scholarly journals Very Late Antigen-4: A Novel Receptor for Club Cell Secretory Protein 16 to Control Inflammation

Author(s):  
Hong Wei Chu ◽  
Niccolette Schaunaman
2016 ◽  
Vol 138 (3) ◽  
pp. 932-934.e1 ◽  
Author(s):  
Stefano Guerra ◽  
Monica M. Vasquez ◽  
Amber Spangenberg ◽  
Marilyn Halonen ◽  
Richard J. Martin

2018 ◽  
Vol 102 (8) ◽  
pp. 1382-1390 ◽  
Author(s):  
Angela Hin ◽  
Caroline Kannengiesser ◽  
Arnaud Roussel ◽  
Benjamin Renaud-Picard ◽  
Antoine Roux ◽  
...  

2018 ◽  
Vol 111 ◽  
pp. 109-116 ◽  
Author(s):  
Yun Zhou ◽  
Ge Mu ◽  
Yuewei Liu ◽  
Lili Xiao ◽  
Jixuan Ma ◽  
...  

2014 ◽  
Vol 68 ◽  
pp. 66-70 ◽  
Author(s):  
Eline B. Provost ◽  
Agnès Chaumont ◽  
Michal Kicinski ◽  
Bianca Cox ◽  
Frans Fierens ◽  
...  

2013 ◽  
Vol 20 (3) ◽  
pp. 180-182 ◽  
Author(s):  
Janice M Leung ◽  
Don D Sin

The inherent limitations of spirometry and clinical history have prompted clinicians and scientists to search for surrogate markers of airway diseases. Although few biomarkers have been widely accepted into the clinical armamentarium, the authors explore three sources of biomarkers that have shown promise as indicators of disease severity and treatment response. In asthma, exhaled nitric oxide measurements can predict steroid responsiveness and sputum eosinophil counts have been used to titrate anti-inflammatory therapies. In chronic obstructive pulmonary disease, inflammatory plasma biomarkers, such as fibrinogen, club cell secretory protein-16 and surfactant protein D, can denote greater severity and predict the risk of exacerbations. While the multitude of disease phenotypes in respiratory medicine make biomarker development especially challenging, these three may soon play key roles in the diagnosis and management of airway diseases.


2019 ◽  
Author(s):  
Stephen Milne ◽  
Xuan Li ◽  
Ana I Hernandez Cordero ◽  
Chen Xi Yang ◽  
Michael H Cho ◽  
...  

ABSTRACTBackgroundThere are currently no robust biomarkers of chronic obstructive pulmonary disease (COPD) risk or progression. Club cell secretory protein-16 (CC-16) is associated with the clinical expression of COPD. We aimed to determine if there is a causal effect of serum CC-16 level on COPD risk and/or progression using Mendelian randomisation (MR) analysis.MethodsWe performed a genome-wide association meta-analysis for serum CC-16 in two COPD cohorts (Lung Health Study [LHS], n=3,850 and ECLIPSE, n=1,702). We then used the CC-16-associated single-nucleotide polymorphisms (SNPs) in MR analysis to estimate the causal effect of serum CC-16 on COPD risk (International COPD Genetics Consortium/UK-Biobank dataset; n=35,735 cases, n=222,076 controls) and progression (change in forced expiratory volume in 1 s [FEV1] in LHS and ECLIPSE). We also determined the associations between SNPs associated with CC-16 and gene expression using n=1,111 lung tissue samples from the Lung eQTL Study.ResultsWe identified 7 SNPs independently associated (p<5×10−8) with serum CC-16 levels; 6 of these were novel. MR analysis suggested a protective causal effect of increased serum CC-16 on COPD risk (p=0.008) and progression (LHS only, p=0.02). Five of the SNPs were also associated with gene expression in lung tissue, including that of the CC-16-encoding gene SCGB1A1 (false discovery rate<0.1).ConclusionWe have identified several novel genetic variants associated with serum CC-16 level in COPD cohorts. These genetic associations suggest a potential causal effect of serum CC-16 on COPD risk and progression. Further investigation of CC-16 as a biomarker or therapeutic target in COPD is warranted.KEY MESSAGESWhat is the key question?Can genetics help uncover a causal effect of serum CC-16 level on COPD risk and/or progression?What is the bottom line?There is a protective effect of genetically-increased serum CC-16 on both COPD risk and progression (as measured by change in FEV1 over time), which may be due to increased expression of the CC-16-encoding gene SCGB1A1 in the lung.Why read on?This is the first study to demonstrate a possible causal effect of serum CC-16 in people with COPD, and highlights the potential for CC-16 as a biomarker or therapeutic target.


2015 ◽  
Vol 28 (3) ◽  
pp. 158-164 ◽  
Author(s):  
Christian Rosas-Salazar ◽  
Tebeb Gebretsadik ◽  
Kecia N. Carroll ◽  
Sara Reiss ◽  
Nancy Wickersham ◽  
...  

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