Engineering synthetic breath biomarkers for respiratory disease

Human breath contains many volatile metabolites. However, few breath tests are currently used in the clinic to monitor disease due to bottlenecks in biomarker identification. Here we engineered breath biomarkers for respiratory disease by local delivery of protease-sensing nanoparticles to the lungs...

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Published inNature nanotechnology Vol. 15; no. 9; pp. 792 - 800
Main Authors Chan, Leslie W., Anahtar, Melodi N., Ong, Ta-Hsuan, Hern, Kelsey E., Kunz, Roderick R., Bhatia, Sangeeta N.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.09.2020
Nature Publishing Group
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Abstract Human breath contains many volatile metabolites. However, few breath tests are currently used in the clinic to monitor disease due to bottlenecks in biomarker identification. Here we engineered breath biomarkers for respiratory disease by local delivery of protease-sensing nanoparticles to the lungs. The nanosensors shed volatile reporters upon cleavage by neutrophil elastase, an inflammation-associated protease with elevated activity in lung diseases such as bacterial infection and alpha-1 antitrypsin deficiency. After intrapulmonary delivery into mouse models with acute lung inflammation, the volatile reporters are released and expelled in breath at levels detectable by mass spectrometry. These breath signals can identify diseased mice with high sensitivity as early as 10 min after nanosensor administration. Using these nanosensors, we performed serial breath tests to monitor dynamic changes in neutrophil elastase activity during lung infection and to assess the efficacy of a protease inhibitor therapy targeting neutrophil elastase for the treatment of alpha-1 antitrypsin deficiency. Volatile reporter molecules released by protease-sensing nanoparticles can serve as breath biomarkers for monitoring respiratory disease.
AbstractList Human breath contains many volatile metabolites. However, few breath tests are currently used in the clinic to monitor disease due to bottlenecks in biomarker identification. Here we engineered breath biomarkers for respiratory disease by local delivery of protease-sensing nanoparticles to the lungs. The nanosensors shed volatile reporters upon cleavage by neutrophil elastase, an inflammation-associated protease with elevated activity in lung diseases such as bacterial infection and alpha-1 antitrypsin deficiency. After intrapulmonary delivery into mouse models with acute lung inflammation, the volatile reporters are released and expelled in breath at levels detectable by mass spectrometry. These breath signals can identify diseased mice with high sensitivity as early as 10 min after nanosensor administration. Using these nanosensors, we performed serial breath tests to monitor dynamic changes in neutrophil elastase activity during lung infection and to assess the efficacy of a protease inhibitor therapy targeting neutrophil elastase for the treatment of alpha-1 antitrypsin deficiency. Volatile reporter molecules released by protease-sensing nanoparticles can serve as breath biomarkers for monitoring respiratory disease.
Human breath contains many volatile metabolites. However, few breath tests are currently used in the clinic to monitor disease due to bottlenecks in biomarker identification. Here we engineered breath biomarkers for respiratory disease by local delivery of protease-sensing nanoparticles to the lungs. The nanosensors shed volatile reporters upon cleavage by neutrophil elastase, an inflammation-associated protease with elevated activity in lung diseases such as bacterial infection and alpha-1 antitrypsin deficiency. After intrapulmonary delivery into mouse models with acute lung inflammation, the volatile reporters are released and expelled in breath at levels detectable by mass spectrometry. These breath signals can identify diseased mice with high sensitivity as early as 10 min after nanosensor administration. Using these nanosensors, we performed serial breath tests to monitor dynamic changes in neutrophil elastase activity during lung infection and to assess the efficacy of a protease inhibitor therapy targeting neutrophil elastase for the treatment of alpha-1 antitrypsin deficiency.Volatile reporter molecules released by protease-sensing nanoparticles can serve as breath biomarkers for monitoring respiratory disease.
Human breath contains many volatile metabolites. However, few breath tests are currently used in the clinic to monitor disease due to bottlenecks in biomarker identification. Here we engineered breath biomarkers for respiratory disease by local delivery of protease-sensing nanoparticles to the lungs. The nanosensors shed volatile reporters upon cleavage by neutrophil elastase, an inflammation-associated protease with elevated activity in lung diseases such as bacterial infection and alpha-1 antitrypsin deficiency. After intrapulmonary delivery into mouse models with acute lung inflammation, the volatile reporters are released and expelled in breath at levels detectable by mass spectrometry. These breath signals can identify diseased mice with high sensitivity as early as 10 min after nanosensor administration. Using these nanosensors, we performed serial breath tests to monitor dynamic changes in neutrophil elastase activity during lung infection and to assess the efficacy of a protease inhibitor therapy targeting neutrophil elastase for the treatment of alpha-1 antitrypsin deficiency.
Author Chan, Leslie W.
Ong, Ta-Hsuan
Kunz, Roderick R.
Bhatia, Sangeeta N.
Anahtar, Melodi N.
Hern, Kelsey E.
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  surname: Anahtar
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  surname: Hern
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  organization: Harvard–MIT Division of Health Sciences and Technology, Institute for Medical Engineering and Science, Massachusetts Institute of Technology
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  givenname: Roderick R.
  surname: Kunz
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  organization: Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Harvard–MIT Division of Health Sciences and Technology, Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Broad Institute, Massachusetts Institute of Technology and Harvard, Howard Hughes Medical Institute
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32690884$$D View this record in MEDLINE/PubMed
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Snippet Human breath contains many volatile metabolites. However, few breath tests are currently used in the clinic to monitor disease due to bottlenecks in biomarker...
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SubjectTerms 631/61/350
631/61/54
alpha 1-Antitrypsin Deficiency - drug therapy
alpha 1-Antitrypsin Deficiency - enzymology
alpha 1-Antitrypsin Deficiency - genetics
Animal models
Animals
Bacterial diseases
Biomarkers
Biomarkers - analysis
Breath tests
Breath Tests - instrumentation
Breath Tests - methods
Bronchopulmonary infection
Chemistry and Materials Science
Computer Simulation
Disease
Dose-Response Relationship, Drug
Drug Carriers - administration & dosage
Drug Carriers - chemistry
Elastase
Female
Glycine - analogs & derivatives
Glycine - pharmacology
Humans
Leukocyte Elastase - antagonists & inhibitors
Leukocyte Elastase - metabolism
Lung diseases
Lung Diseases - enzymology
Lung Diseases - microbiology
Mass Spectrometry
Mass spectroscopy
Materials Science
Metabolites
Mice, Inbred Strains
Mice, Knockout
Nanoparticles
Nanostructures - chemistry
Nanotechnology
Nanotechnology and Microengineering
Neutrophils
Polyethylene Glycols - chemistry
Protease
Protease inhibitors
Proteinase inhibitors
Pseudomonas Infections - enzymology
Respiratory diseases
Sulfonamides - pharmacology
Volatile Organic Compounds - analysis
Volatile Organic Compounds - chemistry
Volatile Organic Compounds - metabolism
Title Engineering synthetic breath biomarkers for respiratory disease
URI https://link.springer.com/article/10.1038/s41565-020-0723-4
https://www.ncbi.nlm.nih.gov/pubmed/32690884
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Volume 15
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