Evidence map›Paper›PMID 39160214›Full record

ArticleNature communications2024

A lactobacilli-based inhaled live biotherapeutic product attenuates pulmonary neutrophilic inflammation.

Teodora Nicola, Nancy Wenger, Xin Xu, Michael Evans, Luhua Qiao, Gabriel Rezonzew, Youfeng Yang, Tamas Jilling, Camilla Margaroli, Kristopher Genschmer and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Journal of bacteriology · 2026
    Review
  2. Live AirwayEnvironment & health (Washington, D.C.) · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. The gut-lung axis in early life: microbiome-associated mechanisms and clinical relevance.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article
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

15 authors.

Teodora Nicola *Division of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
Nancy Wenger *Division of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
Xin XuDivision of Pulmonary, Allergy and Critical Care Medicine, Program in Protease and Matrix Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Michael EvansDivision of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
Luhua QiaoDivision of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
Gabriel RezonzewDivision of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
Youfeng YangDivision of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
Tamas JillingDivision of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
Camilla MargaroliDivision of Pulmonary, Allergy and Critical Care Medicine, Program in Protease and Matrix Biology, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0000-0003-3952-0778
Kristopher GenschmerDivision of Pulmonary, Allergy and Critical Care Medicine, Program in Protease and Matrix Biology, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0000-0002-1836-9522
Kent WillisDivision of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0000-0001-7338-0399
Namasivayam AmbalavananDivision of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0000-0003-0731-9092
J Edwin BlalockDivision of Pulmonary, Allergy and Critical Care Medicine, Program in Protease and Matrix Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Amit GaggarDivision of Pulmonary, Allergy and Critical Care Medicine, Program in Protease and Matrix Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Charitharth Vivek LalDivision of Neonatology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA. clal@uabmc.edu.

Funding

A Novel Exosomal Inflammatory PathwayR35HL135710 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BLALOCK, J EDWIN · 2017 to 2023
$6.8M
Pathogenic Exosomes in COPDR35HL166433 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI J Edwin Blalock · 2023 to 2026
$4.1M
An Inhaled Microbiome-Targeted Biotherapeutic for Treatment of COPDR44HL164156 · NHLBI · RESBIOTIC, INC. · PI NICOLA, TEODORA · 2023 to 2025
$2.3M
Let-7b in BPDR01HL156275 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Namasivayam Ambalavanan · 2023 to 2026
$2.2M
Mechanisms of Pulmonary Microbiota-Induced Inflammation and Vascular Dysfunction in Neonatal Lung InjuryK08HL141652 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LAL, CHARITHARTH VIVEK · 2019 to 2023
$838k
NHLBI NIH HHS K08 HL141652NHLBI NIH HHS R01 HL156275NHLBI NIH HHS R35 HL135710NHLBI NIH HHS R35 HL166433NHLBI NIH HHS R44 HL164156U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL156275U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R35HL135710U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R35HL166433U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R44HL164156
6 · The paper itself

Abstract

Bronchopulmonary dysplasia (BPD) is a chronic lung disease of prematurity. Exposure to noxious stimuli such as hyperoxia, volutrauma, and infection in infancy can have long-reaching impacts on lung health and predispose towards the development of conditions such as chronic obstructive pulmonary disease (COPD) in adulthood. BPD and COPD are both marked by lung tissue degradation, neutrophil influx, and decreased lung function. Both diseases also express a change in microbial signature characterized by firmicute depletion. However, the relationship between pulmonary bacteria and the mechanisms of downstream disease development has yet to be elucidated. We hypothesized that murine models of BPD would show heightened acetylated proline-glycine-proline (Ac-PGP) pathway and neutrophil activity, and through gain- and loss-of-function studies we show that Ac-PGP plays a critical role in driving BPD development. We further test a inhaled live biotherapeutic (LBP) using active Lactobacillus strains in in vitro and in vivo models of BPD and COPD. The Lactobacillus-based LBP is effective in improving lung structure and function, mitigating neutrophil influx, and reducing a broad swath of pro-inflammatory markers in these models of chronic pulmonary disease via the MMP-9/PGP (matrix metalloproteinase/proline-glycine-proline) pathway. Inhaled LBPs show promise in addressing common pathways of disease progression that in the future can be targeted in a variety of chronic lung diseases.

Indexed as

Bronchopulmonary DysplasiaDisease Models, AnimalLactobacillusLungNeutrophilsPulmonary Disease, Chronic ObstructiveAdministration, InhalationAnimalsFemaleHumansMaleMiceMice, Inbred C57BLPneumoniaProbioticsProlineProline

Identifiers

PMID39160214
PMCPMC11333600

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.