Biohybrid Vaccines for Improved Treatment of Aggressive Melanoma with Checkpoint Inhibitor

dc.contributor.authorFontana F
dc.contributor.authorFusciello M
dc.contributor.authorGroeneveldt C
dc.contributor.authorCapasso C
dc.contributor.authorChiaro J
dc.contributor.authorFeola S
dc.contributor.authorLiu ZH
dc.contributor.authorMäkilä EM
dc.contributor.authorSalonen JJ
dc.contributor.authorHirvonen JT
dc.contributor.authorCerullo V
dc.contributor.authorSantos HA
dc.contributor.organizationfi=teollisuusfysiikan laboratorio|en=Laboratory of Industrial Physics|
dc.contributor.organization-code1.2.246.10.2458963.20.66904373678
dc.converis.publication-id41360158
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/41360158
dc.date.accessioned2022-10-27T12:27:20Z
dc.date.available2022-10-27T12:27:20Z
dc.description.abstractRecent approaches in the treatment of cancer focus on involving the immune system to control the tumor growth. The administration of immunotherapies, like checkpoint inhibitors, has shown impressive results in the long term survival of patients. Cancer vaccines are being investigated as further tools to prime tumor-specific immunity. Biomaterials show potential as adjuvants in the formulation of vaccines, and biomimetic elements derived from the membrane of tumor cells may widen the range of antigens contained in the vaccine. Here, we show how mice presenting an aggressive melanoma tumor model treated twice with the complete nanovaccine formulation showed control on the tumor progression, while in a less aggressive model, the animals showed remission and control on the tumor progression, with a modification in the immunological profile of the tumor microenvironment. We also prove that co-administration of the nanovaccine together with a checkpoint inhibitor increases the efficacy of the treatment (87.5% of the animals responding, with 2 remissions) compared to the checkpoint inhibitor alone in the B16.0VA model. Our platform thereby shows potential applications as a cancer nanovaccine in combination with the standard clinical care treatment for melanoma cancers.
dc.format.pagerange6477
dc.format.pagerange6490
dc.identifier.jour-issn1936-0851
dc.identifier.olddbid175620
dc.identifier.oldhandle10024/158714
dc.identifier.urihttps://www.utupub.fi/handle/11111/31045
dc.identifier.urnURN:NBN:fi-fe2021042823860
dc.language.isoen
dc.okm.affiliatedauthorMäkilä, Ermei
dc.okm.affiliatedauthorSalonen, Jarno
dc.okm.discipline114 Physical sciencesen_GB
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.discipline221 Nanotechnologyen_GB
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline114 Fysiikkafi_FI
dc.okm.discipline116 Kemiafi_FI
dc.okm.discipline221 Nanoteknologiafi_FI
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherAMER CHEMICAL SOC
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1021/acsnano.8b09613
dc.relation.ispartofjournalACS Nano
dc.relation.issue6
dc.relation.volume13
dc.source.identifierhttps://www.utupub.fi/handle/10024/158714
dc.titleBiohybrid Vaccines for Improved Treatment of Aggressive Melanoma with Checkpoint Inhibitor
dc.year.issued2019

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