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We are analyzing https://link.springer.com/article/10.1007/s00403-024-02899-0.

Title:
Cutaneous inflammasome driving ASC / gasdermin-D activation and IL-1β-secreting macrophages in severe atopic dermatitis | Archives of Dermatological Research
Description:
Atopic dermatitis (AD) is an inflammatory skin disease with intense pruritus, and chronic skin colonization by Staphylococcus aureus. To understand the inflammatory status in AD, we investigated the inflammasome complex, that activates ASC (Apoptosis-associated speck-like protein containing a CARD), caspase-1 and GSDMD (gasdermin-D), and production of IL-1β and IL-18. We aimed to evaluate the expression of the inflammasome pathway in the skin of adults with AD. Thirty patients with moderate to severe AD and 20 healthy controls were enrolled in the study. We performed the analysis of the inflammasome components NLRP1, NLRP3, AIM-2, IL-1β, IL-18, Caspase-1, ASC, GSDMD, and CD68 expression (macrophage marker) by immunohistochemistry and immunofluorescence. The main findings included increased expression of NLRP3, NLRP1 and AIM-2 at dermal level of severe AD; augmented IL-18 and IL-1β expression at epidermis of moderate and severe patients, and in the dermis of severe AD; augmented expression of ASC, caspase-1 and GSDMD in both epidermis and dermis of moderate and severe AD. We detected positive correlation between caspase-1, GSDMD and IL-1β (epidermis) and caspase-1 (dermis) and AD severity; NLRP3, AIM-2 and IL-1β, and NLRP3 with IL-18 in the epidermis; ASC, GSDMD and IL-1β, and NLRP3, AIM-2, caspase-1, and IL-18 in the dermis. We also evidenced the presence of CD68+ macrophages secreting GSDMD, ASC and IL-1β in moderate and severe AD. Cutaneous macrophages, early detected in moderate AD, have its role in the disease inflammatory mechanisms. Our study indicates a canonical activation pathway of inflammasomes, reinforced by the chronic status of inflammation in AD. The analysis of the inflammasome complex evidenced an imbalance in its regulation, with increased expression of the evaluated components, which is remarkably in severe AD, emphasizing its relevance as potential disease biomarkers and targets for immunomodulatory interventions.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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  • Education
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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {🔍}

article, paulo, inflammasome, severe, atopic, dermatitis, ilβ, nlrp, sao, asc, gsdmd, research, orfali, caspase, expression, study, pubmed, author, privacy, cookies, aoki, raquel, leão, skin, moderate, dermatology, brazil, supplementary, material, content, analysis, data, information, publish, search, gasdermind, macrophages, sato, aim, epidermis, dermis, access, cas, google, scholar, são, springer, log, journal, cutaneous,

Topics {✒️}

mírian nacagami sotto month download article/chapter raquel leão orfali joyce tiyeko kawakami dermatological research aims electronic supplementary material il-1β-secreting macrophages severe atopic dermatitis privacy choices/manage cookies full article pdf inflammatory skin disease chronic skin colonization atopic dermatitis sao paulo school inflammasome components nlrp1 inflammasome complex evidenced sao paulo-sp article ramos european economic area potential disease biomarkers key transcription factor promising therapeutic approach additional information publisher conditions privacy policy disease inflammatory mechanisms detected positive correlation cutaneous macrophages naiura vieira pereira ethics declarations conflict il-1β expression sato mn accepting optional cookies article archives macrophage marker staphylococcus aureus enterotoxins author correspondence personal data ethics statement inflammasome complex inflammasome pathway journal finder publish canonical activation pathway article log data protection check access instant access article number 156 gasdermin pores sao paulo são paulo

