Cargando…

74 Secondary Immunohistochemical Analysis of Viable Cells as Determined by Hematoxylin and Eosin Staining

INTRODUCTION: Accurate clinical differentiation of deep partial-thickness (DPT) and full-thickness (FT) wounds is essential in justifying appropriate treatments for heterogeneous burns. Only recently has non-invasive burn depth imaging been ground-truthed with tissue punch biopsies; an endeavor that...

Descripción completa

Detalles Bibliográficos
Autores principales: Carney, Bonnie, D'Orio, Cameron, Shupp, Jeffrey, Carter, Jeffrey, Hickerson, William, Holmes, James, Phelan, Herbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185137/
http://dx.doi.org/10.1093/jbcr/irad045.048
_version_ 1785042287319842816
author Carney, Bonnie
D'Orio, Cameron
Shupp, Jeffrey
Carter, Jeffrey
Hickerson, William
Holmes, James
Phelan, Herbert
author_facet Carney, Bonnie
D'Orio, Cameron
Shupp, Jeffrey
Carter, Jeffrey
Hickerson, William
Holmes, James
Phelan, Herbert
author_sort Carney, Bonnie
collection PubMed
description INTRODUCTION: Accurate clinical differentiation of deep partial-thickness (DPT) and full-thickness (FT) wounds is essential in justifying appropriate treatments for heterogeneous burns. Only recently has non-invasive burn depth imaging been ground-truthed with tissue punch biopsies; an endeavor that will no doubt improve AI imaging algorithms in the near future. Prior literature supports unique apoptotic and necrotic properties of DPT and FT wounds, suggesting a use for not only standard stains (H&E), but apoptotic marker staining in assisting clinical diagnosis of burn depth, progression and/or conversion. METHODS: The aim of this study was to evaluate the presence of apoptotic cells in DPT and FT samples previously diagnosed by a burn biopsy algorithm (BBA-V2) for burn depth and severity by expert review of H&E-stained slides. Eight paired biopsies were collected from DPT and FT wounds in four patients within 72 hours of thermal injury and were immunofluorescently labeled for apoptosis markers by detection of deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) and cleaved caspase-3 (CC-3) staining. Fluorescence intensity in dermal appendages within images was used to quantify signal at 40x magnification for CC-3. % positive TUNEL cells were graded by an investigator blinded to the burn severity. A higher grade indicated higher % positivity. TUNEL grading was evaluated by Chi square test. CC-3 intensity was evaluated by Student’s t-test. RESULTS: Across all four patients, FT burns had higher levels of CC-3 in dermal appendages compared to DPT burns (Cy3:DAPI ratios: 1.53 ± 0.28 vs. 0.75 ± 0.13; p=0.1074). Within each patient, all FT biopsy sites had significantly higher levels of CC-3 versus DPT biopsy sites (p< 0.05)(Table). DPT burns had a greater proportion of patients with increasing grades of TUNEL positive cells (DPT: Grade 1: 16%, Grade 2: 36%, Grade 3: 48%; FT: Grade 1: 42.3%, Grade 2: 23.1%, Grade 3: 34.6%, p=0.1178). CONCLUSIONS: CC-3 and TUNEL levels within dermal appendages align with burn depth classification by H&E staining, wherein appendages graded as necrotic had higher levels of CC-3 and lower levels of TUNEL. Therefore, CC-3 and TUNEL are potential secondary histological markers for burn depth. Further analysis of isolated, individual dermal appendages is underway to identify what additional information this secondary marker may add to the diagnosis of burn depth. APPLICABILITY OF RESEARCH TO PRACTICE: For the first time there is access to a large tissue repository of biopsies from burn wounds. Although staining from these samples has been used to build diagnosis algorithms with success, much more can be learned from the cellular pathophysiology when secondary analyses are performed. These assays may help us understand the processes of burn conversion.
format Online
Article
Text
id pubmed-10185137
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-101851372023-05-16 74 Secondary Immunohistochemical Analysis of Viable Cells as Determined by Hematoxylin and Eosin Staining Carney, Bonnie D'Orio, Cameron Shupp, Jeffrey Carter, Jeffrey Hickerson, William Holmes, James Phelan, Herbert J Burn Care Res C-254 Correlative X: Translational Sciences: Wounds and Scars INTRODUCTION: Accurate clinical differentiation of deep partial-thickness (DPT) and full-thickness (FT) wounds is essential in justifying appropriate treatments for heterogeneous burns. Only recently has non-invasive burn depth imaging been ground-truthed with tissue punch biopsies; an endeavor that will no doubt improve AI imaging algorithms in the near future. Prior