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Published on: April 6, 2022
Ultraviolet A light effectively reduces bacteria and viruses including coronavirus
Ali Rezaie1, Gabriela G S Leite1, Gil Y Melmed2
1Medically Associated Science and Technology (MAST) Program, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Ultraviolet-A (UVA) phototherapy shows promise for treating internal infections by reducing various pathogens, including coronavirus-229E. Studies indicate UVA is safe for internal use in mice and human cells, warranting clinical trials.
Area of Science:
- Microbiology
- Photomedicine
- Infectious Diseases
Background:
- Emerging antimicrobial-resistant and novel pathogens necessitate new therapeutic strategies.
- Ultraviolet-A (UVA) phototherapy is FDA-approved for dermatological conditions but not internal applications.
- The potential of UVA for treating internal infections remains unexplored.
Purpose of the Study:
- To investigate the effects of Ultraviolet-A (UVA) on human cells and mouse colonic tissue.
- To assess the efficacy of UVA against a range of bacteria, yeast, and viruses in vitro.
- To evaluate the safety of internal UVA exposure in a preclinical in vivo model.
Main Methods:
- Human cell lines (HeLa, alveolar, tracheal epithelial) and mouse colonic tissue were exposed to specific UVA regimens.
- Pathogen reduction was assessed for Pseudomonas aeruginosa, Klebsiella pneumoniae, Escherichia coli, Enterococcus faecalis, Clostridioides difficile, Streptococcus pyogenes, Staphylococcus epidermidis, Proteus mirabilis, and Candida albicans.
- Cell viability, oxidative DNA damage (8-Oxo-2'-deoxyguanosine), and viral protein expression were measured.
- In vivo safety was evaluated in wild-type mice using intracolonic UVA exposure, assessing endoscopic and histologic changes.
Main Results:
- Controlled UVA exposure significantly reduced all tested bacterial and yeast pathogens.
- UVA treatment of coxsackievirus-transfected HeLa cells increased cell survival.
- UVA treatment of coronavirus-229E-transfected tracheal cells reduced viral spike protein, increased antiviral signaling, and decreased cell death.
- No significant effects on human cell growth or DNA damage were observed.
- In vivo UVA exposure in mice showed no discernible adverse endoscopic, histologic, or dysplastic changes.
Conclusions:
- Specific UVA exposure conditions effectively reduce a variety of pathogens, including coronavirus-229E.
- Internal UVA application appears safe in preclinical models.
- UVA phototherapy presents a potential safe and effective treatment for internal infectious diseases.
- Further clinical studies are warranted to confirm safety and efficacy in humans.
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