An Overview of the Safety and Efficacy of Monoclonal Antibodies for the Chronic Obstructive Pulmonary Disease.

IF 3.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Biologics : Targets & Therapy Pub Date : 2021-08-27 eCollection Date: 2021-01-01 DOI:10.2147/BTT.S295409
Mario Cazzola, Josuel Ora, Francesco Cavalli, Paola Rogliani, Maria Gabriella Matera
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引用次数: 10

Abstract

Several mAbs have been tested or are currently under clinical evaluation for the treatment of COPD. They can be subdivided into those that aim to block specific pro-inflammatory and pro-neutrophilic cytokines and chemokines, such as TNF-α, IL-1β, CXCL8 and IL-1β, and those that act on T2-mediated inflammation, respectively, by blocking IL-5 and/or its receptor, preventing IL-4 and IL-13 signaling, affecting IL-33 pathway and blocking TSLP. None of these approaches has proved to be effective, probably because in COPD there is no dominant cytokine or chemokine and, therefore, a single mAb cannot be effective on all pathways. With a more in-depth understanding of the numerous pheno/endotypic pathways that play a role in COPD, it may eventually be possible to identify those specific patients in whom some of these cytokines or chemokines might predominate. In this case, it will be possible to implement a personalized treatment, but the use of each mAb will only be reserved for a very limited number of subjects.

单克隆抗体治疗慢性阻塞性肺疾病的安全性和有效性综述
一些单克隆抗体已经测试或目前正在临床评估中用于治疗COPD。它们可以细分为旨在阻断特定的促炎和嗜中性细胞因子和趋化因子,如TNF-α, IL-1β, CXCL8和IL-1β,以及通过阻断IL-5和/或其受体,阻止IL-4和IL-13信号传导,影响IL-33途径和阻断TSLP分别作用于t2介导的炎症。这些方法都没有被证明是有效的,可能是因为在COPD中没有显性细胞因子或趋化因子,因此单一单抗不能对所有途径有效。随着对在COPD中发挥作用的众多表型/内源性途径的更深入了解,最终可能有可能确定这些细胞因子或趋化因子可能占主导地位的特定患者。在这种情况下,可以实施个性化治疗,但每种单抗的使用将仅用于非常有限的受试者。
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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来源期刊
Biologics : Targets & Therapy
Biologics : Targets & Therapy MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
8.30
自引率
0.00%
发文量
22
审稿时长
16 weeks
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