Schema {🗺️}

WebPage:
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         headline:Cutaneous inflammasome driving ASC / gasdermin-D activation and IL-1β-secreting macrophages in severe atopic dermatitis
         description: Atopic dermatitis (AD) is an inflammatory skin disease with intense pruritus, and chronic skin colonization by Staphylococcus aureus. To understand the inflammatory status in AD, we investigated the inflammasome complex, that activates ASC (Apoptosis-associated speck-like protein containing a CARD), caspase-1 and GSDMD (gasdermin-D), and production of IL-1β and IL-18. We aimed to evaluate the expression of the inflammasome pathway in the skin of adults with AD. Thirty patients with moderate to severe AD and 20 healthy controls were enrolled in the study. We performed the analysis of the inflammasome components NLRP1, NLRP3, AIM-2, IL-1β, IL-18, Caspase-1, ASC, GSDMD, and CD68 expression (macrophage marker) by immunohistochemistry and immunofluorescence. The main findings included increased expression of NLRP3, NLRP1 and AIM-2 at dermal level of severe AD; augmented IL-18 and IL-1β expression at epidermis of moderate and severe patients, and in the dermis of severe AD; augmented expression of ASC, caspase-1 and GSDMD in both epidermis and dermis of moderate and severe AD. We detected positive correlation between caspase-1, GSDMD and IL-1β (epidermis) and caspase-1 (dermis) and AD severity; NLRP3, AIM-2 and IL-1β, and NLRP3 with IL-18 in the epidermis; ASC, GSDMD and IL-1β, and NLRP3, AIM-2, caspase-1, and IL-18 in the dermis. We also evidenced the presence of CD68+ macrophages secreting GSDMD, ASC and IL-1β in moderate and severe AD. Cutaneous macrophages, early detected in moderate AD, have its role in the disease inflammatory mechanisms. Our study indicates a canonical activation pathway of inflammasomes, reinforced by the chronic status of inflammation in AD. The analysis of the inflammasome complex evidenced an imbalance in its regulation, with increased expression of the evaluated components, which is remarkably in severe AD, emphasizing its relevance as potential disease biomarkers and targets for immunomodulatory interventions.
         datePublished:2024-05-11T00:00:00Z
         dateModified:2024-05-11T00:00:00Z
         pageStart:1
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         sameAs:https://doi.org/10.1007/s00403-024-02899-0
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            Atopic dermatitis
            Inflammasome
            Keratinocytes
            Macrophage
            IL-1β
            gasdermin-D
            Dermatology
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                     address:
                        name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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                        name:Department of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
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                     name:Universidade de Sao Paulo
                     address:
                        name:Laboratory of Heart Pathology, Heart Institute (InCor), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
                        type:PostalAddress
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               name:Luiz Fernando Ferraz da Silva
               url:http://orcid.org/0000-0002-0181-6357
               affiliation:
                     name:Universidade de Sao Paulo
                     address:
                        name:Department of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
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               name:Maria Notomi Sato
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                     name:Universidade de Sao Paulo
                     address:
                        name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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               name:Raquel Leão Orfali
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                     address:
                        name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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      headline:Cutaneous inflammasome driving ASC / gasdermin-D activation and IL-1β-secreting macrophages in severe atopic dermatitis
      description: Atopic dermatitis (AD) is an inflammatory skin disease with intense pruritus, and chronic skin colonization by Staphylococcus aureus. To understand the inflammatory status in AD, we investigated the inflammasome complex, that activates ASC (Apoptosis-associated speck-like protein containing a CARD), caspase-1 and GSDMD (gasdermin-D), and production of IL-1β and IL-18. We aimed to evaluate the expression of the inflammasome pathway in the skin of adults with AD. Thirty patients with moderate to severe AD and 20 healthy controls were enrolled in the study. We performed the analysis of the inflammasome components NLRP1, NLRP3, AIM-2, IL-1β, IL-18, Caspase-1, ASC, GSDMD, and CD68 expression (macrophage marker) by immunohistochemistry and immunofluorescence. The main findings included increased expression of NLRP3, NLRP1 and AIM-2 at dermal level of severe AD; augmented IL-18 and IL-1β expression at epidermis of moderate and severe patients, and in the dermis of severe AD; augmented expression of ASC, caspase-1 and GSDMD in both epidermis and dermis of moderate and severe AD. We detected positive correlation between caspase-1, GSDMD and IL-1β (epidermis) and caspase-1 (dermis) and AD severity; NLRP3, AIM-2 and IL-1β, and NLRP3 with IL-18 in the epidermis; ASC, GSDMD and IL-1β, and NLRP3, AIM-2, caspase-1, and IL-18 in the dermis. We also evidenced the presence of CD68+ macrophages secreting GSDMD, ASC and IL-1β in moderate and severe AD. Cutaneous macrophages, early detected in moderate AD, have its role in the disease inflammatory mechanisms. Our study indicates a canonical activation pathway of inflammasomes, reinforced by the chronic status of inflammation in AD. The analysis of the inflammasome complex evidenced an imbalance in its regulation, with increased expression of the evaluated components, which is remarkably in severe AD, emphasizing its relevance as potential disease biomarkers and targets for immunomodulatory interventions.
