09-19

4. Role of Salivary Biomarkers in Cystic Fibrosis: A Systematic Review;BioMed Research International;2022-01-19

5. Simultaneous capillary electrophoresis of anions and cations in a single injection using an anion exchanger-modified capillary for determination of salivary ions in combination with statistical analyses;Journal of Chromatography A;2021-01