Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/93040

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dc.contributor.authorTurner, Paul E.por
dc.contributor.authorAzeredo, Joanapor
dc.contributor.authorBuurman, Ed. T.por
dc.contributor.authorGreen, Sabrinapor
dc.contributor.authorHaaber, Jakob Krausepor
dc.contributor.authorHaggstrom, Douglaspor
dc.contributor.authorCarvalho, Koichi Kameda de Figueiredopor
dc.contributor.authorKirchhelle, Claaspor
dc.contributor.authorMoreno, Mercedes Gonzalezpor
dc.contributor.authorPirnay, Jean-Paulpor
dc.contributor.authorPortillo, Mirza Alaspor
dc.date.accessioned2024-09-12T15:56:27Z-
dc.date.available2024-09-12T15:56:27Z-
dc.date.issued2024-03-18-
dc.identifier.citationTurner, P. E., Azeredo, J., Buurman, E. T., Green, S., Haaber, J. K., Haggstrom, D., … Portillo, M. A. (2024, March 1). Addressing the Research and Development Gaps in Modern Phage Therapy. Phage. Mary Ann Liebert Inc. http://doi.org/10.1089/phage.2023.0045por
dc.identifier.issn2641-6530por
dc.identifier.urihttps://hdl.handle.net/1822/93040-
dc.description.abstractAntimicrobial resistance is on the rise globally, prompting increased research and development (R&D) of phage therapy as a strategy to address difficult-to-treat bacterial infections. We review the current state of phage therapy research, including major operational, epistemic, and biological challenges for phage R&D, and discuss some new approaches to developing the technology motivated by recent breakthroughs such as artificial intelligence and synthetic phage production. In addition, we contextualize these R&D challenges and opportunities in light of the ongoing predicament of commercial antimicrobial innovation and current publicprivate efforts to reinvigorate the pipeline of antimicrobial drug discovery. We conclude with reflections on the potential for new phage therapies to be readily accessible across all income contexts to better ensure broad patient access, and consider possible alternatives to current public and publicprivate solutions for phage therapy and production.por
dc.description.sponsorshipResearch reported in this publication is supported by CARB-X. CARB-X’s funding for this project is provided in part with federal funds from the U.S. Department of Health and Human Services, Administration for Strategic Preparedness and Response, BARDA, under agreement number: 75A50122C00028, and by an award from Wellcome (WT224842). K.K.F.C. was supported by PHAG-ONE (Agence Nationale de la Recherche). C.K. was supported by Wellcome Trust University Award (218118_Z_19_Z(2)). The contribution from M.G.M. to this project was made possible with funds from the Leibniz Competition, project T134/2022, of the Leibniz Association.por
dc.language.isoengpor
dc.publisherMary Ann Liebertpor
dc.rightsopenAccesspor
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/por
dc.subjectantimicrobial resistancepor
dc.subjectbiofilmpor
dc.subjectbiotechnologypor
dc.subjectpatient accesspor
dc.subjectpersonalized medicinepor
dc.titleAddressing the research and development gaps in modern phage therapypor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttps://www.liebertpub.com/doi/10.1089/phage.2023.0045por
dc.commentsCEB57656por
oaire.citationIssue1por
oaire.citationVolume5por
dc.date.updated2024-09-12T11:02:08Z-
dc.identifier.eissn2641-6549por
dc.identifier.doi10.1089/phage.2023.0045por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersion-
sdum.journalPHAGE: Therapy; Applications; and Researchpor
oaire.versionVoRpor
Aparece nas coleções:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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