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  1. Artikel ; Online: Tertiary lymphoid structures sustain cutaneous B cell activity in hidradenitis suppurativa.

    Lowe, Margaret M / Cohen, Jarish N / Moss, Madison I / Clancy, Sean / Adler, James P / Yates, Ashley E / Naik, Haley B / Yadav, Rashi / Pauli, Mariela / Taylor, Ian / McKay, Austin / Harris, Hobart / Kim, Esther / Hansen, Scott L / Rosenblum, Michael D / Moreau, Joshua M

    JCI insight

    2024  Band 9, Heft 3

    Abstract: Hidradenitis suppurativa (HS) is a chronic skin condition affecting approximately 1% of the US population. HS skin lesions are highly inflammatory and characterized by a large immune infiltrate. While B cells and plasma cells comprise a major component ... ...

    Abstract Hidradenitis suppurativa (HS) is a chronic skin condition affecting approximately 1% of the US population. HS skin lesions are highly inflammatory and characterized by a large immune infiltrate. While B cells and plasma cells comprise a major component of this immune milieu, the biology and the contribution of these cells in HS pathogenesis are unclear. We aimed to investigate the dynamics and microenvironmental interactions of B cells within cutaneous HS lesions. Combining histological analysis, single-cell RNA sequencing, and spatial transcriptomics profiling of HS lesions, we defined the tissue microenvironment relative to B cell activity within this disease. Our findings identified tertiary lymphoid structures (TLSs) within HS lesions and described organized interactions among T cells, B cells, antigen-presenting cells, and skin stroma. We found evidence that B cells within HS TLSs actively underwent maturation, including participation in germinal center reactions and class switch recombination. Moreover, skin stroma and accumulating T cells were primed to support the formation of TLSs and facilitate B cell recruitment during HS. Our data definitively demonstrated the presence of TLSs in lesional HS skin and point to ongoing cutaneous B cell maturation through class switch recombination and affinity maturation during disease progression in this inflamed nonlymphoid tissue.
    Mesh-Begriff(e) Humans ; Hidradenitis Suppurativa/pathology ; Tertiary Lymphoid Structures/pathology ; Skin/pathology ; B-Lymphocytes/pathology ; T-Lymphocytes/pathology
    Sprache Englisch
    Erscheinungsdatum 2024-02-08
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 2379-3708
    ISSN (online) 2379-3708
    DOI 10.1172/jci.insight.169870
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Early-life inflammation primes a T helper 2 cell-fibroblast niche in skin.

    Boothby, Ian C / Kinet, Maxime J / Boda, Devi P / Kwan, Elaine Y / Clancy, Sean / Cohen, Jarish N / Habrylo, Ireneusz / Lowe, Margaret M / Pauli, Mariela / Yates, Ashley E / Chan, Jamie D / Harris, Hobart W / Neuhaus, Isaac M / McCalmont, Timothy H / Molofsky, Ari B / Rosenblum, Michael D

    Nature

    2021  Band 599, Heft 7886, Seite(n) 667–672

    Abstract: Inflammation early in life can prime the local immune milieu of peripheral tissues, which can cause lasting changes in immunological tone that confer disease protection or ... ...

    Abstract Inflammation early in life can prime the local immune milieu of peripheral tissues, which can cause lasting changes in immunological tone that confer disease protection or susceptibility
    Mesh-Begriff(e) Animals ; Animals, Newborn ; Cytokines/immunology ; Eosinophilia/pathology ; Fasciitis/pathology ; Fibroblasts/cytology ; Fibrosis/pathology ; Health ; Humans ; Inflammation/pathology ; Interleukin-13 Receptor alpha1 Subunit/metabolism ; Male ; Mice ; Skin/cytology ; Skin/pathology ; Stem Cell Niche ; T-Lymphocytes, Regulatory/cytology ; Th2 Cells/cytology ; Wound Healing
    Chemische Substanzen Cytokines ; Il13ra1 protein, mouse ; Interleukin-13 Receptor alpha1 Subunit
    Sprache Englisch
    Erscheinungsdatum 2021-10-27
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 120714-3
    ISSN 1476-4687 ; 0028-0836
    ISSN (online) 1476-4687
    ISSN 0028-0836
    DOI 10.1038/s41586-021-04044-7
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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