4.3 Review

Targeting TSLP in Asthma

Journal

JOURNAL OF ASTHMA AND ALLERGY
Volume 15, Issue -, Pages 749-765

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/JAA.S275039

Keywords

thymic stromal lymphopoietin; TSLP; asthma; exacerbation rates; anti-TSLP

Funding

  1. Amgen Inc.
  2. AstraZeneca

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TSLP is a cytokine involved in asthma inflammation, and its inhibitor tezepelumab is considered a novel approach for treating asthma. Recent studies have shown that tezepelumab can safely and effectively improve asthma control in patients with severe asthma, and it has positive effects on multiple asthma phenotypes.
Thymic stromal lymphopoietin (TSLP) is an epithelial cell-derived cytokine implicated in the initiation and persistence of inflammatory pathways in asthma. Released in response to a range of epithelial insults (eg, allergens, viruses, bacteria, pollutants, and smoke), TSLP initiates multiple downstream innate and adaptive immune responses involved in asthma inflammation. Inhibition of TSLP is postulated to represent a novel approach to treating the diverse phenotypes and endotypes of asthma. Tezepelumab, the TSLP inhibitor farthest along in clinical development, is a human monoclonal antibody (IgG2 lambda) that binds specifically to TSLP, preventing interactions with its heterodimeric receptor. Results of recently published phase 2 and 3 studies, reviewed in this article, provide evidence of the safety and efficacy of tezepelumab that builds on initial findings. Tezepelumab is safe, well tolerated, and provides clinically meaningful improvements in asthma control, including reduced incidence of exacerbations and hospitalizations in patients with severe asthma. Clinical benefits were associated with reductions in levels of a broad spectrum of cytokines (eg, interleukin [IL]-5, IL-13) and baseline biomarkers (eg, blood eosinophils, immunoglobulin [Ig]E, fractional exhaled nitric oxide [FeNO]) and were observed across a range of severe asthma phenotypes (ie, eosinophilic and non-eosinophilic). These data strengthen the notion that anti-TSLP elicits broad inhibitory effects on pathways that are key to asthma inflammation rather than on narrower inhibition of individual downstream factors. This review presents the rationale for targeting TSLP to treat asthma, as well as the clinical effects of TSLP blockade on asthma outcomes, biomarkers of disease activity, airway inflammation, lung physiology, and patient symptoms.

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