期刊
JOURNAL OF HEART AND LUNG TRANSPLANTATION
卷 29, 期 5, 页码 538-543出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.healun.2009.10.007
关键词
heart valve bioprostheses; immunogenicity; calcification; alpha-gal; anti-gal antibodies
资金
- University of Paris Descartes, Assistance Publique Hopitaux de Paris
- Alain Carpentier Foundation
BACKGROUND: Although glutaraldehyde fixation is known to reduce immunogenicity and degeneration of heart valve bioprostheses, some degree of immunogenicity persists, which may trigger calcification. The aims of this study were to: (1) define the role of alpha-1,3-galactosyltransferase (alpha-Gal) antigen in valve calcification by comparing alpha-Gal-positive and alpha-Gal-deficient (GT-KO) pig pericardium; and (2) elucidate the role of human anti-Gal antibodies in the process of calcification and to determine the potential influence of different tissue-fixation techniques. METHODS: Glutaraldehyde-treated pericardium from alpha-Gal-positive and GT-KO pigs, with or without pre-labeling with human anti-Gal antibodies, were implanted in rats during I month. RESULTS: In glutaraldehyde-fixed pericardium, calcification levels were significantly lower in GT-KO pig pericardium (132.8 +/- 5.8 mu g/mg) as compared with alpha-Gal-positive pig pericardium (155.7 +/- 7.1 mu g/mg) (p < 0.015). In glutaraldehyde-fixed pig pericardium followed by a mix of formaldehyde, ethanol and Tween 80 (FET), the calcification levels were lower in GT-KO pig pericardium (0.35 +/- 0.1 mu g/mg) as compared with alpha-Gal-positive pig pericardium (4.6 +/- 4.2 mu g/mg). In glutaraldehyde-fixed pig pericardium + FET pre-incubated with human anti-Gal antibodies, calcification levels were significantly greater in mu-Gal-positive pig pericardium (43.8 +/- 8.5 mu g/mg) as compared with GT-KO pig pericardium (5.7 +/- 2.9 mu g/mg) (p < 0.0001). CONCLUSIONS: This study demonstrates the role of alpha-Gal antigen and human alpha-Gal antibodies in the calcification process of valvular bioprostheses. It is suggested that GT-KO pig pericardium could be beneficial as a new source of material for heart valve bioprostheses. J Heart Lung Transplant 2010;29:538-543 (C) 2010 International Society for Heart and Lung Transplantation. All rights reserved.
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