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Investigational thymic stromal lymphopoietin inhibitors for the treatment of asthma: a systematic review.

Authors :
Rogliani P
Manzetti GM
Bettin FR
D'Auria M
Calzetta L
Source :
Expert opinion on investigational drugs [Expert Opin Investig Drugs] 2024 Jan; Vol. 33 (1), pp. 39-49. Date of Electronic Publication: 2024 Feb 12.
Publication Year :
2024

Abstract

Introduction: Severe asthma patients often remain uncontrolled despite high-intensity therapies. Biological therapies targeting thymic stromal lymphopoietin (TSLP), a key player in asthma pathogenesis, have emerged as potential options. Currently, the only TSLP inhibitor approved for the treatment of severe asthma is the immunoglobulin G (IgG) 2λ anti-TSLP monoclonal antibody (mAb) tezepelumab.<br />Areas Covered: This systematic review assesses the efficacy and safety of investigational TSLP inhibitors across different stages of development for asthma treatment.<br />Expert Opinion: TSLP contributes to airway inflammation, making it a pivotal therapeutic target. Ecleralimab, an inhaled antibody fragment antigen binding, shows promising evidence in enhancing efficacy and reducing systemic adverse events. SAR443765, with its NANOBODY® formulation and bispecific inhibition of TSLP and IL-13, offers improved tissue penetration and efficacy. The mAB TQC2731 exhibits high in vitro bioactivity, and the strength of the mAb UPB-101 is to act against the TSLP receptor. Some studies include mild and moderate asthma patients, suggesting the potential for extending biological therapy to non-severe patients. This systematic review highlights the potential of TSLP inhibitors as valuable additions to asthma treatment, even in milder forms of the disease. Future research and cost-reduction efforts are needed to expanding access to these promising therapies.

Details

Language :
English
ISSN :
1744-7658
Volume :
33
Issue :
1
Database :
MEDLINE
Journal :
Expert opinion on investigational drugs
Publication Type :
Academic Journal
Accession number :
38206116
Full Text :
https://doi.org/10.1080/13543784.2024.2305144