Back to Search Start Over

Host and Pathogen-Directed Therapies against Microbial Infections Using Exosome- and Antimicrobial Peptide-derived Stem Cells with a Special look at Pulmonary Infections and Sepsis.

Authors :
Moosazadeh Moghaddam, Mehrdad
Fazel, Parvindokht
Fallah, Arezoo
Sedighian, Hamid
Kachuei, Reza
Behzadi, Elham
Imani Fooladi, Abbas Ali
Source :
Stem Cell Reviews & Reports. Oct2023, Vol. 19 Issue 7, p2166-2191. 26p.
Publication Year :
2023

Abstract

Microbial diseases are a great threat to global health and cause considerable mortality and extensive economic losses each year. The medications for treating this group of diseases (antibiotics, antiviral, antifungal drugs, etc.) directly attack the pathogenic agents by recognizing the target molecules. However, it is necessary to note that excessive use of any of these drugs can lead to an increase in microbial resistance and infectious diseases. New therapeutic methods have been studied recently using emerging drugs such as mesenchymal stem cell-derived exosomes (MSC-Exos) and antimicrobial peptides (AMPs), which act based on two completely different strategies against pathogens including Host-Directed Therapy (HDT) and Pathogen-Directed Therapy (PDT), respectively. In the PDT approach, AMPs interact directly with pathogens to interrupt their intrusion, survival, and proliferation. These drugs interact directly with the cell membrane or intracellular components of pathogens and cause the death of pathogens or inhibit their replication. The mechanism of action of MSC-Exos in HDT is based on immunomodulation and regulation, promotion of tissue regeneration, and reduced host toxicity. This review studies the potential of mesenchymal stem cell-derived exosomes/ATPs therapeutic properties against microbial infectious diseases especially pulmonary infections and sepsis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15508943
Volume :
19
Issue :
7
Database :
Academic Search Index
Journal :
Stem Cell Reviews & Reports
Publication Type :
Academic Journal
Accession number :
173016949
Full Text :
https://doi.org/10.1007/s12015-023-10594-2