Changes in the cystic fibrosis airway microbiome in response to CFTR modulator therapy

The development of CFTR modulator therapies significantly changed the treatment scheme of people with cystic fibrosis. However, CFTR modulator therapy is still a life-long treatment, which is not able to correct the genetic defect and cure the disease. Therefore, it becomes crucial to understand the...

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Hauptverfasser: Yi, Buqing (VerfasserIn) , Dalpke, Alexander (VerfasserIn) , Boutin, Sébastien (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 17 March 2021
In: Frontiers in Cellular and Infection Microbiology
Year: 2021, Jahrgang: 11, Pages: 1-7
ISSN:2235-2988
DOI:10.3389/fcimb.2021.548613
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3389/fcimb.2021.548613
Verlag, lizenzpflichtig, Volltext: https://www.frontiersin.org/articles/10.3389/fcimb.2021.548613/full
Volltext
Verfasserangaben:Buqing Yi, Alexander H. Dalpke and Sébastien Boutin
Beschreibung
Zusammenfassung:The development of CFTR modulator therapies significantly changed the treatment scheme of people with cystic fibrosis. However, CFTR modulator therapy is still a life-long treatment, which is not able to correct the genetic defect and cure the disease. Therefore, it becomes crucial to understand the effects of such modulation of CFTR function on the airway physiology, especially on airway infections and inflammation that are currently the major life-limiting factors in people with cystic fibrosis. In this context, understanding the dynamics of airway microbiome changes in response to modulator therapy plays an essential role in developing strategies for managing airway infections. Whether and how the newly available therapies affect the airway microbiome is still at the beginning of being deciphered. We present here a brief review summarizing the latest information about microbiome alterations in light of modern cystic fibrosis modulator therapy.
Beschreibung:Gesehen am 26.05.2021
Beschreibung:Online Resource
ISSN:2235-2988
DOI:10.3389/fcimb.2021.548613