Senolytics: from pharmacological inhibitors to immunotherapies, a promising future for patients' treatment.

IF 4.1 Q2 GERIATRICS & GERONTOLOGY
V Lelarge, R Capelle, F Oger, T Mathieu, B Le Calvé
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Abstract

The involvement of cellular senescence in the initiation and propagation of diseases is clearly characterized, making the elimination of senescent cells essential to treat age-related diseases. The development of senolytic drugs demonstrated that targeting these cells limits the deterioration of patients' condition, by inducing apoptosis. Nevertheless, the first generations of senolytics which has been developed displayed their activities through specific mechanisms and demonstrated several limitations during clinical development. However, the rational to eliminate senescent cells remains evident, with the necessity to develop specific therapies in a context of diseases and tissues. The evolutions in the field of drug discovery open the way to a new generation of senolytic therapies, such as immunological approaches (CAR-T cells, Antibody-Drug Conjugated or vaccines), which require preliminary steps of research to identify markers specifically expressed on senescent cells, demonstrating promising specific effects. Currently, the preclinical development of these strategies appears more challenging to avoid strong side effects, but the expected results are commensurate with patients' hopes for treatments. In this review, we highlight the fact that the classical senolytic approach based on drug repurposing display limited efficacy and probably reached its limits in term of clinical development. The recent development of more complex therapies and the extension of interest in the domain of senescence in different fields of research allow to extend the possibility to discover powerful therapies. The future of age-related diseases treatment is linked to the development of new approaches based on cell therapy or immunotherapy to offer the best treatment for patients.

Abstract Image

衰老剂:从药理抑制剂到免疫疗法,患者治疗的美好未来。
细胞衰老与疾病的诱发和传播有明显的关系,因此消除衰老细胞对治疗与年龄有关的疾病至关重要。衰老分解药物的开发表明,针对这些细胞的药物可以通过诱导细胞凋亡来限制患者病情的恶化。然而,已开发出的第一代衰老溶解剂通过特定机制显示了其活性,并在临床开发过程中表现出了一些局限性。然而,消除衰老细胞的合理性仍然显而易见,有必要针对不同的疾病和组织开发特定的疗法。药物发现领域的发展为新一代的衰老疗法开辟了道路,如免疫疗法(CAR-T 细胞、抗体药物共轭或疫苗),这些疗法需要初步的研究步骤,以确定衰老细胞上特异性表达的标记物,并显示出有希望的特异性效果。目前,这些策略的临床前开发似乎更具挑战性,以避免强烈的副作用,但预期结果与患者对治疗的希望是一致的。在这篇综述中,我们强调了这样一个事实,即基于药物再利用的经典衰老溶解疗法显示出有限的疗效,在临床开发方面可能已达到极限。最近,更复杂疗法的开发以及不同研究领域对衰老领域兴趣的扩大,为发现强有力的疗法提供了可能。老年相关疾病治疗的未来与基于细胞疗法或免疫疗法的新方法的开发息息相关,以便为患者提供最佳治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
8.90
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