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Adjuvant ArtinM favored the host immunity against Cryptococcus gattii infection in C57BL/6 mice

dc.contributor.authorMartins Oliveira-Brito, Patrícia Kellen
dc.contributor.authorde Campos, Gabriela Yamazaki
dc.contributor.authorGuimarães, Júlia Garcia
dc.contributor.authorMachado, Michele Procópio
dc.contributor.authorSerafim, Letícia Costa
dc.contributor.authorLazo Chica, Javier Emílio
dc.contributor.authorRoque-Barreira, Maria Cristina
dc.contributor.authorda Silva, Thiago Aparecido [UNESP]
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionFederal University of Triângulo Mineiro
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T19:13:53Z
dc.date.issued2024-01-01
dc.description.abstractAim:Cryptococcus gattii causes a severe fungal infection with high mortality rate among immunosuppressed and immunocompetent individuals. Due to limitation of current antifungal treatment, new immunotherapeutic approaches are explored. Methods: This study investigated an immunization strategy utilizing heat-inactivated C. gattii with ArtinM as an adjuvant. C57BL/6 mice were intranasally immunized with heat-killed C. gattii and ArtinM was administrated either before immunization or along with HK-C. gattii. Mice were infected with C. gattii and the efficacy of the immunization protocol was evaluated. Results: Mice that received ArtinM exhibited increased levels of IL-10 and relative expression of IL-23 in the lungs, reduced fungal burden and preserved tissue integrity post-infection. Conclusion: Adjuvant ArtinM improved immunization against C. gattii infection in C57BL/6 mice.en
dc.description.affiliationDepartment of Cell & Molecular Biology & Pathogenic Bioagents Ribeirão Preto Medical School University of São Paulo, São Paulo
dc.description.affiliationMicrobiology Postgraduate Program of the Microbiology Department of the Biomedical Sciences Institute (ICB) of University of São Paulo, São Paulo
dc.description.affiliationInstitute of Natural & Biological Sciences Federal University of Triângulo Mineiro
dc.description.affiliationClinical Hematology Lab Department of Clinical Analysis School of Pharmaceutical Sciences in Araraquara (FCFAR) Sao Paulo State University (UNESP), São Paulo
dc.description.affiliationNational Institute of Science & Technology in Human Pathogenic Fungi School of Pharmaceutical Sciences of Ribeirao Preto University of São Paulo
dc.description.affiliationUnespClinical Hematology Lab Department of Clinical Analysis School of Pharmaceutical Sciences in Araraquara (FCFAR) Sao Paulo State University (UNESP), São Paulo
dc.format.extent733-748
dc.identifierhttp://dx.doi.org/10.1080/1750743X.2024.2360384
dc.identifier.citationImmunotherapy, v. 16, n. 11, p. 733-748, 2024.
dc.identifier.doi10.1080/1750743X.2024.2360384
dc.identifier.issn1750-7448
dc.identifier.issn1750-743X
dc.identifier.scopus2-s2.0-85197390748
dc.identifier.urihttps://hdl.handle.net/11449/302205
dc.language.isoeng
dc.relation.ispartofImmunotherapy
dc.sourceScopus
dc.subjectArtinM
dc.subjectCD14
dc.subjectCryptococcus gattii
dc.subjectimmunomodulation
dc.subjectlectin
dc.subjectTLR2
dc.subjectvaccine
dc.titleAdjuvant ArtinM favored the host immunity against Cryptococcus gattii infection in C57BL/6 miceen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0002-1406-4385[1]
unesp.author.orcid0000-0001-7143-0014[2]
unesp.author.orcid0000-0002-3928-0703[3]
unesp.author.orcid0000-0002-5751-2176[4]
unesp.author.orcid0000-0002-3973-7953[5]
unesp.author.orcid0000-0003-1950-1895[6]
unesp.author.orcid0000-0001-7425-0908[7]
unesp.author.orcid0000-0001-5017-6539[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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