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Updated: Sep 16, 2025

High-throughput Quantitative Real-time RT-PCR Assay for Determining Expression Profiles of Types I and III Interferon Subtypes
Published on: March 24, 2015
Type I Interferons in SARS-CoV-2 Cutaneous Infection: Is There a Role in Antiviral Defense?
Tatiana Mina Yendo1, Raquel Leão Orfali1, Naiura Vieira Pereira1
1Department of Dermatology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo 01246-903, SP, Brazil.
This study found SARS-CoV-2 in skin samples from deceased COVID-19 patients, revealing microscopic changes and altered immune responses. Type I interferon plays a role in the skin
Area of Science:
- Dermatology
- Virology
- Immunology
Background:
- Severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) primarily impacts the lungs, with limited understanding of its skin manifestations.
- The skin possesses intrinsic antiviral defense mechanisms, including Toll-like receptor (TLR) and interferon regulatory factor (IRF) pathway activation, and type I interferon (IFN) production.
Purpose of the Study:
- To investigate the presence and effects of SARS-CoV-2 in the skin of COVID-19 patients.
- To evaluate the cutaneous antiviral mechanisms and molecular responses to SARS-CoV-2 infection.
Main Methods:
- Skin samples from 35 deceased COVID-19 patients were analyzed.
- SARS-CoV-2 detection utilized transmission electron microscopy and RT-qPCR.
- Histopathology, RT-qPCR, and immunohistochemistry (IHC) assessed viral impact and molecular changes.
Main Results:
- SARS-CoV-2 was detected in skin, accompanied by microvascular thrombi, perivascular dermatitis, and eccrine gland necrosis.
- Increased TBK1 and reduced TNFα transcription were observed.
- Reduced ACE2, TLR7, and IL-6 expression, with elevated epidermal IFN-β, were noted. Dermal STING, IFN-β, and TNF-α decreased, while IL-6 increased in sweat glands.
Conclusions:
- The skin exhibits SARS-CoV-2 presence and associated histopathological changes.
- Type I interferon (IFN) is implicated in the cutaneous immune response to SARS-CoV-2, potentially modulating the skin's reaction to the virus.
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