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Updated: Jun 4, 2026

Investigating Aortic Valve Calcification via Isolation and Culture of T Lymphocytes using Feeder Cells from Irradiated Buffy Coat
Published on: February 4, 2021
Blood vessels and lymphatics in calcific aortic stenosis--in support of its inflammatory pathogenesis
I Steiner1, L Krbal, J Dominik
1The Fingerland Department of Pathology, Charles University Faculty of Medicine and Faculty Hospital Hradec Králové, Czech Republic. steiner@lfhk.cuni.cz
Insights
Calcific aortic stenosis (CAS), a common heart valve disease, involves inflammation. This study found blood and lymphatic vessels with inflammatory cells in diseased aortic valves, supporting an inflammatory cause for CAS.
Area of Science:
- Cardiovascular Pathology
- Immunology
- Vascular Biology
Background:
- Calcific aortic stenosis (CAS) is the most prevalent acquired valvular heart disease in developed nations.
- CAS is increasingly recognized as an inflammatory process, akin to atherosclerosis.
- Etiologically, CAS is typically categorized as senile (degenerative) or related to a bicuspid aortic valve.
Purpose of the Study:
- To investigate the presence and significance of vascularization and inflammation within calcified aortic valve cusps.
- To compare the vascular and inflammatory patterns in senile versus bicuspid aortic valve types of CAS.
- To provide evidence supporting the inflammatory theory of CAS pathogenesis.
Main Methods:
- Histological examination and immunohistochemistry were performed on 28 human calcific aortic stenosis cases.
- Specific markers CD31 (for blood vessels) and D2-40 (for lymphatics) were utilized.
- Cases were classified into senile, bicuspid, or indeterminable types.
Main Results:
- Blood vessels were identified in all 28 examined calcified aortic valve cusps.
- Lymphatic vessels were present in 14 of the cases.
- Vascularization was consistently associated with lymphocytic infiltrates in 24 cases, irrespective of CAS type.
Conclusions:
- The presence of both blood and lymphatic vessels, alongside inflammatory cell infiltration, in calcified aortic cusps strongly supports an inflammatory mechanism in CAS pathogenesis.
- These findings contribute to understanding the etiology of this common valvular disease.
- The vascular and inflammatory patterns did not differ significantly between senile and bicuspid aortic valve types.
Abstract:
In developed countries, calcific aortic stenosis (CAS) has become the most common acquired valvular disease. It is considered a for of atherosclerosis and, like the latter, of inflammatory origin. Majority of cases of CAS are classified etiologically as either senile ("degenerative")--developing on previously normal aortic valve with three cusps, or based on congenitally malformed--bicuspid aortic valve. Twenty-eight cases of CAS (18 of the senile type, 7 of the bicuspid valve type, and 3 of indeterminable type) were examined by means of histology and immunohistochemistry (CD31 for blood vessels; D2-40 for lymphatics). In the calcified cusps, blood vessels were present in all 28 cases, and lymphatics in 14 of them. Vascularization was associated with lymphocytic infiltrates in 24 cases. There was no difference in the pattern between the two types of CAS. The origin of the cusp vessels is discussed. Our finding in the calcified cusps of both blood and lymphatic vessels together with lymphocytic infiltrates supports the inflammatory theory of the CAS pathogenesis.
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