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dc.contributor.authorTanaka, Masamitsu
dc.contributor.authorMroz, Pawel
dc.contributor.authorDai, Tianhong
dc.contributor.authorHuang, Liyi
dc.contributor.authorMorimoto, Yuji
dc.contributor.authorKinoshita, Manabu
dc.contributor.authorYoshihara, Yasuo
dc.contributor.authorNemoto, Koichi
dc.contributor.authorShinomiya, Nariyoshi
dc.contributor.authorSeki, Suhji
dc.contributor.authorHamblin, Michael R.
dc.date.accessioned2012-08-28T19:09:23Z
dc.date.available2012-08-28T19:09:23Z
dc.date.issued2012-06
dc.date.submitted2012-05
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/72385
dc.description.abstractBackground: Local microbial infections induced by multiple-drug-resistant bacteria in the orthopedic field can be intractable, therefore development of new therapeutic modalities is needed. Photodynamic therapy (PDT) is a promising alternative modality to antibiotics for intractable microbial infections, and we recently reported that PDT has the potential to accumulate neutrophils into the infected site which leads to resolution of the infection. PDT for cancer has long been known to be able to stimulate the innate and adaptive arms of the immune system. Methodology/Principal Findings: In the present study, a murine methicillin-resistant Staphylococcus aureus (MRSA) arthritis model using bioluminescent MRSA and polystyrene microparticles was established, and both the therapeutic (Th-PDT) and preventive (Pre-PDT) effects of PDT using methylene blue as photosensitizer were examined. Although Th-PDT could not demonstrate direct bacterial killing, neutrophils were accumulated into the infectious joint space after PDT and MRSA arthritis was reduced. With the preconditioning Pre-PDT regimen, neutrophils were quickly accumulated into the joint immediately after bacterial inoculation and bacterial growth was suppressed and the establishment of infection was inhibited. Conclusions/Significance: This is the first demonstration of a protective innate immune response against a bacterial pathogen produced by PDT.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant number R01AI050875)en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0039823en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/en_US
dc.sourcePLoSen_US
dc.titlePhotodynamic Therapy Can Induce a Protective Innate Immune Response against Murine Bacterial Arthritis via Neutrophil Accumulationen_US
dc.typeArticleen_US
dc.identifier.citationTanaka, Masamitsu et al. “Photodynamic Therapy Can Induce a Protective Innate Immune Response Against Murine Bacterial Arthritis via Neutrophil Accumulation.” Ed. Hossam M. Ashour. PLoS ONE 7.6 (2012): e39823.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.approverHamblin, Michael R.
dc.contributor.mitauthorHamblin, Michael R.
dc.relation.journalPLoS ONEen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsTanaka, Masamitsu; Mroz, Pawel; Dai, Tianhong; Huang, Liyi; Morimoto, Yuji; Kinoshita, Manabu; Yoshihara, Yasuo; Nemoto, Koichi; Shinomiya, Nariyoshi; Seki, Suhji; Hamblin, Michael R.en
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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