Proliferative activity of antigen-specific CD154+ T cells against bacterial and fungal respiratory pathogens in cystic fibrosis decreases after initiation of highly effective CFTR modulator therapy

Background: Together with impaired mucociliary clearance, lung disease in cystic fibrosis (CF) is driven by dysregulation of innate and adaptive immunity caused by dysfunctional CFTR (Cystic Fibrosis Transmembrane Conductance Regulator), leading to airway infection and hyperinflamma-tion. The highly...

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Main Authors: Patience N. Eschenhagen (Author), Petra Bacher (Author), Claudia Grehn (Author), Jochen G. Mainz (Author), Alexander Scheffold (Author), Carsten Schwarz (Author)
Format: Book
Published: Frontiers Media S.A., 2023-06-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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