针对2型细胞因子的单克隆抗体用于重度哮喘治疗的最新进展。

Q1 Pharmacology, Toxicology and Pharmaceutics
Garry M Walsh
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引用次数: 0

摘要

严重或难治性哮喘约占哮喘患者的5%,尽管坚持高剂量吸入糖皮质激素治疗,但症状控制不理想,导致显著发病率、生活质量下降,并伴随医疗费用的增加。在症状和分子表型水平上的显著异质性是哮喘的特征,导致需要特异性靶向治疗来阻断疾病的关键途径。靶向抑制2型细胞因子IL-4、IL-5和IL-13的单克隆抗体(mAb)为基础的生物制剂已被确定为严重哮喘的有效治疗方法,在考虑哮喘表型和内型的精心选择的患者群体中可以看到显着的临床益处。进一步开发可重复和直接的歧视性生物标志物可能有助于识别那些最有可能从这些干预治疗中受益的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent developments in the use of monoclonal antibodies targeting the type 2 cytokines for severe asthma treatment.

Severe or refractory asthma is seen in approximately 5% of asthmatic subjects who have unsatisfactory symptom control despite adherence to high-dose inhaled glucocorticoid therapies resulting in significant morbidity, reduced quality of life with attendant implications for healthcare costs. Marked heterogeneity in symptoms and at the molecular phenotypic level are hallmarks of asthma resulting in the requirement of specifically targeted treatments to block the key pathways of the disease. Monoclonal antibody (mAb)-based biologics targeted at inhibition of the type 2 cytokines IL-4, IL-5 and IL-13 have become established as effective treatments for severe asthma, with significant clinical benefit seen in carefully selected patient populations that take asthma phenotypes and endotypes into account. The further development of reproducible and straightforward discriminatory biomarkers may aid identification of those patients most likely to benefit from treatment with these interventions.

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来源期刊
Advances in pharmacology
Advances in pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
9.10
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0.00%
发文量
45
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