Interactions between microbiome and lungs: Paving new paths for microbiome based bio-engineered drug delivery systems in chronic respiratory diseases.

Drug delivery Engineered microbiome-derived therapeutics Gut-lung axis Microbiome Respiratory disease

Journal

Chemico-biological interactions
ISSN: 1872-7786
Titre abrégé: Chem Biol Interact
Pays: Ireland
ID NLM: 0227276

Informations de publication

Date de publication:
01 Sep 2019
Historique:
received: 25 04 2019
revised: 18 06 2019
accepted: 01 07 2019
pubmed: 6 7 2019
medline: 10 9 2019
entrez: 6 7 2019
Statut: ppublish

Résumé

The human body is a home to thousands of microbiotas. It is defined as a community of symbiotic, commensal and pathogenic microorganisms that have existed in all exposed sites of the body, which have co-evolved with diet, lifestyle, genetic factors and immune factors. Human microbiotas have been studied for years on their effects with relation to health and diseases. Relevant published studies, literature and reports were searched from accessible electronic databases and related institutional databases. We used keywords, viz; microbiome, microbiota, microbiome drug delivery and respiratory disease. Selected articles were carefully read through, clustered, segregated into subtopics and reviewed. The traditional belief of sterile lungs was challenged by the emergence of culture-independent molecular techniques and the recently introduced invasive broncho-alveolar lavage (BAL) sampling method. The constitution of a lung microbiome mainly depends on three main ecological factors, which include; firstly, the immigration of microbes into airways, secondly, the removal of microbes from airways and lastly, the regional growth conditions. In healthy conditions, the microbial communities that co-exist in our lungs can build significant pulmonary immunity and could act as a barrier against diseases, whereas, in an adverse way, microbiomes may interact with other pathogenic bacteriomes and viromes, acting as a cofactor in inflammation and host immune responses, which may lead to the progression of a disease. Thus, the use of microbiota as a target, and as a drug delivery system in the possible modification of a disease state, has started to gain massive attention in recent years. Microbiota, owing to its unique characteristics, could serve as a potential drug delivery system, that could be bioengineered to suit the interest. The engineered microbiome-derived therapeutics can be delivered through BC, bacteriophage, bacteria-derived lipid vesicles and microbe-derived extracellular vesicles. This review highlights the relationships between microbiota and different types of respiratory diseases, the importance of microbiota towards human health and diseases, including the role of novel microbiome drug delivery systems in targeting various respiratory diseases.

Sections du résumé

BACKGROUND BACKGROUND
The human body is a home to thousands of microbiotas. It is defined as a community of symbiotic, commensal and pathogenic microorganisms that have existed in all exposed sites of the body, which have co-evolved with diet, lifestyle, genetic factors and immune factors. Human microbiotas have been studied for years on their effects with relation to health and diseases.
METHODS METHODS
Relevant published studies, literature and reports were searched from accessible electronic databases and related institutional databases. We used keywords, viz; microbiome, microbiota, microbiome drug delivery and respiratory disease. Selected articles were carefully read through, clustered, segregated into subtopics and reviewed.
FINDINGS RESULTS
The traditional belief of sterile lungs was challenged by the emergence of culture-independent molecular techniques and the recently introduced invasive broncho-alveolar lavage (BAL) sampling method. The constitution of a lung microbiome mainly depends on three main ecological factors, which include; firstly, the immigration of microbes into airways, secondly, the removal of microbes from airways and lastly, the regional growth conditions. In healthy conditions, the microbial communities that co-exist in our lungs can build significant pulmonary immunity and could act as a barrier against diseases, whereas, in an adverse way, microbiomes may interact with other pathogenic bacteriomes and viromes, acting as a cofactor in inflammation and host immune responses, which may lead to the progression of a disease. Thus, the use of microbiota as a target, and as a drug delivery system in the possible modification of a disease state, has started to gain massive attention in recent years. Microbiota, owing to its unique characteristics, could serve as a potential drug delivery system, that could be bioengineered to suit the interest. The engineered microbiome-derived therapeutics can be delivered through BC, bacteriophage, bacteria-derived lipid vesicles and microbe-derived extracellular vesicles. This review highlights the relationships between microbiota and different types of respiratory diseases, the importance of microbiota towards human health and diseases, including the role of novel microbiome drug delivery systems in targeting various respiratory diseases.

