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Photodynamic therapy combined with antifungal drugs against chromoblastomycosis and the effect of ALA-PDT on Fonsecaea in vitro
Chromoblastomycosis is a chronic skin and subcutaneous fungal infection caused by dematiaceous fungi and is associated with low cure and high relapse rates. In southern China, Fonsecaea monophora and Fonsecaea pedrosoi are the main causative agents. We treated 5 refractory and complex cases of chrom...
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Published in: | PLoS neglected tropical diseases 2019-10, Vol.13 (10), p.e0007849-e0007849 |
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container_title | PLoS neglected tropical diseases |
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creator | Hu, Yongxuan Qi, Xinyu Sun, Hengbiao Lu, Yan Hu, Yanqing Chen, Xuyang Liu, Kangxing Yang, Yemei Mao, Zuhao Wu, Zhong Zhou, Xianyi |
description | Chromoblastomycosis is a chronic skin and subcutaneous fungal infection caused by dematiaceous fungi and is associated with low cure and high relapse rates. In southern China, Fonsecaea monophora and Fonsecaea pedrosoi are the main causative agents.
We treated 5 refractory and complex cases of chromoblastomycosis with 5-aminolevulinic acid photodynamic therapy (ALA-PDT) combined with oral antifungal drugs. The lesions improved after 4 to 9 sessions of ALA-PDT treatment at an interval of one or two weeks, and in some cases, mycological testing results became negative. The isolates were assayed for susceptibility to antifungal drugs and ALA-PDT in vitro, revealing sensitivity to terbinafine, itraconazole and voriconazole, with ALA-PDT altering the cell wall and increasing reactive oxygen species production.
These results provide the basis for the development of a new therapeutic approach, and ALA-PDT combined with oral antifungal drugs constitutes a promising alternative method for the treatment of refractory and complex cases of chromoblastomycosis. |
doi_str_mv | 10.1371/journal.pntd.0007849 |
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We treated 5 refractory and complex cases of chromoblastomycosis with 5-aminolevulinic acid photodynamic therapy (ALA-PDT) combined with oral antifungal drugs. The lesions improved after 4 to 9 sessions of ALA-PDT treatment at an interval of one or two weeks, and in some cases, mycological testing results became negative. The isolates were assayed for susceptibility to antifungal drugs and ALA-PDT in vitro, revealing sensitivity to terbinafine, itraconazole and voriconazole, with ALA-PDT altering the cell wall and increasing reactive oxygen species production.
These results provide the basis for the development of a new therapeutic approach, and ALA-PDT combined with oral antifungal drugs constitutes a promising alternative method for the treatment of refractory and complex cases of chromoblastomycosis.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0007849</identifier><identifier>PMID: 31671098</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acids ; Aminolevulinic acid ; Aminolevulinic Acid - therapeutic use ; Antifungal agents ; Antifungal Agents - therapeutic use ; Ascomycota - drug effects ; Ascomycota - radiation effects ; Biology and Life Sciences ; Cell walls ; China ; Chromoblastomycosis - drug therapy ; Chromoblastomycosis - pathology ; Chromoblastomycosis - radiotherapy ; Chromomycosis ; Chronic infection ; Combination drug therapy ; Dermatology ; Disease ; DNA, Fungal ; Drugs ; Family medical history ; Female ; Fungal infections ; Fungi ; Fungicides ; Health aspects ; Hospitals ; Humans ; Infection ; Itraconazole ; Itraconazole - therapeutic use ; Lesions ; Male ; Medicine and Health Sciences ; Microbial Sensitivity Tests ; Middle Aged ; Mycoses ; Pathogens ; Photochemotherapy ; Photochemotherapy - methods ; Photodynamic therapy ; Physical Sciences ; Reactive oxygen species ; Skin ; Skin - metabolism ; Terbinafine ; Terbinafine - therapeutic use ; Therapy ; Tropical diseases ; Voriconazole ; Voriconazole - therapeutic use</subject><ispartof>PLoS neglected tropical diseases, 2019-10, Vol.13 (10), p.e0007849-e0007849</ispartof><rights>COPYRIGHT 2019 Public Library of Science</rights><rights>2019 Hu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 Hu et al 2019 Hu et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c624t-e0940ac9ddfd5e708aa2257d362b676eed1a202f4b174f6990c60490826cb4ac3</citedby><cites>FETCH-LOGICAL-c624t-e0940ac9ddfd5e708aa2257d362b676eed1a202f4b174f6990c60490826cb4ac3</cites><orcidid>0000-0001-7286-7584 ; 0000-0002-1578-1749</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2314542035/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2314542035?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31671098$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Reynolds, Todd B.</contributor><creatorcontrib>Hu, Yongxuan</creatorcontrib><creatorcontrib>Qi, Xinyu</creatorcontrib><creatorcontrib>Sun, Hengbiao</creatorcontrib><creatorcontrib>Lu, Yan</creatorcontrib><creatorcontrib>Hu, Yanqing</creatorcontrib><creatorcontrib>Chen, Xuyang</creatorcontrib><creatorcontrib>Liu, Kangxing</creatorcontrib><creatorcontrib>Yang, Yemei</creatorcontrib><creatorcontrib>Mao, Zuhao</creatorcontrib><creatorcontrib>Wu, Zhong</creatorcontrib><creatorcontrib>Zhou, Xianyi</creatorcontrib><title>Photodynamic therapy combined with antifungal drugs against chromoblastomycosis and the effect of ALA-PDT on Fonsecaea in vitro</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><description>Chromoblastomycosis is a chronic skin and subcutaneous fungal infection caused by dematiaceous fungi and is associated with low cure and high relapse rates. In southern China, Fonsecaea monophora and Fonsecaea pedrosoi are the main causative agents.
