Frontal Fibrosing Alopecia Scalp Profiling Links Th1/Th2 And JAK3 Activation With Fibrosis And Loss Of Follicular Stem Cells

    Ester Del Duca, Tae Won Song, R.D. Sanyal, Ana B. Pavel, Jesús Gay-Mimbrera, Juan Luís Sanz-Cabanillas, R. Li, J.G. Krueger, J. Ruano Ruiz, Emma Guttman‐Yassky
    TLDR Targeting immune pathways like JAK/STAT may help treat frontal fibrosing alopecia.
    The study investigated frontal fibrosing alopecia (FFA), a subtype of alopecia, by comparing scalp biopsies from FFA patients (n=12), alopecia areata (AA) patients (n=10), and controls (n=3). It found increased CD8+ T cells and CD11c+ dendritic cells in FFA and AA, with higher granzyme B mRNA in FFA. Infiltrates were located at the bulge in FFA and at the bulb in AA. Th1, Th2, and JAK-STAT signaling were up-regulated in FFA, along with markers of fibrosis and epithelial-mesenchymal transition. Hair keratin genes were downregulated in AA but not FFA. Stem cell markers CD200 and K15 were reduced in both FFA and AA, with K15 protein expression specifically diminished in FFA. The findings suggested that immune-mediated follicular damage and fibrosis in FFA could potentially be mitigated by targeting immune pathways like JAK/STAT.
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