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Pneumonia treatment by photodynamic therapy with extracorporeal illumination ‐ an experimental model

Infectious pneumonia is a major cause of morbidity/mortality, mainly because of the increasing rate of microorganisms resistant to antibiotics. Photodynamic Therapy (PDT) is emerging as a promising approach, as effects are based on oxidative stress, preventing microorganism resistance. In two previo...

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Autores principales: Geralde, Mariana C., Leite, Ilaiáli S., Inada, Natalia M., Salina, Ana Carolina G., Medeiros, Alexandra I., Kuebler, Wolfgang M., Kurachi, Cristina, Bagnato, Vanderlei S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350187/
https://www.ncbi.nlm.nih.gov/pubmed/28292878
http://dx.doi.org/10.14814/phy2.13190
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author Geralde, Mariana C.
Leite, Ilaiáli S.
Inada, Natalia M.
Salina, Ana Carolina G.
Medeiros, Alexandra I.
Kuebler, Wolfgang M.
Kurachi, Cristina
Bagnato, Vanderlei S.
author_facet Geralde, Mariana C.
Leite, Ilaiáli S.
Inada, Natalia M.
Salina, Ana Carolina G.
Medeiros, Alexandra I.
Kuebler, Wolfgang M.
Kurachi, Cristina
Bagnato, Vanderlei S.
author_sort Geralde, Mariana C.
collection PubMed
description Infectious pneumonia is a major cause of morbidity/mortality, mainly because of the increasing rate of microorganisms resistant to antibiotics. Photodynamic Therapy (PDT) is emerging as a promising approach, as effects are based on oxidative stress, preventing microorganism resistance. In two previous studies, the in vitro inactivation of Streptococcus pneumoniae using indocyanine green (ICG) and infrared light source was a success killing 5 log(10) colony‐forming units (CFU/mL) with only 10 μmol/L ICG. In this work, a proof‐of‐principle protocol was designed to treat lung infections by PDT using extracorporeal illumination with a 780 nm laser device and also ICG as photosensitizer. Hairless mice were infected with S. pneumoniae and PDT was performed two days after infection. For control groups, CFU recovery ranged between 10(3)–10(4)/mouse. For PDT group, however, no bacteria were recovered in 80% of the animals. Based on this result, animal survival was evaluated separately over 50 days. No deaths occurred in PDT group, whereas 60% of the control group died. Our results indicate that extracorporeal PDT has the potential for pneumonia treatment, and pulmonary decontamination with PDT may be used as a single therapy or as an antibiotics adjuvant.
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spelling pubmed-53501872017-03-17 Pneumonia treatment by photodynamic therapy with extracorporeal illumination ‐ an experimental model Geralde, Mariana C. Leite, Ilaiáli S. Inada, Natalia M. Salina, Ana Carolina G. Medeiros, Alexandra I. Kuebler, Wolfgang M. Kurachi, Cristina Bagnato, Vanderlei S. Physiol Rep Original Research Infectious pneumonia is a major cause of morbidity/mortality, mainly because of the increasing rate of microorganisms resistant to antibiotics. Photodynamic Therapy (PDT) is emerging as a promising approach, as effects are based on oxidative stress, preventing microorganism resistance. In two previous studies, the in vitro inactivation of Streptococcus pneumoniae using indocyanine green (ICG) and infrared light source was a success killing 5 log(10) colony‐forming units (CFU/mL) with only 10 μmol/L ICG. In this work, a proof‐of‐principle protocol was designed to treat lung infections by PDT using extracorporeal illumination with a 780 nm laser device and also ICG as photosensitizer. Hairless mice were infected with S. pneumoniae and PDT was performed two days after infection. For control groups, CFU recovery ranged between 10(3)–10(4)/mouse. For PDT group, however, no bacteria were recovered in 80% of the animals. Based on this result, animal survival was evaluated separately over 50 days. No deaths occurred in PDT group, whereas 60% of the control group died. Our results indicate that extracorporeal PDT has the potential for pneumonia treatment, and pulmonary decontamination with PDT may be used as a single therapy or as an antibiotics adjuvant. John Wiley and Sons Inc. 2017-03-14 /pmc/articles/PMC5350187/ /pubmed/28292878 http://dx.doi.org/10.14814/phy2.13190 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Geralde, Mariana C.
Leite, Ilaiáli S.
Inada, Natalia M.
Salina, Ana Carolina G.
Medeiros, Alexandra I.
Kuebler, Wolfgang M.
Kurachi, Cristina
Bagnato, Vanderlei S.
Pneumonia treatment by photodynamic therapy with extracorporeal illumination ‐ an experimental model
title Pneumonia treatment by photodynamic therapy with extracorporeal illumination ‐ an experimental model
title_full Pneumonia treatment by photodynamic therapy with extracorporeal illumination ‐ an experimental model
title_fullStr Pneumonia treatment by photodynamic therapy with extracorporeal illumination ‐ an experimental model
title_full_unstemmed Pneumonia treatment by photodynamic therapy with extracorporeal illumination ‐ an experimental model
title_short Pneumonia treatment by photodynamic therapy with extracorporeal illumination ‐ an experimental model
title_sort pneumonia treatment by photodynamic therapy with extracorporeal illumination ‐ an experimental model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350187/
https://www.ncbi.nlm.nih.gov/pubmed/28292878
http://dx.doi.org/10.14814/phy2.13190
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