Evidence map›Paper›PMID 41253756›Full record

ArticleNature communications2025

CFTR modulator therapy drives microbiome restructuring through improved host physiology in cystic fibrosis: the IMMProveCF phase IV trial.

Rebecca Luise Knoll, Melanie Meihua Brauny, Evelyn Robert, Louisa Cloos, Lydia Waser, Katja Hilbert, Nina Ulmer, Barlo Hillen, Till Birkner, Theda Ulrike Patricia Bartolomaeus and 7 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Review
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  3. Article
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  5. Article
  6. Article
  7. Journal of bacteriology · 2026
    Article
  8. Review
  9. Observational
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Rebecca Luise KnollChildren's Hospital, University Medical Center of the Johannes Gutenberg‑University Mainz, Mainz, Germany.ORCID http://orcid.org/0000-0002-3496-345X
Melanie Meihua BraunyInterfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.
Evelyn RobertChildren's Hospital, University Medical Center of the Johannes Gutenberg‑University Mainz, Mainz, Germany.
Louisa CloosChildren's Hospital, University Medical Center of the Johannes Gutenberg‑University Mainz, Mainz, Germany.
Lydia WaserChildren's Hospital, University Medical Center of the Johannes Gutenberg‑University Mainz, Mainz, Germany.
Katja HilbertChildren's Hospital, University Medical Center of the Johannes Gutenberg‑University Mainz, Mainz, Germany.
Nina UlmerInterfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0009-0006-3556-9645
Barlo HillenDepartment of Sports Medicine, Prevention, and Rehabilitation, Institute of Sports Science, Johannes Gutenberg‑University Mainz, Mainz, Germany.
Till BirknerCharité-Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0003-2656-2821
Theda Ulrike Patricia BartolomaeusCharité-Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Oliver NitscheChildren's Hospital, University Medical Center of the Johannes Gutenberg‑University Mainz, Mainz, Germany.
Víctor Hugo Jarquín-DíazCharité-Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0003-3758-1091
Susan LynchDivision of Gastroenterology and Benioff Center for Microbiome Medicine, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-5695-7336
Stephan GehringChildren's Hospital, University Medical Center of the Johannes Gutenberg‑University Mainz, Mainz, Germany.
Lisa MaierInterfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-6473-4762
Krystyna PoplawskaChildren's Hospital, University Medical Center of the Johannes Gutenberg‑University Mainz, Mainz, Germany. krpoplawska@icloud.com.ORCID http://orcid.org/0000-0003-4701-3784
Sofia Kirke Forslund-StartcevaCharité-Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany. sofia.forslund@mdc-berlin.de.ORCID http://orcid.org/0000-0003-4285-6993

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 551589343Deutsche Forschungsgemeinschaft (German Research Foundation) FO 1279/6-1, Project ID 431232613 - SFB 1449 (
6 · The paper itself

Abstract

Cystic fibrosis (CF) is a genetic disorder caused by mutations in the CFTR gene, leading to impaired CFTR function, mucus accumulation, chronic infections, and inflammation. The triple combination elexacaftor/tezacaftor/ivacaftor (ETI) has transformed CF treatment by restoring CFTR function. However, how ETI-induced physiological improvements affect long-standing dysbiosis and pathogen colonization across microbiome habitats remains poorly understood. In this prospective longitudinal study (DRKS00023862), we analyzed sputum, throat, and stool microbiomes of pwCF (n = 35) before and after ETI initiation, alongside healthy controls (n = 49). The primary endpoint was longitudinal change in diversity, species richness, and microbial composition in the respiratory and intestinal microbiome, profiled by 16S rRNA gene sequencing. Secondary endpoints included changes in lung function, systemic and gastrointestinal inflammation. We show how improved CFTR function and direct antibacterial effects of ETI create a niche disadvantage for Staphylococcus in the sputum microbiome. Respiratory microbiome shifts were immediate, while gut changes emerged gradually. Escherichia abundance in stool, initially elevated in pwCF, decreased post-ETI and correlated with lower fecal calprotectin. These findings demonstrate that ETI can partially reverse CF-associated dysbiosis through improved host physiology. They offer insights into host-microbiome dynamics under therapeutic modulation and emphasize the need for confounder-aware models in complex clinical populations.

Indexed as

AminophenolsBenzodioxolesCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorMicrobiotaPyrrolesQuinolonesAdolescentAdultDrug CombinationsDysbiosisFecesFemaleGastrointestinal MicrobiomeHumansIndolesAminophenolsBenzodioxolesCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorDrug CombinationselexacaftorIndolesivacaftorPyrazolesPyridinesPyrrolesPyrrolidinesQuinolonesRNA, Ribosomal, 16Stezacaftortezacaftor, ivacaftor drug combination

Identifiers

PMID41253756
PMCPMC12627475

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.