We treated 5 refractory and complex cases of chromoblastomycosis with 5-aminolevulinic acid photodynamic therapy (ALA-PDT) combined with oral antifungal drugs. The lesions improved after 4 to 9 sessions of ALA-PDT treatment at an interval of one or two weeks, and in some cases, mycological testing results became negative. The isolates were assayed for susceptibility to antifungal drugs and ALA-PDT in vitro, revealing sensitivity to terbinafine, itraconazole and voriconazole, with ALA-PDT altering the cell wall and increasing reactive oxygen species production.
These results provide the basis for the development of a new therapeutic approach, and ALA-PDT combined with oral antifungal drugs constitutes a promising alternative method for the treatment of refractory and complex cases of chromoblastomycosis.</description><subject>Acids</subject><subject>Aminolevulinic acid</subject><subject>Aminolevulinic Acid - therapeutic use</subject><subject>Antifungal agents</subject><subject>Antifungal Agents - therapeutic use</subject><subject>Ascomycota - drug effects</subject><subject>Ascomycota - radiation effects</subject><subject>Biology and Life Sciences</subject><subject>Cell walls</subject><subject>China</subject><subject>Chromoblastomycosis - drug therapy</subject><subject>Chromoblastomycosis - pathology</subject><subject>Chromoblastomycosis - radiotherapy</subject><subject>Chromomycosis</subject><subject>Chronic infection</subject><subject>Combination drug therapy</subject><subject>Dermatology</subject><subject>Disease</subject><subject>DNA, Fungal</subject><subject>Drugs</subject><subject>Family medical history</subject><subject>Female</subject><subject>Fungal infections</subject><subject>Fungi</subject><subject>Fungicides</subject><subject>Health aspects</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Infection</subject><subject>Itraconazole</subject><subject>Itraconazole - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS neglected tropical diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Yongxuan</au><au>Qi, Xinyu</au><au>Sun, Hengbiao</au><au>Lu, Yan</au><au>Hu, Yanqing</au><au>Chen, Xuyang</au><au>Liu, Kangxing</au><au>Yang, Yemei</au><au>Mao, Zuhao</au><au>Wu, Zhong</au><au>Zhou, Xianyi</au><au>Reynolds, Todd B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photodynamic therapy combined with antifungal drugs against chromoblastomycosis and the effect of ALA-PDT on Fonsecaea in vitro</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2019-10-01</date><risdate>2019</risdate><volume>13</volume><issue>10</issue><spage>e0007849</spage><epage>e0007849</epage><pages>e0007849-e0007849</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>Chromoblastomycosis is a chronic skin and subcutaneous fungal infection caused by dematiaceous fungi and is associated with low cure and high relapse rates. In southern China, Fonsecaea monophora and Fonsecaea pedrosoi are the main causative agents.
We treated 5 refractory and complex cases of chromoblastomycosis with 5-aminolevulinic acid photodynamic therapy (ALA-PDT) combined with oral antifungal drugs. The lesions improved after 4 to 9 sessions of ALA-PDT treatment at an interval of one or two weeks, and in some cases, mycological testing results became negative. The isolates were assayed for susceptibility to antifungal drugs and ALA-PDT in vitro, revealing sensitivity to terbinafine, itraconazole and voriconazole, with ALA-PDT altering the cell wall and increasing reactive oxygen species production.
These results provide the basis for the development of a new therapeutic approach, and ALA-PDT combined with oral antifungal drugs constitutes a promising alternative method for the treatment of refractory and complex cases of chromoblastomycosis.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31671098</pmid><doi>10.1371/journal.pntd.0007849</doi><orcidid>https://orcid.org/0000-0001-7286-7584</orcidid><orcidid>https://orcid.org/0000-0002-1578-1749</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acids Aminolevulinic acid Aminolevulinic Acid - therapeutic use Antifungal agents Antifungal Agents - therapeutic use Ascomycota - drug effects Ascomycota - radiation effects Biology and Life Sciences Cell walls China Chromoblastomycosis - drug therapy Chromoblastomycosis - pathology Chromoblastomycosis - radiotherapy Chromomycosis Chronic infection Combination drug therapy Dermatology Disease DNA, Fungal Drugs Family medical history Female Fungal infections Fungi Fungicides Health aspects Hospitals Humans Infection Itraconazole Itraconazole - therapeutic use Lesions Male Medicine and Health Sciences Microbial Sensitivity Tests Middle Aged Mycoses Pathogens Photochemotherapy Photochemotherapy - methods Photodynamic therapy Physical Sciences Reactive oxygen species Skin Skin - metabolism Terbinafine Terbinafine - therapeutic use Therapy Tropical diseases Voriconazole Voriconazole - therapeutic use |
title | Photodynamic therapy combined with antifungal drugs against chromoblastomycosis and the effect of ALA-PDT on Fonsecaea in vitro |
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