Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Nov 6;4(6):e00747-19.
doi: 10.1128/mSphere.00747-19.

Fungal Extracellular Vesicles as Potential Targets for Immune Interventions

Affiliations
Review

Fungal Extracellular Vesicles as Potential Targets for Immune Interventions

Mateus Silveira Freitas et al. mSphere. .

Abstract

The release of extracellular vesicles (EVs) by fungi is a fundamental cellular process. EVs carry several biomolecules, including pigments, proteins, enzymes, lipids, nucleic acids, and carbohydrates, and are involved in physiological and pathological processes. EVs may play a pivotal role in the establishment of fungal infections, as they can interact with the host immune system to elicit multiple outcomes. It has been observed that, depending on the fungal pathogen, EVs can exacerbate or attenuate fungal infections. The study of the interaction between fungal EVs and the host immune system and understanding of the mechanisms that regulate those interactions might be useful for the development of new adjuvants as well as the improvement of protective immune responses against infectious or noninfectious diseases. In this review, we describe the immunomodulatory properties of EVs produced by pathogenic fungi and discuss their potential as adjuvants for prophylactic or therapeutic strategies.

Keywords: drug targets; extracellular vesicles; fungal infections; immune response.

PubMed Disclaimer

Figures

FIG 1
FIG 1
Fungal EVs may play a pivotal role in the establishment of fungal infections and can alter the infection process. These EVs are potential targets for new antifungal agents, as well as potential candidates for chemotherapy and vaccine development.

References

    1. Deatherage BL, Cookson BT. 2012. Membrane vesicle release in bacteria, eukaryotes, and archaea: a conserved yet underappreciated aspect of microbial life. Infect Immun 80:1948–1957. doi:10.1128/IAI.06014-11. - DOI - PMC - PubMed
    1. Yáñez-Mó M, Siljander PR-M, Andreu Z, Zavec AB, Borràs FE, Buzas EI, Buzas K, Casal E, Cappello F, Carvalho J, Colás E, Cordeiro-da Silva A, Fais S, Falcon-Perez JM, Ghobrial IM, Giebel B, Gimona M, Graner M, Gursel I, Gursel M, Heegaard NHH, Hendrix A, Kierulf P, Kokubun K, Kosanovic M, Kralj-Iglic V, Krämer-Albers E-M, Laitinen S, Lässer C, Lener T, Ligeti E, Linē A, Lipps G, Llorente A, Lötvall J, Manček-Keber M, Marcilla A, Mittelbrunn M, Nazarenko I, Nolte-'t Hoen ENM, Nyman TA, O'Driscoll L, Olivan M, Oliveira C, Pállinger É, Del Portillo HA, Reventós J, Rigau M, Rohde E, Sammar M, et al. . 2015. Biological properties of extracellular vesicles and their physiological functions. J Extracell Vesicles 4:27066. doi:10.3402/jev.v4.27066. - DOI - PMC - PubMed
    1. van Niel G, D'Angelo G, Raposo G. 2018. Shedding light on the cell biology of extracellular vesicles. Nat Rev Mol Cell Biol 19:213–228. doi:10.1038/nrm.2017.125. - DOI - PubMed
    1. Brock CK, Wallin ST, Ruiz OE, Samms KM, Mandal A, Sumner EA, Eisenhoffer GT. 2019. Stem cell proliferation is induced by apoptotic bodies from dying cells during epithelial tissue maintenance. Nat Commun 10:1044. doi:10.1038/s41467-019-09010-6. - DOI - PMC - PubMed
    1. Malloci M, Perdomo L, Veerasamy M, Andriantsitohaina R, Simard G, Martinez MC. 2019. Extracellular vesicles: mechanisms in human health and disease. Antioxid Redox Signal 30:813–856. doi:10.1089/ars.2017.7265. - DOI - PubMed

Publication types

MeSH terms

Substances