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Technical note on the exploration of COVID-19 in autopsy material

Interrogation of immune response in autopsy material from patients with SARS-CoV-2 is potentially significant. We aim to describe a validated protocol for the exploration of the molecular physiopathology of SARS-CoV-2 pulmonary disease using multiplex immunofluorescence (mIF). The application of val...

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Detalles Bibliográficos
Autores principales: Humphries, Matthew Phillip, Bingham, Victoria, Abdullah Sidi, Fatima, Craig, Stephanie, Lara, Beatrize, El-daly, Hesham, O'Doherty, Nicole, Maxwell, Perry, Lewis, Claire, McQuaid, Stephen, Lyness, James, James, Jacqueline, Snead, David R J, Salto-Tellez, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313984/
https://www.ncbi.nlm.nih.gov/pubmed/36717223
http://dx.doi.org/10.1136/jcp-2022-208525
Descripción
Sumario:Interrogation of immune response in autopsy material from patients with SARS-CoV-2 is potentially significant. We aim to describe a validated protocol for the exploration of the molecular physiopathology of SARS-CoV-2 pulmonary disease using multiplex immunofluorescence (mIF). The application of validated assays for the detection of SARS-CoV-2 in tissues, originally developed in our laboratory in the context of oncology, was used to map the topography and complexity of the adaptive immune response at protein and mRNA levels. SARS-CoV-2 is detectable in situ by protein or mRNA, with a sensitivity that could be in part related to disease stage. In formalin-fixed, paraffin-embedded pneumonia material, multiplex immunofluorescent panels are robust, reliable and quantifiable and can detect topographic variations in inflammation related to pathological processes. Clinical autopsies have relevance in understanding diseases of unknown/complex pathophysiology. In particular, autopsy materials are suitable for the detection of SARS-CoV-2 and for the topographic description of the complex tissue-based immune response using mIF.