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在斑秃小鼠模型中,单次皮下注射BMD-1141刺激毛发生长的效果与每日高剂量鲁索替尼相当。

A Single Subcutaneous Dose of BMD-1141 Stimulates Hair Regrowth Comparable to Daily, High-Dose Ruxolitinib in a Mouse Model of Alopecia Areata.

作者信息

Gensure Robert, King Brett, Sikkink Stephen, Mardaryev Andrei, Goforth Robyn

机构信息

Dartmouth Health Children's, Lebanon, NH 03766, USA.

Independent Researcher, Fairfield, CT 06430, USA.

出版信息

Cells. 2025 Aug 14;14(16):1251. doi: 10.3390/cells14161251.

Abstract

Alopecia areata (AA) is an autoimmune disorder of hair loss resulting from a T-cell mediated attack on hair follicles. Three Janus kinase (JAK) inhibitors have been approved for the treatment of moderate-to-severe alopecia areata; however, safety concerns for immunosuppressive therapy have limited their use. We previously demonstrated that BMD-1141, consisting of parathyroid hormone (PTH) fused to a collagen-binding domain (CBD) (PTH-CBD) improved hair retention, increased anagen hair follicles counts, and reduced hair follicle dystrophy in C3H/HeJ-engrafted mice). We now compare the effects of a single subcutaneous injection of BMD-1141 with the daily, high-dose, oral administration of the JAK inhibitor ruxolitinib on anagen hair follicle counts and hair regrowth in C3H/HeJ-engrafted mice. BMD-1141-treated mice exhibited a significant increase in anagen hair follicle counts ( < 0.05) and enhanced hair regrowth compared to ruxolitinib-treated mice after 8 weeks. Hair follicles from the BMD-1141-treated mice showed increased beta-catenin, consistent with a mechanism of stimulating the anagen transition of hair follicles, and did not increase immune cell infiltration. Thus, a single subcutaneous dose of BMD-1141 stimulated hair regrowth comparable to daily ruxolitinib, apparently by stimulating the hair cycle, rather than inhibiting the autoimmune response.

摘要

斑秃(AA)是一种自身免疫性脱发疾病,由T细胞介导对毛囊的攻击所致。三种 Janus 激酶(JAK)抑制剂已被批准用于治疗中度至重度斑秃;然而,免疫抑制疗法的安全性问题限制了它们的使用。我们之前证明,由与胶原蛋白结合域(CBD)融合的甲状旁腺激素(PTH)组成的BMD-1141(PTH-CBD)可改善毛发留存,增加生长期毛囊数量,并减少C3H/HeJ移植小鼠的毛囊营养不良。我们现在比较单次皮下注射BMD-1141与每日高剂量口服JAK抑制剂鲁索替尼对C3H/HeJ移植小鼠生长期毛囊数量和毛发生长的影响。与鲁索替尼治疗的小鼠相比,BMD-1141治疗的小鼠在8周后生长期毛囊数量显著增加(<0.05),毛发生长增强。BMD-1141治疗小鼠的毛囊显示β-连环蛋白增加,这与刺激毛囊生长期转变的机制一致,且未增加免疫细胞浸润。因此,单次皮下注射BMD-1141刺激毛发生长的效果与每日使用鲁索替尼相当,显然是通过刺激毛发生长周期,而非抑制自身免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8a3/12384116/b8d6ceaf2977/cells-14-01251-g001.jpg

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