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Cited 7 time in webofscience Cited 8 time in scopus
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The Microbiome in Systemic Sclerosis: Pathophysiology and Therapeutic Potential

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dc.contributor.authorKim, S.-
dc.contributor.authorPark, H.J.-
dc.contributor.authorLee, S.-I.-
dc.date.accessioned2023-01-05T05:40:01Z-
dc.date.available2023-01-05T05:40:01Z-
dc.date.issued2022-12-
dc.identifier.issn1661-6596-
dc.identifier.issn1422-0067-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/30031-
dc.description.abstractSystemic sclerosis (SSc), also known as scleroderma, is an autoimmune disease with unknown etiology characterized by multi-organ fibrosis. Despite substantial investigation on SSc-related cellular and molecular mechanisms, effective therapies are still lacking. The skin, lungs, and gut are the most affected organs in SSc, which act as physical barriers and constantly communicate with colonized microbiota. Recent reports have documented a unique microbiome signature, which may be the pathogenic trigger or driver of SSc. Since gut microbiota influences the efficacy and toxicity of oral drugs, evaluating drug–microbiota interactions has become an area of interest in disease treatment. The existing evidence highlights the potential of the microbial challenge as a novel therapeutic option in SSc. In this review, we have summarized the current knowledge about molecular mechanisms of SSc and highlighted the underlying role of the microbiome in SSc pathogenesis. We have also discussed the latest therapeutic interventions using microbiomes in SSc, including drug–microbiota interactions and animal disease models. This review aims to elucidate the pathophysiological connection and therapeutic potential of the microbiome in SSc. Insights into the microbiome will significantly improve our understanding of etiopathogenesis and developing therapeutics for SSc. © 2022 by the authors.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleThe Microbiome in Systemic Sclerosis: Pathophysiology and Therapeutic Potential-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/ijms232416154-
dc.identifier.scopusid2-s2.0-85144509022-
dc.identifier.wosid000901949400001-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, v.23, no.24-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.volume23-
dc.citation.number24-
dc.type.docTypeReview-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusGROWTH-FACTOR-BETA-
dc.subject.keywordPlusREGULATORY T-CELLS-
dc.subject.keywordPlusDERMAL FIBROSIS-
dc.subject.keywordPlusGUT MICROBIOTA-
dc.subject.keywordPlusSERUM-LEVELS-
dc.subject.keywordPlusMESENCHYMAL TRANSITION-
dc.subject.keywordPlusVASCULAR INVOLVEMENT-
dc.subject.keywordPlusSKIN FIBROSIS-
dc.subject.keywordPlusRECEPTOR 2-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordAuthoranimal model-
dc.subject.keywordAuthorbioavailability-
dc.subject.keywordAuthormicrobiota-
dc.subject.keywordAuthororal drugs-
dc.subject.keywordAuthorsystemic sclerosis-
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