Rodyti trumpą aprašą

dc.contributor.authorBalevičiūtė, Austėja
dc.contributor.authorRadzevičiūtė, Eivina
dc.contributor.authorŽelvys, Augustinas
dc.contributor.authorMalyško-Ptašinskė, Veronika
dc.contributor.authorNovickij, Jurij
dc.contributor.authorZinkevičienė, Auksė
dc.contributor.authorKašėta, Vytautas
dc.contributor.authorNovickij, Vitalij
dc.contributor.authorGirkontaitė, Irutė
dc.date.accessioned2023-09-18T16:26:39Z
dc.date.available2023-09-18T16:26:39Z
dc.date.issued2022
dc.identifier.other(WOS_ID)000900598100001
dc.identifier.urihttps://etalpykla.vilniustech.lt/handle/123456789/114019
dc.description.abstractIn this work, a time-dependent and time-independent study on bleomycin-based high-frequency nsECT (3.5 kV/cm × 200 pulses) for the elimination of LLC1 tumours in C57BL/6J mice is performed. We show the efficiency of nsECT (200 ns and 700 ns delivered at 1 kHz and 1 MHz) for the elimination of tumours in mice and increase of their survival. The dynamics of the immunomodulatory effects were observed after electrochemotherapy by investigating immune cell populations and antitumour antibodies at different timepoints after the treatment. ECT treatment resulted in an increased percentage of CD4+ T, splenic memory B and tumour-associated dendritic cell subsets. Moreover, increased levels of antitumour IgG antibodies after ECT treatment were detected. Based on the time-dependent study results, nsECT treatment upregulated PD 1 expression on splenic CD4+ Tr1 cells, increased the expansion of splenic CD8+ T, CD4+CD8+ T, plasma cells and the proportion of tumour-associated pro inflammatory macrophages. The Lin− population of immune cells that was increased in the spleens and tumour after nsECT was identified. It was shown that nsECT prolonged survival of the treated mice and induced significant changes in the immune system, which shows a promising alliance of nanosecond electrochemotherapy and immunotherapy.eng
dc.formatPDF
dc.format.extentp. 1-26
dc.format.mediumtekstas / txt
dc.language.isoeng
dc.relation.isreferencedbyScience Citation Index Expanded (Web of Science)
dc.relation.isreferencedbyScopus
dc.relation.isreferencedbyPubMed
dc.titleHigh-frequency nanosecond bleomycin electrochemotherapy and its effects on changes in the immune system and survival
dc.typeStraipsnis Web of Science DB / Article in Web of Science DB
dcterms.accessRightsThis article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).
dcterms.licenseCreative Commons – Attribution – 4.0 International
dcterms.references113
dc.type.pubtypeS1 - Straipsnis Web of Science DB / Web of Science DB article
dc.contributor.institutionKarolinska Institutet Valstybinis mokslinių tyrimų institutas Inovatyvios medicinos centras
dc.contributor.institutionValstybinis mokslinių tyrimų institutas Inovatyvios medicinos centras
dc.contributor.institutionVilniaus Gedimino technikos universitetas
dc.contributor.institutionValstybinis mokslinių tyrimų institutas Inovatyvios medicinos centras Vilniaus Gedimino technikos universitetas
dc.contributor.facultyElektronikos fakultetas / Faculty of Electronics
dc.subject.researchfieldT 001 - Elektros ir elektronikos inžinerija / Electrical and electronic engineering
dc.subject.researchfieldN 010 - Biologija / Biology
dc.subject.vgtuprioritizedfieldsFM0202 - Ląstelių ir jų biologiškai aktyvių komponentų tyrimai / Investigations on cells and their biologically active components
dc.subject.ltspecializationsL105 - Sveikatos technologijos ir biotechnologijos / Health technologies and biotechnologies
dc.subject.ennanosecond
dc.subject.enelectroporation
dc.subject.enelectrochemotherapy
dc.subject.enin vivo
dc.subject.enbleomycin
dc.subject.enpulsed electric fields
dc.subject.enimmunology
dc.subject.enimmunomodulation
dc.subject.enanticancer
dc.subject.enhumoral and cellular immunity
dcterms.sourcetitleCancers
dc.description.issueiss. 24
dc.description.volumevol. 14
dc.publisher.nameMDPI
dc.publisher.cityBasel
dc.identifier.doi000900598100001
dc.identifier.doi143423735
dc.identifier.doi10.3390/cancers14246254
dc.identifier.elaba150926536


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