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Adventitial adaptive immune cells are associated with ascending aortic dilatation in patients with a bicuspid aortic valve

Authors :
Staal, Alexander H.J.
Cortenbach, Kimberley R.G.
Gorris, Mark A.J.
van der Woude, Lieke L.
Srinivas, Mangala
Heijmen, Robin H.
Geuzebroek, Guillaume S.C.
Grewal, Nimrat
Hebeda, Konnie M.
de Vries, I.J.M.
DeRuiter, Marco C.
van Kimmenade, Roland R.J.
Staal, Alexander H.J.
Cortenbach, Kimberley R.G.
Gorris, Mark A.J.
van der Woude, Lieke L.
Srinivas, Mangala
Heijmen, Robin H.
Geuzebroek, Guillaume S.C.
Grewal, Nimrat
Hebeda, Konnie M.
de Vries, I.J.M.
DeRuiter, Marco C.
van Kimmenade, Roland R.J.
Source :
ISSN: 2297-055X
Publication Year :
2023

Abstract

Background: Bicuspid aortic valve (BAV) is associated with ascending aorta aneurysms and dissections. Presently, genetic factors and pathological flow patterns are considered responsible for aneurysm formation in BAV while the exact role of inflammatory processes remains unknown. Methods: In order to objectify inflammation, we employ a highly sensitive, quantitative immunohistochemistry approach. Whole slides of dissected, dilated and non-dilated ascending aortas from BAV patients were quantitatively analyzed. Results: Dilated aortas show a 4-fold increase of lymphocytes and a 25-fold increase in B lymphocytes in the adventitia compared to non-dilated aortas. Tertiary lymphoid structures with B cell follicles and helper T cell expansion were identified in dilated and dissected aortas. Dilated aortas were associated with an increase in M1-like macrophages in the aorta media, in contrast the number of M2-like macrophages did not change significantly. Conclusion: This study finds unexpected large numbers of immune cells in dilating aortas of BAV patients. These findings raise the question whether immune cells in BAV aortopathy are innocent bystanders or contribute to the deterioration of the aortic wall.

Details

Database :
OAIster
Journal :
ISSN: 2297-055X
Notes :
application/pdf, Frontiers in Cardiovascular Medicine 10 (2023), ISSN: 2297-055X, ISSN: 2297-055X, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1394278296
Document Type :
Electronic Resource