Jin Su-Eon, Kim Jino, Sung Jong-Hyuk
Epi Biotech Co., Ltd., Incheon, Republic of Korea.
New Hair Plastic Surgery Clinic, Seoul, Republic of Korea.
Front Pharmacol. 2024 Aug 16;15:1434961. doi: 10.3389/fphar.2024.1434961. eCollection 2024.
Therapeutic antibodies (Abs) have been anticipated as promising alternatives to conventional treatments such as topical minoxidil and oral finasteride for androgenetic alopecia (AGA). Due to the high molecular weight of typical Abs, the half-life of subcutaneous Abs exceeds 2 weeks, allowing an administration intervals of once a month or longer. Direct injection into the areas of hair loss is also feasible, potentially enhancing treatment efficacy while minimizing systemic side effects. However, therapeutic Abs are rarely developed for AGA therapy due to the requirement to be responsiveness to androgens and to exist in the extracellular fluid or cell surface surrounding the hair follicle. In this review, we introduce recent progress of antibody therapeutics in AGA targeting the prolactin receptor, Interleukin-6 receptor, C-X-C motif chemokine ligand 12, and dickkopf 1. As therapeutic Abs for AGA are still in the early stages, targets need further validation and optimization for clinical application.
治疗性抗体(Abs)被认为是雄激素性脱发(AGA)传统治疗方法(如外用米诺地尔和口服非那雄胺)的有前景的替代方案。由于典型抗体的高分子量,皮下抗体的半衰期超过2周,允许每月或更长时间给药一次。直接注射到脱发区域也是可行的,这可能会提高治疗效果,同时将全身副作用降至最低。然而,由于需要对雄激素有反应并存在于毛囊周围的细胞外液或细胞表面,很少开发用于AGA治疗的治疗性抗体。在这篇综述中,我们介绍了针对催乳素受体、白细胞介素-6受体、C-X-C基序趋化因子配体12和Dickkopf 1的AGA抗体治疗的最新进展。由于用于AGA的治疗性抗体仍处于早期阶段,靶点需要进一步验证和优化以用于临床应用。