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Anti-BPIFA1/SPLUNC1: a new autoantibody prevalent in patients with endstage cystic fibrosis.
- Source :
-
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society [J Cyst Fibros] 2014 May; Vol. 13 (3), pp. 281-8. Date of Electronic Publication: 2013 Oct 23. - Publication Year :
- 2014
-
Abstract
- Background: Bactericidal/permeability increasing protein fold containing family A (BPIFA) 1, is a secreted protein of the upper airways that shares structural homology with BPI and exhibits comparable antimicrobial capacities. We hypothesized that CF patients have circulating IgG or IgA anti-BPIFA1 autoantibodies, similarly as reported for BPI autoantibodies.<br />Methods: We analyzed pre- and post-transplantation sera from 67 endstage lung disease patients who underwent lung transplantation (LTx) because of COPD (n=27), CF (n=25), and ILD (n=15).<br />Results: Anti-BPIFA1 (48%) and anti-BPI (92%) were elevated in CF patients compared to healthy controls, with anti-BPIFA1 IgG isotype being most prevalent, whereas anti-BPI is of the IgA isotype. Levels of anti-BPI autoantibodies significantly declined post-LTx, whereas anti-BPIFA1 did not. No relation was found between autoantibodies against BPIFA1 and BPI.<br />Conclusion: Our results indicate that BPIFA1 is a novel target for autoantibodies in CF. The function of these autoantibodies needed to be investigated in future studies.<br /> (© 2013.)
- Subjects :
- Adolescent
Adult
Cohort Studies
Cystic Fibrosis epidemiology
Cystic Fibrosis surgery
Female
Homeodomain Proteins immunology
Humans
Immunoglobulin A immunology
Immunoglobulin G immunology
Lung Transplantation
Male
Middle Aged
Pulmonary Disease, Chronic Obstructive epidemiology
Pulmonary Disease, Chronic Obstructive surgery
Rheumatoid Factor immunology
Seroepidemiologic Studies
Transcription Factors immunology
Young Adult
Autoantibodies immunology
Cystic Fibrosis immunology
Glycoproteins immunology
Phosphoproteins immunology
Pulmonary Disease, Chronic Obstructive immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1873-5010
- Volume :
- 13
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
- Publication Type :
- Academic Journal
- Accession number :
- 24269518
- Full Text :
- https://doi.org/10.1016/j.jcf.2013.10.005