Spesolimab,一流的抗 IL-36R 抗体:从实验室到临床

IF 2.9 3区 医学 Q2 DERMATOLOGY
Akimichi Morita, Yukari Okubo, Shinichi Imafuku, Tadashi Terui
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引用次数: 0

摘要

由多种促炎细胞因子驱动的炎症性疾病导致了针对不同疾病的靶向疗法的开发。白细胞介素(IL)-36 细胞因子与多种炎症性疾病有关。在这篇综述中,我们将介绍有关 IL-36 受体(IL-36R)靶向抗体斯贝单抗用于 IL-36 介导的皮肤病的科学证据:泛发性脓疱型银屑病(GPP)、掌跖脓疱病(PPP)、化脓性湿疹和奈瑟顿综合征(NS)。Spesolimab是一种高亲和性、特异性、人源化、拮抗性免疫球蛋白G1抗体,靶向IL-36R的结合位点与其激动剂IL-36α/β/γ和至少一种内源性拮抗剂IL-36R拮抗剂不同。spesolimab的体外和体内数据显示,它能有效抑制IL-36R介导的信号通路,在健康志愿者中进行的六项I期研究显示了良好的安全性和药代动力学(PK)特征,从而促成了一项临床试验计划的开发,以评估spesolimab治疗IL-36R介导的疾病的效果。六项研究(包括一项扩大准入计划)评估了斯派索利单抗在GPP复发患者中的疗效、安全性、PK和药物基因组学。斯派索利单抗治疗GPP复发可快速、持续地改善脓疱和皮肤的清除率,并显著改善患者报告的症状和生活质量。斯派索利单抗还能大大降低GPP复发和发作的风险,防止疾病恶化,并且具有良好的安全性。目前已进行了三项斯派索利单抗治疗 PPP 的试验;还需要进一步评估,以更好地确定哪些患者可能从治疗中获益。斯派索利单抗治疗 NS 的试验正在进行中,而其他斯派索利单抗试验表明,IL-36 在特应性皮炎的发病机制中可能只起次要作用。总之,对斯来索利单抗的研究为了解 IL-36 在人体免疫系统中的作用以及 IL-36 介导的炎症性疾病背后的机制提供了亟需的线索。Spesolimab为GPP这种医疗需求尚未得到满足的疾病提供了一种有效的靶向治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spesolimab, the first-in-class anti-IL-36R antibody: From bench to clinic

Spesolimab, the first-in-class anti-IL-36R antibody: From bench to clinic

Inflammatory diseases that are driven by several pro-inflammatory cytokines has resulted in in the development of targeted therapies across different disease settings. Interleukin (IL)-36 cytokines have been implicated in several inflammatory diseases. In this review we describe the scientific evidence surrounding the use of the IL-36 receptor (IL-36R)-targeting antibody, spesolimab, in IL-36-mediated skin diseases: generalized pustular psoriasis (GPP), palmoplantar pustulosis (PPP), hidradenitis suppurativa, and Netherton syndrome (NS). Spesolimab, a high affinity, specific, humanized, antagonistic immunoglobulin G1 antibody, targets the IL-36R at a binding site distinct from its agonists, IL-36α/β/γ, and at least one endogenous antagonist, IL-36R antagonist. In vitro and in vivo data for spesolimab show effective inhibition of IL-36R-mediated signaling pathways, and six Phase I studies in healthy volunteers presented a favorable safety and pharmacokinetic (PK) profile, leading to the development of a clinical trial program to evaluate spesolimab in the treatment of IL-36R-mediated diseases. Six studies (including an expanded access program) have evaluated the efficacy, safety, PKs, and pharmacogenomics of spesolimab in patients with GPP flares. Spesolimab treatment of GPP flares resulted in rapid and sustained improvements in pustular and skin clearance, and clinically significant improvements in patient-reported symptoms and quality of life. Spesolimab also significantly reduces the risk of GPP flares and flare occurrence, preventing disease worsening and has a favorable safety profile. There have been three trials of spesolimab in PPP; further evaluation is needed to better define those patients who might benefit from the treatment. A trial of spesolimab in NS is ongoing, while other spesolimab trials suggest that IL-36 may only play a secondary role in the pathogenesis of atopic dermatitis. In conclusion, research into spesolimab has provided much needed insight into the role of IL-36 in the human immune system and the mechanism behind IL-36-mediated inflammatory diseases. Spesolimab provides an efficacious targeted treatment for GPP, a disease with a high unmet medical need.

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来源期刊
Journal of Dermatology
Journal of Dermatology 医学-皮肤病学
CiteScore
4.60
自引率
9.70%
发文量
368
审稿时长
4-8 weeks
期刊介绍: The Journal of Dermatology is the official peer-reviewed publication of the Japanese Dermatological Association and the Asian Dermatological Association. The journal aims to provide a forum for the exchange of information about new and significant research in dermatology and to promote the discipline of dermatology in Japan and throughout the world. Research articles are supplemented by reviews, theoretical articles, special features, commentaries, book reviews and proceedings of workshops and conferences. Preliminary or short reports and letters to the editor of two printed pages or less will be published as soon as possible. Papers in all fields of dermatology will be considered.
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