Tezepelumab Anti-TSLP (thymic stromal lymphopoietin) Treatment of severe asthma

被引:0
|
作者
Yao, Y. [1 ]
Ali, Z. [1 ]
Thomsen, S. F. [1 ,2 ]
机构
[1] Bispebjerg Hosp, Dept Dermatovenereol & Wound Healing Ctr, Bispebjerg Bakke 23, DK-2400 Copenhagen NV, Denmark
[2] Univ Copenhagen, Dept Biomed Sci, Copenhagen, Denmark
关键词
Tezepelumab; AMG-157; MEDI-9929; TSLP; Asthma; Atopic dermatitis; Biologics; Pharmacokinetics; Clinical study; GENOME-WIDE ASSOCIATION; IGM(+) B-CELLS; UNCONTROLLED ASTHMA; IN-VITRO; PHARMACOKINETICS; DIFFERENTIATION; TOLERABILITY; PHENOTYPE; CYTOKINE; SAFETY;
D O I
10.1358/dof.2021.46.7.3301491
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Thymic stromal lymphopoietin (TSLP) is an epithelial-derived cytokine of the interleukin-2 (IL-2) cytokine family with both homeostatic and inflammatory properties in the human organism. Aberrant production of TSLP has been observed in several type 2 allergic disorders such as bronchial asthma, atopic dermatitis and allergic rhinitis, prompting the development of anti-TSLP agents. In this review, we present the current known pharmacodynamics, pharmacokinetics, efficacy, safety and ongoing trials of tezepelumab. Tezepelumab (AMG-157, MEDI-9929) is a fully human immunoglobulin G subclass 2 (lgG2)anti-TSLP monoclonal antibody under investigation for the treatment of moderate to severe asthma. A phase 11 study has concluded that subcutaneously administered tezepelumab at doses of 210 mg every 4 weeks reduces exacerbation rates of asthma other than the type 2 endotype, improves lung function in asthmatic patients, and reduces levels of biomarkers of type 2 inflammation. Tezepelumab was generally well-tolerated with an acceptable safety profile and low rate of serious adverse events and discontinuations due to adverse events.
引用
收藏
页码:529 / 536
页数:8
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