The hair follicle is thought to be a site of ‘immune privilege,’ or relative protection from autoimmune and inflammatory responses. In particular, the long-lived, quiescent hair follicle stem cells (HFSCs) are strikingly resistant to cytotoxic immune effectors such as T cells and natural killer (NK) cells, even in systems where these cells are artificially directed to attack HFSCs. Nonetheless, many forms of alopecia are associated with immune-mediated damage of the hair follicle epithelium, suggesting a failure of immune privilege. What precipitates the collapse of HFSC immune privilege in alopecia? In this current issue of , Strobl et al use an innovative mouse model to add to our mechanistic understanding of this disorder (Strobl et al, 2024).
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11628563 | PMC |
http://dx.doi.org/10.1038/s44321-024-00170-7 | DOI Listing |
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