ArticleCell reports2025
Regulatory T cells in skin utilize the Cxcr4-Cxcl12 axis to promote hair follicle regeneration.
Article in Cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
5 citing papers in PubMed.
- Regulatory T cells: From Foxp3 to tolerance-inducing therapies.The Journal of investigative dermatology · 2026Review
- Beyond immune suppression: regenerative programs in regulatory T cells.Cell insight · 2026Review
- Regulatory T cells in the skin: Origin, function, and plasticity.JID innovations : skin science from molecules to population health · 2026Review
- The Role of dWAT-Immune Crosstalk in Hair Follicle Microenvironment in Hair Regeneration.The Journal of dermatology · 2026Review
- Insights into the context-dependent immunological roles of the CXCL12-CXCR4 axis in alopecia.Frontiers in immunology · 2026Review
Corrections and comments
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Authors and funding
7 authors.
Funding
Abstract
Regulatory T cells (Tregs) play important immunosuppressive and tissue-regenerative functions in skin. A subset of Tregs localizes to hair follicles (HFs), where they promote hair growth through activation of HF stem cells. However, the mechanisms driving Treg accumulation in HFs remain to be identified. We find that Tregs utilize Cxcr4 to accumulate in HF epithelium and that its expression is partially dependent on glucocorticoid receptor signaling. Additionally, we show that Cxcl12, the main cognate ligand of Cxcr4, is enriched in keratinocytes of the upper HF and that disruption of the Cxcr4-Cxcl12 axis results in suboptimal hair growth. Finally, we demonstrate that upper HF keratinocytes in human skin express Cxcr4 ligands in a pattern similar to that in murine skin. Collectively, these results reveal an evolutionary conserved pathway of Treg trafficking within a barrier tissue that promotes hair regeneration, which may have implications for immunotherapeutic modulation of human alopecia.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.