literature supports unique apoptotic and necrotic properties of DPT and FT wounds, suggesting a use for not only standard stains (H&E), but apoptotic marker staining in assisting clinical diagnosis of burn depth, progression and/or conversion. METHODS: The aim of this study was to evaluate the presence of apoptotic cells in DPT and FT samples previously diagnosed by a burn biopsy algorithm (BBA-V2) for burn depth and severity by expert review of H&E-stained slides. Eight paired biopsies were collected from DPT and FT wounds in four patients within 72 hours of thermal injury and were immunofluorescently labeled for apoptosis markers by detection of deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) and cleaved caspase-3 (CC-3) staining. Fluorescence intensity in dermal appendages within images was used to quantify signal at 40x magnification for CC-3. % positive TUNEL cells were graded by an investigator blinded to the burn severity. A higher grade indicated higher % positivity. TUNEL grading was evaluated by Chi square test. CC-3 intensity was evaluated by Student’s t-test. RESULTS: Across all four patients, FT burns had higher levels of CC-3 in dermal appendages compared to DPT burns (Cy3:DAPI ratios: 1.53 ± 0.28 vs. 0.75 ± 0.13; p=0.1074). Within each patient, all FT biopsy sites had significantly higher levels of CC-3 versus DPT biopsy sites (p< 0.05)(Table). DPT burns had a greater proportion of patients with increasing grades of TUNEL positive cells (DPT: Grade 1: 16%, Grade 2: 36%, Grade 3: 48%; FT: Grade 1: 42.3%, Grade 2: 23.1%, Grade 3: 34.6%, p=0.1178). CONCLUSIONS: CC-3 and TUNEL levels within dermal appendages align with burn depth classification by H&E staining, wherein appendages graded as necrotic had higher levels of CC-3 and lower levels of TUNEL. Therefore, CC-3 and TUNEL are potential secondary histological markers for burn depth. Further analysis of isolated, individual dermal appendages is underway to identify what additional information this secondary marker may add to the diagnosis of burn depth. APPLICABILITY OF RESEARCH TO PRACTICE: For the first time there is access to a large tissue repository of biopsies from burn wounds. Although staining from these samples has been used to build diagnosis algorithms with success, much more can be learned from the cellular pathophysiology when secondary analyses are performed. These assays may help us understand the processes of burn conversion. Oxford University Press 2023-05-15 /pmc/articles/PMC10185137/ http://dx.doi.org/10.1093/jbcr/irad045.048 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the American Burn Association. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle C-254 Correlative X: Translational Sciences: Wounds and Scars
Carney, Bonnie
D'Orio, Cameron
Shupp, Jeffrey
Carter, Jeffrey
Hickerson, William
Holmes, James
Phelan, Herbert
74 Secondary Immunohistochemical Analysis of Viable Cells as Determined by Hematoxylin and Eosin Staining
title 74 Secondary Immunohistochemical Analysis of Viable Cells as Determined by Hematoxylin and Eosin Staining
title_full 74 Secondary Immunohistochemical Analysis of Viable Cells as Determined by Hematoxylin and Eosin Staining
title_fullStr 74 Secondary Immunohistochemical Analysis of Viable Cells as Determined by Hematoxylin and Eosin Staining
title_full_unstemmed 74 Secondary Immunohistochemical Analysis of Viable Cells as Determined by Hematoxylin and Eosin Staining
title_short 74 Secondary Immunohistochemical Analysis of Viable Cells as Determined by Hematoxylin and Eosin Staining
title_sort 74 secondary immunohistochemical analysis of viable cells as determined by hematoxylin and eosin staining
topic C-254 Correlative X: Translational Sciences: Wounds and Scars
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185137/
http://dx.doi.org/10.1093/jbcr/irad045.048
work_keys_str_mv AT carneybonnie 74secondaryimmunohistochemicalanalysisofviablecellsasdeterminedbyhematoxylinandeosinstaining
AT doriocameron 74secondaryimmunohistochemicalanalysisofviablecellsasdeterminedbyhematoxylinandeosinstaining
AT shuppjeffrey 74secondaryimmunohistochemicalanalysisofviablecellsasdeterminedbyhematoxylinandeosinstaining
AT carterjeffrey 74secondaryimmunohistochemicalanalysisofviablecellsasdeterminedbyhematoxylinandeosinstaining
AT hickersonwilliam 74secondaryimmunohistochemicalanalysisofviablecellsasdeterminedbyhematoxylinandeosinstaining
AT holmesjames 74secondaryimmunohistochemicalanalysisofviablecellsasdeterminedbyhematoxylinandeosinstaining
AT phelanherbert 74secondaryimmunohistochemicalanalysisofviablecellsasdeterminedbyhematoxylinandeosinstaining