Identifiants

pubmed: 31276660
pii: S0009-2797(19)30699-4
doi: 10.1016/j.cbi.2019.108732
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

108732

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Dinesh Kumar Chellappan (DK)

Department of Life Sciences, School of Pharmacy, International Medical University, Kuala Lumpur, 57000, Malaysia. Electronic address: Dinesh_Kumar@imu.edu.my.

Quinnie Ling Sze Ning (QL)

School of Pharmacy, International Medical University, Kuala Lumpur, 57000, Malaysia.

Sandra Khoo Su Min (SK)

School of Pharmacy, International Medical University, Kuala Lumpur, 57000, Malaysia.

Saw Yan Bin (SY)

School of Pharmacy, International Medical University, Kuala Lumpur, 57000, Malaysia.

Pang Jia Chern (PJ)

School of Pharmacy, International Medical University, Kuala Lumpur, 57000, Malaysia.

Tan Pei Shi (TP)

School of Pharmacy, International Medical University, Kuala Lumpur, 57000, Malaysia.

Sylvia Wong Ee Mei (SW)

School of Pharmacy, International Medical University, Kuala Lumpur, 57000, Malaysia.

Tan Hui Yee (TH)

School of Pharmacy, International Medical University, Kuala Lumpur, 57000, Malaysia.

Ong Jing Qi (OJ)

School of Pharmacy, International Medical University, Kuala Lumpur, 57000, Malaysia.

Lakshmi Thangavelu (L)

Saveetha Dental College and Hospitals, Saveetha University, SIMATS, Chennai, Tamil Nadu, India.

S Rajeshkumar (S)

Saveetha Dental College and Hospitals, Saveetha University, SIMATS, Chennai, Tamil Nadu, India.

Poonam Negi (P)

School of Pharmaceutical Sciences, Shoolini University of Biotechnology and Management Sciences, Solan, India, 173229, India.

Jestin Chellian (J)

Department of Life Sciences, School of Pharmacy, International Medical University, Kuala Lumpur, 57000, Malaysia.

Ridhima Wadhwa (R)

Faculty of Life Sciences and Biotechnology, South Asian University, New Delhi, India.

Gaurav Gupta (G)

School of Pharmacy, Suresh Gyan Vihar University, Jagatpura, Mahal Road, Jaipur, India.

Trudi Collet (T)

Innovative Medicines Group, School of Clinical Sciences, Institute of Health and Biomedical Innovation, Faculty of Health, Queensland University of Technology, Brisbane, 4059, Australia.

Philip M Hansbro (PM)

Centre for Inflammation, Centenary Institute, Royal Prince Alfred Hospital, Missenden Rd, Sydney, NSW, 2050, Australia; School of Life Sciences, University of Technology Sydney, Sydney, NSW, Australia; Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute (HMRI) & School of Biomedical Sciences and Pharmacy, University of Newcastle, Callaghan, NSW, 2308, Australia.

Kamal Dua (K)

Centre for Inflammation, Centenary Institute, Royal Prince Alfred Hospital, Missenden Rd, Sydney, NSW, 2050, Australia; Discipline of Pharmacy, Graduate School of Health, University of Technology Sydney, Ultimo, NSW, 2007, Australia; Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute (HMRI) & School of Biomedical Sciences and Pharmacy, University of Newcastle, Callaghan, NSW, 2308, Australia. Electronic address: Kamal.Dua@uts.edu.au.

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Classifications MeSH