SARS-CoV-2 Detection by Digital Polymerase Chain Reaction and Immunohistochemistry in Skin Biopsies from 52 Patients with Different COVID-19-Associated Cutaneous Phenotypes.


Journal

Dermatology (Basel, Switzerland)
ISSN: 1421-9832
Titre abrégé: Dermatology
Pays: Switzerland
ID NLM: 9203244

Informations de publication

Date de publication:
2023
Historique:
received: 31 03 2022
accepted: 11 04 2023
medline: 7 8 2023
pubmed: 20 4 2023
entrez: 19 04 2023
Statut: ppublish

Résumé

COronaVIrus Disease 19 (COVID-19) is associated with a wide spectrum of skin manifestations, but SARS-CoV-2 RNA in lesional skin has been demonstrated only in few cases. The objective of this study was to demonstrate SARS-CoV-2 presence in skin samples from patients with different COVID-19-related cutaneous phenotypes. Demographic and clinical data from 52 patients with COVID-19-associated cutaneous manifestations were collected. Immunohistochemistry and digital PCR (dPCR) were performed in all skin samples. RNA in situ hybridization (ISH) was used to confirm the presence of SARS-CoV-2 RNA. Twenty out of 52 (38%) patients presented SARS-CoV-2 positivity in the skin. Among these, 10/52 (19%) patients tested positive for spike protein on immunohistochemistry, five of whom had also positive testing on dPCR. Of the latter, one tested positive both for ISH and ACE-2 on immunohistochemistry while another one tested positive for nucleocapsid protein. Twelve patients showed positivity only for nucleocapsid protein on immunohistochemistry. SARS-CoV-2 was detected only in 38% of patients, without any association with a specific cutaneous phenotype, suggesting that the pathophysiology of cutaneous lesions mostly depends on the activation of the immune system. The combination of spike and nucleocapsid immunohistochemistry has higher diagnostic yield than dPCR. Skin persistence of SARS-CoV-2 may depend on timing of skin lesions, viral load, and immune response.

Sections du résumé

BACKGROUND BACKGROUND
COronaVIrus Disease 19 (COVID-19) is associated with a wide spectrum of skin manifestations, but SARS-CoV-2 RNA in lesional skin has been demonstrated only in few cases.
OBJECTIVE OBJECTIVE
The objective of this study was to demonstrate SARS-CoV-2 presence in skin samples from patients with different COVID-19-related cutaneous phenotypes.
METHODS METHODS
Demographic and clinical data from 52 patients with COVID-19-associated cutaneous manifestations were collected. Immunohistochemistry and digital PCR (dPCR) were performed in all skin samples. RNA in situ hybridization (ISH) was used to confirm the presence of SARS-CoV-2 RNA.
RESULTS RESULTS
Twenty out of 52 (38%) patients presented SARS-CoV-2 positivity in the skin. Among these, 10/52 (19%) patients tested positive for spike protein on immunohistochemistry, five of whom had also positive testing on dPCR. Of the latter, one tested positive both for ISH and ACE-2 on immunohistochemistry while another one tested positive for nucleocapsid protein. Twelve patients showed positivity only for nucleocapsid protein on immunohistochemistry.
CONCLUSIONS CONCLUSIONS
SARS-CoV-2 was detected only in 38% of patients, without any association with a specific cutaneous phenotype, suggesting that the pathophysiology of cutaneous lesions mostly depends on the activation of the immune system. The combination of spike and nucleocapsid immunohistochemistry has higher diagnostic yield than dPCR. Skin persistence of SARS-CoV-2 may depend on timing of skin lesions, viral load, and immune response.

Identifiants

pubmed: 37075721
pii: 000530746
doi: 10.1159/000530746
doi:

Substances chimiques

RNA, Viral 0
Nucleocapsid Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

584-591

Informations de copyright

© 2023 S. Karger AG, Basel.

Auteurs

Angelo V Marzano (AV)

Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy.

Chiara Moltrasio (C)

Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Giovanni Genovese (G)

Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Marco De Andrea (M)

Department of Public Health and Pediatrics, University of Turin, Medical School, Turin, Italy.
CAAD Center for Translational Research on Autoimmune and Allergic Disease, Novara Medical School, Novara, Italy.

Valeria Caneparo (V)

CAAD Center for Translational Research on Autoimmune and Allergic Disease, Novara Medical School, Novara, Italy.

Pamela Vezzoli (P)

Dermatology Unit ASST, Papa Giovanni XXIII Hospital, Bergamo, Italy.

Denise Morotti (D)

Pathology Unit and Medical Genetics Laboratory, ASST Papa Giovanni XXIII, Bergamo, Italy.

Paolo Sena (P)

Dermatology Unit ASST, Papa Giovanni XXIII Hospital, Bergamo, Italy.

Marina Venturini (M)

Dermatology Department, ASST Spedali Civili di Brescia, University of Brescia, Brescia, Italy.

Simonetta Battocchio (S)

Unit of Pathology, ASST Spedali Civili di Brescia, Brescia, Italy.

Valentina Caputo (V)

Unit of Pathology, Grande Ospedale Metropolitano Niguarda, Milan, Italy.

Nathalie Rizzo (N)

Department of Pathology, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Carlo Alberto Maronese (CA)

Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy.

Luigia Venegoni (L)

Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy.

Francesca Laura Boggio (FL)

Division of Pathology, Università degli Studi di Milano, Foundation IRCCS, Cà Granda Ospedale Maggiore Policlinico, Milan, Italy.

Franco Rongioletti (F)

Department of Medical Sciences and Public Health, Dermatology Clinic, University of Cagliari, Cagliari, Italy.
Vita-Salute University and Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) San Raffaele, Milan, Italy.

Piergiacomo Calzavara-Pinton (P)

Dermatology Department, ASST Spedali Civili di Brescia, University of Brescia, Brescia, Italy.

Emilio Berti (E)

Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy.

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Classifications MeSH