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Antigenicity Preservation Is Related to Tissue Characteristics and the Post-Mortem Interval: Immunohistochemical Study and Literature Review

The main aim of this study was to investigate the post-mortem proteolytic degradation process of selected tissue antigens and correlate it to the post-mortem interval. During the autopsy of 12 cadavers (time interval ranging 1 day–2 years after death) samples of skin, liver, kidney, and spleen were...

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Autores principales: Mauriello, Silvestro, Treglia, Michele, Pallocci, Margherita, Bonfiglio, Rita, Giacobbi, Erica, Passalacqua, Pierluigi, Cammarano, Andrea, D’Ovidio, Cristian, Marsella, Luigi Tonino, Scimeca, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408092/
https://www.ncbi.nlm.nih.gov/pubmed/36011152
http://dx.doi.org/10.3390/healthcare10081495
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author Mauriello, Silvestro
Treglia, Michele
Pallocci, Margherita
Bonfiglio, Rita
Giacobbi, Erica
Passalacqua, Pierluigi
Cammarano, Andrea
D’Ovidio, Cristian
Marsella, Luigi Tonino
Scimeca, Manuel
author_facet Mauriello, Silvestro
Treglia, Michele
Pallocci, Margherita
Bonfiglio, Rita
Giacobbi, Erica
Passalacqua, Pierluigi
Cammarano, Andrea
D’Ovidio, Cristian
Marsella, Luigi Tonino
Scimeca, Manuel
author_sort Mauriello, Silvestro
collection PubMed
description The main aim of this study was to investigate the post-mortem proteolytic degradation process of selected tissue antigens and correlate it to the post-mortem interval. During the autopsy of 12 cadavers (time interval ranging 1 day–2 years after death) samples of skin, liver, kidney, and spleen were collected. All samples were formalin-fixed and paraffin-embedded. Four µm paraffin sections were used for hematoxylin–eosin staining and immunohistochemical analysis (Ki67, Vimentin, Pan cytokeratin, and CD20). Data reported here show that immunohistochemical reactivity preservation was related to the characteristics of the tissues. In particular, the most resistant tissue was the skin, where the autolysis phenomena were not appreciable before 5 days. On the contrary, the liver and the spleen underwent early autolysis, while the kidney displayed an early autolysis of the tubules and a late one of the glomeruli. As concerns specific antigens, immunoreactivity was lost earliest for nuclear antigens as compared to cytoplasmic ones. In conclusion, our results demonstrate that immunohistochemical detection of specific antigens may be useful in estimating the post-mortem interval, especially when we need to know whether the post-mortem interval is a few days or more than 7–10 days.
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spelling pubmed-94080922022-08-26 Antigenicity Preservation Is Related to Tissue Characteristics and the Post-Mortem Interval: Immunohistochemical Study and Literature Review Mauriello, Silvestro Treglia, Michele Pallocci, Margherita Bonfiglio, Rita Giacobbi, Erica Passalacqua, Pierluigi Cammarano, Andrea D’Ovidio, Cristian Marsella, Luigi Tonino Scimeca, Manuel Healthcare (Basel) Article The main aim of this study was to investigate the post-mortem proteolytic degradation process of selected tissue antigens and correlate it to the post-mortem interval. During the autopsy of 12 cadavers (time interval ranging 1 day–2 years after death) samples of skin, liver, kidney, and spleen were collected. All samples were formalin-fixed and paraffin-embedded. Four µm paraffin sections were used for hematoxylin–eosin staining and immunohistochemical analysis (Ki67, Vimentin, Pan cytokeratin, and CD20). Data reported here show that immunohistochemical reactivity preservation was related to the characteristics of the tissues. In particular, the most resistant tissue was the skin, where the autolysis phenomena were not appreciable before 5 days. On the contrary, the liver and the spleen underwent early autolysis, while the kidney displayed an early autolysis of the tubules and a late one of the glomeruli. As concerns specific antigens, immunoreactivity was lost earliest for nuclear antigens as compared to cytoplasmic ones. In conclusion, our results demonstrate that immunohistochemical detection of specific antigens may be useful in estimating the post-mortem interval, especially when we need to know whether the post-mortem interval is a few days or more than 7–10 days. MDPI 2022-08-08 /pmc/articles/PMC9408092/ /pubmed/36011152 http://dx.doi.org/10.3390/healthcare10081495 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mauriello, Silvestro
Treglia, Michele
Pallocci, Margherita
Bonfiglio, Rita
Giacobbi, Erica
Passalacqua, Pierluigi
Cammarano, Andrea
D’Ovidio, Cristian
Marsella, Luigi Tonino
Scimeca, Manuel
Antigenicity Preservation Is Related to Tissue Characteristics and the Post-Mortem Interval: Immunohistochemical Study and Literature Review
title Antigenicity Preservation Is Related to Tissue Characteristics and the Post-Mortem Interval: Immunohistochemical Study and Literature Review
title_full Antigenicity Preservation Is Related to Tissue Characteristics and the Post-Mortem Interval: Immunohistochemical Study and Literature Review
title_fullStr Antigenicity Preservation Is Related to Tissue Characteristics and the Post-Mortem Interval: Immunohistochemical Study and Literature Review
title_full_unstemmed Antigenicity Preservation Is Related to Tissue Characteristics and the Post-Mortem Interval: Immunohistochemical Study and Literature Review
title_short Antigenicity Preservation Is Related to Tissue Characteristics and the Post-Mortem Interval: Immunohistochemical Study and Literature Review
title_sort antigenicity preservation is related to tissue characteristics and the post-mortem interval: immunohistochemical study and literature review
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408092/
https://www.ncbi.nlm.nih.gov/pubmed/36011152
http://dx.doi.org/10.3390/healthcare10081495
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