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Which Therapy for Non-Type(T)2/T2-Low Asthma
Currently, the asthmatic population is divided into Type 2-high and non-Type 2/Type 2-low asthmatics, with 50% of patients belonging to one of the two groups. Differently from T2-high, T2-low asthma has not been clearly defined yet, and the T2-low patients are identified on the basis of the absence...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779705/ https://www.ncbi.nlm.nih.gov/pubmed/35055325 http://dx.doi.org/10.3390/jpm12010010 |
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author | Ricciardolo, Fabio L. M. Carriero, Vitina Bertolini, Francesca |
author_facet | Ricciardolo, Fabio L. M. Carriero, Vitina Bertolini, Francesca |
author_sort | Ricciardolo, Fabio L. M. |
collection | PubMed |
description | Currently, the asthmatic population is divided into Type 2-high and non-Type 2/Type 2-low asthmatics, with 50% of patients belonging to one of the two groups. Differently from T2-high, T2-low asthma has not been clearly defined yet, and the T2-low patients are identified on the basis of the absence or non-predominant expression of T2-high biomarkers. The information about the molecular mechanisms underpinning T2-low asthma is scarce, but researchers have recognized as T2-low endotypes type 1 and type 3 immune response, and remodeling events occurring without inflammatory processes. In addition, the lack of agreed biomarkers reprents a challenge for the research of an effective therapy. The first-choice medication is represented by inhaled corticosteroids despite a low efficacy is reported for/in T2-low patients. However, macrolides and long-acting anti-muscarinic drugs have been recognized as efficacious. In recent years, clinical trials targeting biomarkers playing key roles in T3 and T1 immune pathways, alarmins, and molecules involved in neutrophil recruitment have provided conflicting results probably misleading (or biased) in patients’ selection. However, further studies are warranted to achieve a precise characterization of T2-low asthma with the aim of defining a tailored therapy for each single asthmatic patient. |
format | Online Article Text |
id | pubmed-8779705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87797052022-01-22 Which Therapy for Non-Type(T)2/T2-Low Asthma Ricciardolo, Fabio L. M. Carriero, Vitina Bertolini, Francesca J Pers Med Review Currently, the asthmatic population is divided into Type 2-high and non-Type 2/Type 2-low asthmatics, with 50% of patients belonging to one of the two groups. Differently from T2-high, T2-low asthma has not been clearly defined yet, and the T2-low patients are identified on the basis of the absence or non-predominant expression of T2-high biomarkers. The information about the molecular mechanisms underpinning T2-low asthma is scarce, but researchers have recognized as T2-low endotypes type 1 and type 3 immune response, and remodeling events occurring without inflammatory processes. In addition, the lack of agreed biomarkers reprents a challenge for the research of an effective therapy. The first-choice medication is represented by inhaled corticosteroids despite a low efficacy is reported for/in T2-low patients. However, macrolides and long-acting anti-muscarinic drugs have been recognized as efficacious. In recent years, clinical trials targeting biomarkers playing key roles in T3 and T1 immune pathways, alarmins, and molecules involved in neutrophil recruitment have provided conflicting results probably misleading (or biased) in patients’ selection. However, further studies are warranted to achieve a precise characterization of T2-low asthma with the aim of defining a tailored therapy for each single asthmatic patient. MDPI 2021-12-23 /pmc/articles/PMC8779705/ /pubmed/35055325 http://dx.doi.org/10.3390/jpm12010010 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Ricciardolo, Fabio L. M. Carriero, Vitina Bertolini, Francesca Which Therapy for Non-Type(T)2/T2-Low Asthma |
title | Which Therapy for Non-Type(T)2/T2-Low Asthma |
title_full | Which Therapy for Non-Type(T)2/T2-Low Asthma |
title_fullStr | Which Therapy for Non-Type(T)2/T2-Low Asthma |
title_full_unstemmed | Which Therapy for Non-Type(T)2/T2-Low Asthma |
title_short | Which Therapy for Non-Type(T)2/T2-Low Asthma |
title_sort | which therapy for non-type(t)2/t2-low asthma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779705/ https://www.ncbi.nlm.nih.gov/pubmed/35055325 http://dx.doi.org/10.3390/jpm12010010 |
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