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Inflammatory immune response in recipients of transcatheter aortic valves

OBJECTIVE: Transcatheter aortic valve implantation (TAVI) is rapidly replacing cardiac surgery due to its minimal invasiveness and practicality. Midterm immunological studies on the biocompatibility of galactose-alpha-1,3-galactose (α-Gal)–carrying bioprosthetic heart valves for TAVI are not availab...

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Autores principales: Veraar, Cecilia, Koschutnik, Matthias, Nitsche, Christian, Laggner, Maria, Polak, Dominika, Bohle, Barbara, Mangold, Andreas, Moser, Bernhard, Mascherbauer, Julia, Ankersmit, Hendrik J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9390500/
https://www.ncbi.nlm.nih.gov/pubmed/36003560
http://dx.doi.org/10.1016/j.xjon.2021.02.012
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author Veraar, Cecilia
Koschutnik, Matthias
Nitsche, Christian
Laggner, Maria
Polak, Dominika
Bohle, Barbara
Mangold, Andreas
Moser, Bernhard
Mascherbauer, Julia
Ankersmit, Hendrik J.
author_facet Veraar, Cecilia
Koschutnik, Matthias
Nitsche, Christian
Laggner, Maria
Polak, Dominika
Bohle, Barbara
Mangold, Andreas
Moser, Bernhard
Mascherbauer, Julia
Ankersmit, Hendrik J.
author_sort Veraar, Cecilia
collection PubMed
description OBJECTIVE: Transcatheter aortic valve implantation (TAVI) is rapidly replacing cardiac surgery due to its minimal invasiveness and practicality. Midterm immunological studies on the biocompatibility of galactose-alpha-1,3-galactose (α-Gal)–carrying bioprosthetic heart valves for TAVI are not available. In this study we investigated whether bioprosthetic heart valves employed for TAVI augment an α-Gal–specific antibody-dependent and antibody-independent immune response 3 months after TAVI implantation. METHODS: This prospective observational study included 27 patients with severe aortic valve stenosis undergoing TAVI and 10 patients with severe mitral valve regurgitation treated with a transcatheter MitraClip (Abbott Laboratories, Abbott Park, Ill) procedure. Blood samples were drawn before and 90 days after treatment at a routine checkup. Serum samples were analyzed using enzyme-linked immunosorbent assay. Serum concentrations of α-Gal–specific immunoglobulin (Ig) G, IgG subclasses and IgE, complement factor 3a, NETosis-specific citrullinated H3, and the systemic inflammation markers soluble suppression of tumorigenicity and interleukin 33 were evaluated. RESULTS: Three months after TAVI, we found significantly increased serum concentrations of α-Gal–specific IgG3, complement factor complement factor 3a, citrullinated H3 levels, and soluble suppression of tumorigenicity (P = .002, P = .001, P = .025, and P = .039, respectively). Sensitization of α-Gal–specific IgE antibodies occurred in 55% of all patients after TAVI. CONCLUSIONS: Our results indicate that TAVI elicits a midterm, specific humoral immune response against α-Gal and causes an unspecific humoral inflammation compared with patients undergoing MitraClip implantation. This observation will lead to a better understanding of postintervention morbidity and the long-term durability of bioprostheses and indicates that caution is appropriate when designing implantation strategies for younger patients.
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spelling pubmed-93905002022-08-23 Inflammatory immune response in recipients of transcatheter aortic valves Veraar, Cecilia Koschutnik, Matthias Nitsche, Christian Laggner, Maria Polak, Dominika Bohle, Barbara Mangold, Andreas Moser, Bernhard Mascherbauer, Julia Ankersmit, Hendrik J. JTCVS Open Adult: Aortic Valve: Basic Science OBJECTIVE: Transcatheter aortic valve implantation (TAVI) is rapidly replacing cardiac surgery due to its minimal invasiveness and practicality. Midterm immunological studies on the biocompatibility of galactose-alpha-1,3-galactose (α-Gal)–carrying bioprosthetic heart valves for TAVI are not available. In this study we investigated whether bioprosthetic heart valves employed for TAVI augment an α-Gal–specific antibody-dependent and antibody-independent immune response 3 months after TAVI implantation. METHODS: This prospective observational study included 27 patients with severe aortic valve stenosis undergoing TAVI and 10 patients with severe mitral valve regurgitation treated with a transcatheter MitraClip (Abbott Laboratories, Abbott Park, Ill) procedure. Blood samples were drawn before and 90 days after treatment at a routine checkup. Serum samples were analyzed using enzyme-linked immunosorbent assay. Serum concentrations of α-Gal–specific immunoglobulin (Ig) G, IgG subclasses and IgE, complement factor 3a, NETosis-specific citrullinated H3, and the systemic inflammation markers soluble suppression of tumorigenicity and interleukin 33 were evaluated. RESULTS: Three months after TAVI, we found significantly increased serum concentrations of α-Gal–specific IgG3, complement factor complement factor 3a, citrullinated H3 levels, and soluble suppression of tumorigenicity (P = .002, P = .001, P = .025, and P = .039, respectively). Sensitization of α-Gal–specific IgE antibodies occurred in 55% of all patients after TAVI. CONCLUSIONS: Our results indicate that TAVI elicits a midterm, specific humoral immune response against α-Gal and causes an unspecific humoral inflammation compared with patients undergoing MitraClip implantation. This observation will lead to a better understanding of postintervention morbidity and the long-term durability of bioprostheses and indicates that caution is appropriate when designing implantation strategies for younger patients. Elsevier 2021-03-12 /pmc/articles/PMC9390500/ /pubmed/36003560 http://dx.doi.org/10.1016/j.xjon.2021.02.012 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Adult: Aortic Valve: Basic Science
Veraar, Cecilia
Koschutnik, Matthias
Nitsche, Christian
Laggner, Maria
Polak, Dominika
Bohle, Barbara
Mangold, Andreas
Moser, Bernhard
Mascherbauer, Julia
Ankersmit, Hendrik J.
Inflammatory immune response in recipients of transcatheter aortic valves
title Inflammatory immune response in recipients of transcatheter aortic valves
title_full Inflammatory immune response in recipients of transcatheter aortic valves
title_fullStr Inflammatory immune response in recipients of transcatheter aortic valves
title_full_unstemmed Inflammatory immune response in recipients of transcatheter aortic valves
title_short Inflammatory immune response in recipients of transcatheter aortic valves
title_sort inflammatory immune response in recipients of transcatheter aortic valves
topic Adult: Aortic Valve: Basic Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9390500/
https://www.ncbi.nlm.nih.gov/pubmed/36003560
http://dx.doi.org/10.1016/j.xjon.2021.02.012
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