PXD071549 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Systemic effects of cystic fibrosis transmembrane conductance regulator (CFTR) modulators on the plasma and serum proteome |
| Description | Cystic fibrosis (CF), resulting from a dysfunction in the cystic fibrosis transmembrane conductance regulator (CFTR), affects multiple organs through mucus obstruction and differences in secretion. The CFTR modulator drug combination elexacaftor/tezacaftor/ivacaftor (ELX/TEZ/IVA, ETI) has markedly improved clinical symptoms, but its broader molecular and systemic effects remain to be fully elucidated. We employed mass spectrometry-based proteomics to compare the plasma and serum proteomes of person with CF (pwCF) treated with the earlier, less effective lumacaftor/ivacaftor (LUM/IVA) combination against those receiving the more potent ELX/TEZ/IVA therapy. Our analysis revealed both specific and common pharmacodynamic signatures associated with inflammation and metabolic processes under each treatment regimen. Notably, ELX/TEZ/IVA therapy exhibited more consistent alterations across pwCF that were directed towards profiles observed in healthy individuals. Furthermore, by comparing sputum and serum proteomes of ELX/TEZ/IVA treated pwCF we identified counter directional changes in the pulmonary surfactant-associated protein B, SFTPB, a potential biomarker of lung permeability, which also correlated with lung function improvements and could be validated in an independent cohort. This study provides a comprehensive resource that enhances our understanding of CFTR modulator-driven proteome alterations, offering insights to both systemic and local protein regulation in CF. Our findings indicate that ELX/TEZ/IVA promotes broader systemic health improvements, providing critical insights that could shape future therapeutic strategies in CF. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-04-14 |
| AnnouncementXML | Submission_2026-04-14_10:31:37.789.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Marieluise Kirchner |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; |
| ModificationList | acetylated residue; monohydroxylated residue; deamidated residue; iodoacetamide derivatized residue |
| Instrument | Orbitrap Astral; Q Exactive HF-X |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2025-12-03 16:19:43 | ID requested | |
| ⏵ 1 | 2026-04-14 10:31:38 | announced | |
Publication List
| 10.1016/j.cels.2026.101569; |
| Fentker K, Kirchner M, Ziehm M, Niquet S, Popp O, Duerr J, Schaupp L, Roehmel J, Thee S, H, ä, mmerling S, Sommerburg O, Stahl M, Graeber SY, Mall MA, Mertins P, Systemic effects of cystic fibrosis transmembrane conductance regulator modulators on the plasma and serum proteome. Cell Syst, 17(5):101569(2026) [pubmed] |
Keyword List
| submitter keyword: Serum, Cystic fibrosis, ELX/TEZ/IVA, Plasma,Astral, DDA, CFTR modulator, DIA, HFX, LUM/IVA,human, Sputum, label free |
Contact List
| Philipp Mertins |
| contact affiliation | Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany. Berlin Institute of Health (BIH), Berlin, Germany. |
| contact email | Philipp.mertins@mdc-berlin.de |
| lab head | |
| Marieluise Kirchner |
| contact affiliation | Proteomics Platform, BIH@Charite |
| contact email | marieluise.kirchner@mdc-berlin.de |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD071549
- Label: PRIDE project
- Name: Systemic effects of cystic fibrosis transmembrane conductance regulator (CFTR) modulators on the plasma and serum proteome