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AuthorZupin, Luisa
AuthorClemente, Libera
AuthorFontana, Francesco
AuthorCrovella, Sergio
Available date2023-01-10T06:02:28Z
Publication Date2022-01-01
Publication NameJournal of Biophotonics
Identifierhttp://dx.doi.org/10.1002/jbio.202200203
CitationZupin, L., Clemente, L., Fontana, F., Crovella, S., J. Biophotonics 2023, e202200203. https://doi.org/10.1002/jbio.202200203
ISSN1864063X
URIhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85145508061&origin=inward
URIhttp://hdl.handle.net/10576/38278
AbstractPhotobiomodulation therapy (PBMT) employing laser light has been emerging as a safe strategy to challenge viruses. In this study the effect of blue and near-infrared (NIR) laser light was assessed in an in vitro model of SARS-CoV-2 infection. PBMT at blue wavelength inhibited viral amplification when the virus was directly irradiated and then transferred to cell culture and when cells already infected were treated. The NIR wavelength resulted less efficacious showing a minor effect on the reduction of the viral load. The cells receiving the irradiated virus or directly irradiated rescued their viability to level comparable to not treated cells. Virion integrity and antigenicity were preserved after blue and NIR irradiation, suggesting that the PBMT antiviral effect was not correlated to viral lipidic envelope disruption. Our results suggested that PBMT can be considered a valid strategy to counteract SARS-CoV-2 infection, at least in vitro.
SponsorThis work was supported by the Ministry of Health, Rome – Italy, in collaboration with the Institute for Maternal and Child Health IRCCS Burlo Garofolo, Trieste – Italy (RC 15/2017, 47/2020). The Graphical Abstract was created with Biorender.com. Open access funding provided by BIBLIOSAN.
Languageen
PublisherWiley
Subjectantiviral
blue and near-infrared laser light
photobiomodulation therapy
SARS-CoV-2
vero E6 cells
TitleEffect of near-infrared and blue laser light on vero E6 cells SARS-CoV-2 infection model
TypeArticle
ESSN1864-0648
dc.accessType Open Access


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