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dc.contributor.authorBerkeley, RA
dc.contributor.authorSteele, LP
dc.contributor.authorMulder, AA
dc.contributor.authorvan den Wollenberg, DJM
dc.contributor.authorKottke, TJ
dc.contributor.authorThompson, J
dc.contributor.authorCoffey, M
dc.contributor.authorHoeben, RC
dc.contributor.authorVile, RG
dc.contributor.authorMelcher, A
dc.contributor.authorIlett, EJ
dc.date.accessioned2019-02-26T11:47:38Z
dc.date.issued2018-10-01
dc.identifier.citationCancer immunology research, 2018, 6 (10), pp. 1161 - 1173
dc.identifier.issn2326-6066
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3096
dc.identifier.eissn2326-6074
dc.identifier.doi10.1158/2326-6066.cir-18-0309
dc.description.abstractImmunotherapy is showing promise for otherwise incurable cancers. Oncolytic viruses (OVs), developed as direct cytotoxic agents, mediate their antitumor effects via activation of the immune system. However, OVs also stimulate antiviral immune responses, including the induction of OV-neutralizing antibodies. Current dogma suggests that the presence of preexisting antiviral neutralizing antibodies in patients, or their development during viral therapy, is a barrier to systemic OV delivery, rendering repeat systemic treatments ineffective. However, we have found that human monocytes loaded with preformed reovirus-antibody complexes, in which the reovirus is fully neutralized, deliver functional replicative reovirus to tumor cells, resulting in tumor cell infection and lysis. This delivery mechanism is mediated, at least in part, by antibody receptors (in particular FcγRIII) that mediate uptake and internalization of the reovirus/antibody complexes by the monocytes. This finding has implications for oncolytic virotherapy and for the design of clinical OV treatment strategies. Cancer Immunol Res; 6(10); 1161-73. ©2018 AACR.
dc.formatPrint-Electronic
dc.format.extent1161 - 1173
dc.languageeng
dc.language.isoeng
dc.publisherAMER ASSOC CANCER RESEARCH
dc.rights.urihttps://www.rioxx.net/licenses/under-embargo-all-rights-reserved
dc.subjectMonocytes
dc.subjectCell Line
dc.subjectAnimals
dc.subjectMice, Inbred C57BL
dc.subjectHumans
dc.subjectReoviridae
dc.subjectMelanoma, Experimental
dc.subjectImmunoglobulin A
dc.subjectImmunoglobulin G
dc.subjectReceptors, IgG
dc.subjectAntibodies, Viral
dc.subjectFemale
dc.subjectOncolytic Virotherapy
dc.subjectOncolytic Viruses
dc.subjectAntibodies, Neutralizing
dc.subjectChlorocebus aethiops
dc.titleAntibody-Neutralized Reovirus Is Effective in Oncolytic Virotherapy.
dc.typeJournal Article
dcterms.dateAccepted2018-08-16
rioxxterms.versionofrecord10.1158/2326-6066.cir-18-0309
rioxxterms.licenseref.urihttps://www.rioxx.net/licenses/under-embargo-all-rights-reserved
rioxxterms.licenseref.startdate2018-10
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfCancer immunology research
pubs.issue10
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Immunotherapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Immunotherapy/Translational Immunotherapy (TL)
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Immunotherapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Immunotherapy/Translational Immunotherapy (TL)
pubs.publication-statusPublished
pubs.volume6
pubs.embargo.termsNot known
icr.researchteamTranslational Immunotherapy
dc.contributor.icrauthorMelcher, Alan


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