Chair of Pharmacology, Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Chair of Respiratory Medicine, Department of Experimental Medicine, University of Rome Tor Vergata, Rome, Italy.
Drugs. 2020 Apr;80(5):449-458. doi: 10.1007/s40265-020-01273-4.
Thymic stromal lymphopoietin (TSLP) is an allarmin cytokine whose importance in human asthma has been repeatedly documented. Accordingly, targeting of TSLP and TSLP-mediated signalling is considered as an attractive therapeutic strategy to asthma. Tezepelumab, which is the first-in-class anti-TSLP monoclonal antibodies (mAb), is a fully human IgG2λ mAb that binds human TSLP, prevents interaction with its receptor and, consequently, inhibits multiple downstream inflammatory pathways. Because of the excellent results of Phase II trials, the Food and Drug Administration granted tezepelumab as a 'breakthrough' biological drug for the treatment of severe asthma. Several studies with this mAb are ongoing. CSJ117 is an Ab fragment that binds to TSLP and is delivered by inhalation but there is no published information on this biologic agent. Since new information suggests that targeting TSLP may be more likely to improve day-to-day asthma symptoms, in contrast to targeting mediators of the adaptive immune system, approaches that primarily act to ameliorate asthma exacerbations, novel approaches capable of blocking TSLP (for example, fully human single-chain fragment variables against TSLP, bifunctional drugs such as the one that combines an anti-IL-13 mAb with an anti-TSLP mAb, a fusion protein consisting of the ectodomains of TSLPR and IL-7Ra that extend into the extracellular space, also known as a TSLP-trap, fragments capable of disrupting the TSLP:TSLPR complex) are under preclinical investigation. However, some critical aspects remain to be clarified before being able to define this approach as the one that will probably better help patients suffering from severe asthma because of its holistic effects.
胸腺基质淋巴细胞生成素(TSLP)是一种警报素细胞因子,其在人类哮喘中的重要性已被反复证实。因此,靶向 TSLP 和 TSLP 介导的信号转导被认为是一种有吸引力的哮喘治疗策略。Tezepelumab 是一种首创的抗 TSLP 单克隆抗体(mAb),是一种完全人源 IgG2λ mAb,可与人类 TSLP 结合,防止其与受体相互作用,从而抑制多种下游炎症途径。由于 II 期试验的出色结果,食品和药物管理局授予 tezepelumab 作为治疗严重哮喘的“突破性”生物药物。正在进行几项使用这种 mAb 的研究。CSJ117 是一种与 TSLP 结合的 Ab 片段,通过吸入给药,但目前尚无关于这种生物制剂的信息。由于新的信息表明,与靶向适应性免疫系统的介质相比,靶向 TSLP 可能更有可能改善日常哮喘症状,因此,能够阻断 TSLP 的新方法(例如,针对 TSLP 的全人单链片段变量、双功能药物,例如将抗 IL-13 mAb 与抗 TSLP mAb 结合的药物、由 TSLPR 和 IL-7Ra 的细胞外结构域组成的融合蛋白,也称为 TSLP 陷阱,能够破坏 TSLP:TSLPR 复合物的片段)正在进行临床前研究。然而,在能够将这种方法定义为可能更好地帮助患有严重哮喘的患者的方法之前,还有一些关键方面需要澄清,因为它具有整体作用。