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雄激素性脱发中抗体疗法的最新进展。

Recent approaches of antibody therapeutics in androgenetic alopecia.

作者信息

Jin Su-Eon, Kim Jino, Sung Jong-Hyuk

机构信息

Epi Biotech Co., Ltd., Incheon, Republic of Korea.

New Hair Plastic Surgery Clinic, Seoul, Republic of Korea.

出版信息

Front Pharmacol. 2024 Aug 16;15:1434961. doi: 10.3389/fphar.2024.1434961. eCollection 2024.

DOI:10.3389/fphar.2024.1434961
PMID:39221145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11362041/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f1d/11362041/83d44daaca4f/fphar-15-1434961-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f1d/11362041/a80e96dd4645/fphar-15-1434961-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f1d/11362041/83d44daaca4f/fphar-15-1434961-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f1d/11362041/a80e96dd4645/fphar-15-1434961-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f1d/11362041/83d44daaca4f/fphar-15-1434961-g002.jpg

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本文引用的文献

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Int J Mol Sci. 2024 Jan 30;25(3):1705. doi: 10.3390/ijms25031705.
2
Interplay between androgen and CXCR4 chemokine signaling in myelin repair.雄激素与 CXCR4 趋化因子信号在髓鞘修复中的相互作用。
Acta Neuropathol Commun. 2024 Jan 30;12(1):18. doi: 10.1186/s40478-024-01730-1.
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CXCR4/CXCL12 axis: "old" pathway as "novel" target for anti-inflammatory drug discovery.CXCR4/CXCL12 轴:“旧”通路作为抗炎药物发现的“新”靶点。
Med Res Rev. 2024 May;44(3):1189-1220. doi: 10.1002/med.22011. Epub 2024 Jan 4.
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Subcutaneous Administration of Monoclonal Antibodies: Pharmacology, Delivery, Immunogenicity, and Learnings From Applications to Clinical Development.单克隆抗体的皮下给药:药理学、给药方式、免疫原性及临床开发应用经验
Clin Pharmacol Ther. 2024 Mar;115(3):422-439. doi: 10.1002/cpt.3150. Epub 2024 Jan 10.
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Involvement of DKK1 secreted from adipose-derived stem cells in alopecia areata.脂肪源性干细胞分泌的 DKK1 参与斑秃的发病机制。
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Recent Development of Novel Aminoethyl-Substituted Chalcones as Potential Drug Candidates for the Treatment of Alzheimer's Disease.新型氨基乙基取代查耳酮作为治疗阿尔茨海默病潜在药物的最新研究进展。
Molecules. 2023 Sep 12;28(18):6579. doi: 10.3390/molecules28186579.
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Treatment of Androgenetic Alopecia: Current Guidance and Unmet Needs.雄激素性脱发的治疗:当前指南与未满足的需求。
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Engineering protein-based therapeutics through structural and chemical design.通过结构和化学设计工程蛋白质类治疗药物。
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