Authors
Kevin Budding, Eduard A van de Graaf, Tineke Kardol-Hoefnagel, Johanna M Kwakkel-van Erp, Diana A van Kessel, Duska A Dragun, Cornelis E Hack, Henderikus G Otten
Publication date
2016
Journal
Chronic Lung Allograft Dysfunction After Lung Transplantation
Volume
14
Issue
1
Pages
115
Description
Autoantibodies against endothelin-1 type A receptor (ETAR) are present in systemic sclerosis complicated by lung fibrosis and pulmonary hypertension. As increased serum levels and local overproduction of endothelin-1 in the airways is reported in cystic fibrosis (CF) patients, we reasoned that anti-ETAR antibodies could be prevalent in endstage CF patients prior to lung transplantation (LTx). Also, ETAR autoantibodies are frequently associated with autoantibodies against the angiotensin II type 1 receptor (AT1R). We analyzed the presence of anti-ETAR and anti-AT1R autoantibodies in 43 LTx patients (chronic obstructive pulmonary disease (COPD), n= 20; CF, n= 13; interstitial lung disease (ILD), n= 1. We observed overall higher anti-ETAR and anti-AT1R autoantibody titers in sera taken prior to LTx in the CF patient group compared to COPD. No difference was found in autoantibody levels between patients with CF versus ILD. In sera taken post-LTx we found the same difference in anti-ETAR and anti-AT1R autoantibody titers between patients with CF versus COPD. No difference was found in antibody titers between sera taken prior to or 6 months after LTx. There was no association between autoantibody levels and other relevant demographic parameters, and we found no association between autoantibody titers and the development of the bronchiolitis obliterans syndrome. Both autoantibody titers were strongly correlated. We hypothesize that due to prolonged exposure to bacterial infection, increased levels of AT1R and ETAR result in a deregulated immune response causing autoantibody formation. Further research is expedient to …
Scholar articles
K Budding, EA van de Graaf, T Kardol-Hoefnagel… - Chronic Lung Allograft Dysfunction After Lung …, 2016