Publication:
Perspectives for clinical use of engineered human host defense antimicrobial peptides.

dc.contributor.authorPachón-Ibáñez, María Eugenia
dc.contributor.authorSmani, Younes
dc.contributor.authorPachón, Jerónimo
dc.contributor.authorSánchez-Céspedes, Javier
dc.date.accessioned2023-01-25T09:46:17Z
dc.date.available2023-01-25T09:46:17Z
dc.date.issued2017
dc.description.abstractInfectious diseases caused by bacteria, viruses or fungi are among the leading causes of death worldwide. The emergence of drug-resistance mechanisms, especially among bacteria, threatens the efficacy of all current antimicrobial agents, some of them already ineffective. As a result, there is an urgent need for new antimicrobial drugs. Host defense antimicrobial peptides (HDPs) are natural occurring and well-conserved peptides of innate immunity, broadly active against Gram-negative and Gram-positive bacteria, viruses and fungi. They also are able to exert immunomodulatory and adjuvant functions by acting as chemotactic for immune cells, and inducing cytokines and chemokines secretion. Moreover, they show low propensity to elicit microbial adaptation, probably because of their non-specific mechanism of action, and are able to neutralize exotoxins and endotoxins. HDPs have the potential to be a great source of novel antimicrobial agents. The goal of this review is to provide an overview of the advances made in the development of human defensins as well as the cathelicidin LL-37 and their derivatives as antimicrobial agents against bacteria, viruses and fungi for clinical use.
dc.identifier.doi10.1093/femsre/fux012
dc.identifier.essn1574-6976
dc.identifier.pmcPMC5435762
dc.identifier.pmid28521337
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435762/pdf
dc.identifier.unpaywallURLhttps://academic.oup.com/femsre/article-pdf/41/3/323/23906146/fux012.pdf
dc.identifier.urihttp://hdl.handle.net/10668/11209
dc.issue.number3
dc.journal.titleFEMS microbiology reviews
dc.journal.titleabbreviationFEMS Microbiol Rev
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number323-342
dc.pubmedtypeJournal Article
dc.pubmedtypeReview
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectantibacterial
dc.subjectantifungal
dc.subjectantiviral
dc.subjectcathelicidin
dc.subjectdefensins
dc.subjectinfectious diseases
dc.subject.meshAnti-Infective Agents
dc.subject.meshAntimicrobial Cationic Peptides
dc.subject.meshBacteria
dc.subject.meshBacterial Infections
dc.subject.meshDefensins
dc.subject.meshEndotoxins
dc.subject.meshExotoxins
dc.subject.meshFungi
dc.subject.meshHumans
dc.subject.meshMicrobial Sensitivity Tests
dc.subject.meshMycoses
dc.subject.meshVirus Diseases
dc.subject.meshViruses
dc.subject.meshCathelicidins
dc.titlePerspectives for clinical use of engineered human host defense antimicrobial peptides.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number41
dspace.entity.typePublication

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