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 in | Nature nanotechnology Vol. 15; no. 9; pp. 792 - 800 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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. |
Author_xml | – sequence: 1 givenname: Leslie W. surname: Chan fullname: Chan, Leslie W. organization: Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology – sequence: 2 givenname: Melodi N. surname: Anahtar fullname: Anahtar, Melodi N. 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 – sequence: 3 givenname: Ta-Hsuan surname: Ong fullname: Ong, Ta-Hsuan organization: Biological and Chemical Technologies Group, Massachusetts Institute of Technology Lincoln Laboratory – sequence: 4 givenname: Kelsey E. surname: Hern fullname: Hern, Kelsey E. organization: Harvard–MIT Division of Health Sciences and Technology, Institute for Medical Engineering and Science, Massachusetts Institute of Technology – sequence: 5 givenname: Roderick R. surname: Kunz fullname: Kunz, Roderick R. organization: Biological and Chemical Technologies Group, Massachusetts Institute of Technology Lincoln Laboratory – sequence: 6 givenname: Sangeeta N. orcidid: 0000-0002-1293-2097 surname: Bhatia fullname: Bhatia, Sangeeta N. email: sbhatia@mit.edu 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 |
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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 |
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