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Cytokine/Chemokine assessment as a complementary diagnostic tool for inflammatory skin diseases.
Liu, Timothy J; Lin, Lynlee L; McMeniman, Erin; Wu, Jason; Kao, Yung-Ching; Kumari, Snehlata; Boyle, Glen M; Wells, James W; Soyer, H Peter; Gonzalez-Cruz, Jazmina L.
Afiliación
  • Liu TJ; Dermatology Research Centre, The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia.
  • Lin LL; Department of Dermatology, Princess Alexandra Hospital, Metro South Health, Brisbane, QLD, Australia.
  • McMeniman E; Dermatology Research Centre, The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia.
  • Wu J; Dermatology Research Centre, The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia.
  • Kao YC; Department of Dermatology, Princess Alexandra Hospital, Metro South Health, Brisbane, QLD, Australia.
  • Kumari S; Department of Dermatology, Princess Alexandra Hospital, Metro South Health, Brisbane, QLD, Australia.
  • Boyle GM; Dermatology Research Centre, The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia.
  • Wells JW; Dermatology Research Centre, The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia.
  • Soyer HP; Department of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
  • Gonzalez-Cruz JL; Dermatology Research Centre, The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia.
Front Immunol ; 13: 1028435, 2022.
Article en En | MEDLINE | ID: mdl-36466878
Inflammatory skin conditions are the 4th leading cause of non-fatal health burden in the general population worldwide. The diagnosis of skin lesions due to systemic drug reactions, viral or bacterial exanthems, or in patients with psoriasis, atopic dermatitis or contact dermatitis is often difficult and relies heavily upon conventional histopathologic examination. Conversely, it is widely accepted that the cutaneous profile of inflammatory markers, or 'inflammatory signature', is differentially expressed in various skin conditions. In this pilot study, we investigated the possibility of inflammatory skin disease diagnosis from an immunological perspective in small punch biopsies. We collected lesional and perilesional punch biopsies from 139 patients suffering from a variety of inflammatory skin conditions and attending the Dermatology Department at the Princess Alexandra Hospital in Brisbane, Australia. Using bead-based immunoassays we were able to measure 13 out of 17 inflammatory markers from a pre-selected multi-analyte panel and to detect significant differences between lesional and perilesional biopsies from each individual patient. Hierarchical and unbiased clustering methods based on inflammatory signatures grouped psoriasis and atopic dermatitis lesions into individual clusters in contrast to other skin conditions, highlighting the potential of inflammatory signatures to be used as diagnostic differentiators and to inform alternative targets in anti-inflammatory treatment strategies.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Psoriasis / Dermatitis Atópica Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Front Immunol Año: 2022 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Psoriasis / Dermatitis Atópica Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Front Immunol Año: 2022 Tipo del documento: Article País de afiliación: Australia