Literature DB >> 24685200

Future biologic therapies in asthma.

Santiago Quirce1, Irina Bobolea2, Javier Domínguez-Ortega2, Pilar Barranco2.   

Abstract

Despite the administration of appropriate treatment, a high number of patients with asthma remain uncontrolled. This suggests the need for alternative treatments that are effective, safe and selective for the established asthma phenotypes, especially in patients with uncontrolled severe asthma. The most promising options among the new asthma treatments in development are biological therapies, particularly those monoclonal antibodies directed at selective targets. It should be noted that the different drugs, and especially the new biologics, act on very specific pathogenic pathways. Therefore, determination of the individual profile of predominant pathophysiological alterations of each patient will be increasingly important for prescribing the most appropriate treatment in each case. The treatment of severe allergic asthma with anti-IgE monoclonal antibody (omalizumab) has been shown to be effective in a large number of patients, and new anti-IgE antibodies with improved pharmacodynamic properties are being investigated. Among developing therapies, biologics designed to block certain pro-inflammatory cytokines, such as IL-5 (mepolizumab) and IL-13 (lebrikizumab), have a greater chance of being used in the clinic. Perhaps blocking more than one cytokine pathway (such as IL-4 and IL-13 with dulipumab) might confer increased efficacy of treatment, along with acceptable safety. Stratification of asthma based on the predominant pathogenic mechanisms of each patient (phenoendotypes) is slowly, but probably irreversibly, emerging as a tailored medical approach to asthma, and is becoming a key factor in the development of drugs for this complex respiratory syndrome.
Copyright © 2013 SEPAR. Published by Elsevier Espana. All rights reserved.

Entities:  

Keywords:  Agentes biológicos; Anticuerpos monoclonales; Asma; Asthma; Biological agents; Monoclonal antibodies; Therapy; Tratamiento

Mesh:

Substances:

Year:  2014        PMID: 24685200     DOI: 10.1016/j.arbres.2014.02.002

Source DB:  PubMed          Journal:  Arch Bronconeumol        ISSN: 0300-2896            Impact factor:   4.872


  4 in total

Review 1.  The IL-4/IL-13 axis in skin fibrosis and scarring: mechanistic concepts and therapeutic targets.

Authors:  Julie K Nguyen; Evan Austin; Alisen Huang; Andrew Mamalis; Jared Jagdeo
Journal:  Arch Dermatol Res       Date:  2019-09-06       Impact factor: 3.017

Review 2.  Prospects for Monoclonal Antibody Therapy in Pediatric Asthma.

Authors:  August Generoso; Christine Muglia-Chopra; John Oppenheimer
Journal:  Curr Allergy Asthma Rep       Date:  2018-07-10       Impact factor: 4.806

3.  Th17 Lymphocytes in Children with Asthma: Do They Influence Control?

Authors:  Verónica Moreno-Córdova; Roberto Berra-Romani; Lilian K Flores Mendoza; Julio Reyes-Leyva
Journal:  Pediatr Allergy Immunol Pulmonol       Date:  2021-12       Impact factor: 1.349

Review 4.  A review of omalizumab for the management of severe asthma.

Authors:  Ching-Hsiung Lin; Shih-Lung Cheng
Journal:  Drug Des Devel Ther       Date:  2016-07-26       Impact factor: 4.162

  4 in total

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