Calcific aortic valve stenosis: Immunohistochemical analysis of inflammatory infiltrate
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22436689
DOI
10.1016/j.prp.2012.02.009
PII: S0344-0338(12)00045-3
Knihovny.cz E-resources
- MeSH
- Aortic Valve metabolism pathology surgery MeSH
- Aortic Valve Stenosis metabolism pathology surgery MeSH
- B-Lymphocytes metabolism pathology MeSH
- Biomarkers metabolism MeSH
- Antigens, CD metabolism MeSH
- Histiocytes metabolism pathology MeSH
- Immune System metabolism pathology MeSH
- Immunoglobulins metabolism MeSH
- Calcinosis metabolism pathology surgery MeSH
- Humans MeSH
- Mast Cells metabolism pathology MeSH
- Neovascularization, Pathologic pathology MeSH
- Plasma Cells metabolism pathology MeSH
- Aged MeSH
- T-Lymphocytes metabolism pathology MeSH
- Inflammation metabolism pathology MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers MeSH
- Antigens, CD MeSH
- Immunoglobulins MeSH
Calcific aortic valve disease is considered a form of atherosclerosis and, like the latter, possibly of inflammatory origin. The aim of our work was to study the pattern of cellular infiltrate in calcific aortic valve stenosis (CAS). Fifteen operatively excised calcified aortic valves were examined by histology and immunohistochemistry (CD20, CD79α, CD3, CD4, CD8, CD68, CD138, CD117, BJK, BJL, IgA, IgD, IgG, IgG4 and IgM). The findings revealed that in CAS, there were chronic inflammatory features with infiltrates comprising lymphocytes, polyclonal plasma cells, histiocytes and mast cells. In T-lymphocytes, CD4 prevailed over CD8. In B-lymphocytes, there was a slight preponderance of CD20 over CD79α. The BJL (lambda)-positive plasma cells prevailed over the BJK (kappa) ones. The CD138-positive plasma cells comprised 24% IgA-, 20% IgD-, 41% IgG- (including 11% of IgG4-) and 15% IgM-positive cells. CAS did not fulfill the criteria of the recently described clinicopathological entity IgG4-related sclerosing systemic disease. The inflammatory process was the same in both subsets of CAS - those with trileaflet (normally formed) valves and those with congenitally bicuspid valves.
References provided by Crossref.org