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Histopathological Lung Findings in COVID-19 B.1.617.2 SARS-CoV-2 Delta Variant

Background: The Delta variant (Pango lineage B.1.617.2) is one of the most significant and aggressive variants of SARS-CoV-2. To the best of our knowledge, this is the first paper specifically studying pulmonary morphopathology in COVID-19 caused by the B.1.617.2 Delta variant. Methods: The study in...

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Autores principales: Jeican, Ionuț Isaia, Inișca, Patricia, Gheban, Dan, Anton, Vlad, Lazăr, Mihaela, Vică, Mihaela Laura, Mironescu, Daniela, Rebeleanu, Codrin, Crivii, Carmen Bianca, Aluaș, Maria, Albu, Silviu, Siserman, Costel Vasile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9961426/
https://www.ncbi.nlm.nih.gov/pubmed/36836513
http://dx.doi.org/10.3390/jpm13020279
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author Jeican, Ionuț Isaia
Inișca, Patricia
Gheban, Dan
Anton, Vlad
Lazăr, Mihaela
Vică, Mihaela Laura
Mironescu, Daniela
Rebeleanu, Codrin
Crivii, Carmen Bianca
Aluaș, Maria
Albu, Silviu
Siserman, Costel Vasile
author_facet Jeican, Ionuț Isaia
Inișca, Patricia
Gheban, Dan
Anton, Vlad
Lazăr, Mihaela
Vică, Mihaela Laura
Mironescu, Daniela
Rebeleanu, Codrin
Crivii, Carmen Bianca
Aluaș, Maria
Albu, Silviu
Siserman, Costel Vasile
author_sort Jeican, Ionuț Isaia
collection PubMed
description Background: The Delta variant (Pango lineage B.1.617.2) is one of the most significant and aggressive variants of SARS-CoV-2. To the best of our knowledge, this is the first paper specifically studying pulmonary morphopathology in COVID-19 caused by the B.1.617.2 Delta variant. Methods: The study included 10 deceased patients (40-83 years) with the COVID-19 Delta variant. The necrotic lung fragments were obtained either by biopsy (six cases) or autopsy (four cases). Tissue samples were subjected to virology analysis for identification of the SARS-CoV-2 variant, histopathology, and immunohistochemistry (anti-SARS coronavirus mouse anti-virus antibody). Results: Virology analysis identified B.1.617.2 through genetic sequencing in eight cases, and in two cases, specific mutations of B.1.617.2 were identified. Macroscopically, in all autopsied cases, the lung had a particular appearance, purple in color, with increased consistency on palpation and abolished crepitations. Histopathologically, the most frequently observed lesions were acute pulmonary edema (70%) and diffuse alveolar damage at different stages. The immunohistochemical examination was positive for proteins of SARS-CoV-2 in 60% of cases on alveolocytes and in endothelial cells. Conclusions: The histopathological lung findings in the B.1.617.2 Delta variant are similar to those previously described in COVID-19. Spike protein-binding antibodies were identified immunohistochemically both on alveolocytes and in the endothelial cells, showing the potential of indirect damage from thrombosis.
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spelling pubmed-99614262023-02-26 Histopathological Lung Findings in COVID-19 B.1.617.2 SARS-CoV-2 Delta Variant Jeican, Ionuț Isaia Inișca, Patricia Gheban, Dan Anton, Vlad Lazăr, Mihaela Vică, Mihaela Laura Mironescu, Daniela Rebeleanu, Codrin Crivii, Carmen Bianca Aluaș, Maria Albu, Silviu Siserman, Costel Vasile J Pers Med Article Background: The Delta variant (Pango lineage B.1.617.2) is one of the most significant and aggressive variants of SARS-CoV-2. To the best of our knowledge, this is the first paper specifically studying pulmonary morphopathology in COVID-19 caused by the B.1.617.2 Delta variant. Methods: The study included 10 deceased patients (40-83 years) with the COVID-19 Delta variant. The necrotic lung fragments were obtained either by biopsy (six cases) or autopsy (four cases). Tissue samples were subjected to virology analysis for identification of the SARS-CoV-2 variant, histopathology, and immunohistochemistry (anti-SARS coronavirus mouse anti-virus antibody). Results: Virology analysis identified B.1.617.2 through genetic sequencing in eight cases, and in two cases, specific mutations of B.1.617.2 were identified. Macroscopically, in all autopsied cases, the lung had a particular appearance, purple in color, with increased consistency on palpation and abolished crepitations. Histopathologically, the most frequently observed lesions were acute pulmonary edema (70%) and diffuse alveolar damage at different stages. The immunohistochemical examination was positive for proteins of SARS-CoV-2 in 60% of cases on alveolocytes and in endothelial cells. Conclusions: The histopathological lung findings in the B.1.617.2 Delta variant are similar to those previously described in COVID-19. Spike protein-binding antibodies were identified immunohistochemically both on alveolocytes and in the endothelial cells, showing the potential of indirect damage from thrombosis. MDPI 2023-01-31 /pmc/articles/PMC9961426/ /pubmed/36836513 http://dx.doi.org/10.3390/jpm13020279 Text en © 2023 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
Jeican, Ionuț Isaia
Inișca, Patricia
Gheban, Dan
Anton, Vlad
Lazăr, Mihaela
Vică, Mihaela Laura
Mironescu, Daniela
Rebeleanu, Codrin
Crivii, Carmen Bianca
Aluaș, Maria
Albu, Silviu
Siserman, Costel Vasile
Histopathological Lung Findings in COVID-19 B.1.617.2 SARS-CoV-2 Delta Variant
title Histopathological Lung Findings in COVID-19 B.1.617.2 SARS-CoV-2 Delta Variant
title_full Histopathological Lung Findings in COVID-19 B.1.617.2 SARS-CoV-2 Delta Variant
title_fullStr Histopathological Lung Findings in COVID-19 B.1.617.2 SARS-CoV-2 Delta Variant
title_full_unstemmed Histopathological Lung Findings in COVID-19 B.1.617.2 SARS-CoV-2 Delta Variant
title_short Histopathological Lung Findings in COVID-19 B.1.617.2 SARS-CoV-2 Delta Variant
title_sort histopathological lung findings in covid-19 b.1.617.2 sars-cov-2 delta variant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9961426/
https://www.ncbi.nlm.nih.gov/pubmed/36836513
http://dx.doi.org/10.3390/jpm13020279
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