      datePublished:2024-05-11T00:00:00Z
      dateModified:2024-05-11T00:00:00Z
      pageStart:1
      pageEnd:5
      sameAs:https://doi.org/10.1007/s00403-024-02899-0
      keywords:
         Atopic dermatitis
         Inflammasome
         Keratinocytes
         Macrophage
         IL-1β
         gasdermin-D
         Dermatology
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            name:Yasmim Álefe Leuzzi Ramos
            url:http://orcid.org/0009-0005-7185-4569
            affiliation:
                  name:Universidade de Sao Paulo
                  address:
                     name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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                  address:
                     name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
                     type:PostalAddress
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            type:Person
            name:Valeria Aoki
            url:http://orcid.org/0000-0003-4256-4413
            affiliation:
                  name:Universidade de Sao Paulo
                  address:
                     name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Mírian Nacagami Sotto
            url:http://orcid.org/0000-0001-6380-7192
            affiliation:
                  name:Universidade de Sao Paulo
                  address:
                     name:Department of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Joyce Tiyeko Kawakami
            url:http://orcid.org/0009-0007-2366-1740
            affiliation:
                  name:Universidade de Sao Paulo
                  address:
                     name:Laboratory of Heart Pathology, Heart Institute (InCor), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Luiz Fernando Ferraz da Silva
            url:http://orcid.org/0000-0002-0181-6357
            affiliation:
                  name:Universidade de Sao Paulo
                  address:
                     name:Department of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Maria Notomi Sato
            url:http://orcid.org/0000-0002-7911-1824
            affiliation:
                  name:Universidade de Sao Paulo
                  address:
                     name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
                     type:PostalAddress
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            type:Person
            name:Raquel Leão Orfali
            url:http://orcid.org/0000-0002-2807-1404
            affiliation:
                  name:Universidade de Sao Paulo
                  address:
                     name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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         name:Laboratory of Heart Pathology, Heart Institute (InCor), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
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            name:Universidade de Sao Paulo
            address:
               name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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            address:
               name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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            address:
               name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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      name:Mírian Nacagami Sotto
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            address:
               name:Department of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
               type:PostalAddress
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      name:Joyce Tiyeko Kawakami
      url:http://orcid.org/0009-0007-2366-1740
      affiliation:
            name:Universidade de Sao Paulo
            address:
               name:Laboratory of Heart Pathology, Heart Institute (InCor), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
               type:PostalAddress
            type:Organization
      name:Luiz Fernando Ferraz da Silva
      url:http://orcid.org/0000-0002-0181-6357
      affiliation:
            name:Universidade de Sao Paulo
            address:
               name:Department of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
               type:PostalAddress
            type:Organization
      name:Maria Notomi Sato
      url:http://orcid.org/0000-0002-7911-1824
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            name:Universidade de Sao Paulo
            address:
               name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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      name:Raquel Leão Orfali
      url:http://orcid.org/0000-0002-2807-1404
      affiliation:
            name:Universidade de Sao Paulo
            address:
               name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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      name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
      name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
      name:Department of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
      name:Laboratory of Heart Pathology, Heart Institute (InCor), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
      name:Department of Pathology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil
      name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
      name:Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies (LIM-56), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sala, Sao Paulo-SP, Cerqueira Cesar, Brazil
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Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

3.78s.