dc.contributor.author | Xie, Wei | |
dc.contributor.author | Mondragon, Laura | |
dc.contributor.author | Mauseth, Brynjar | |
dc.contributor.author | Wang, Yan | |
dc.contributor.author | Pol, Jonathan | |
dc.contributor.author | Levesque, Sarah | |
dc.contributor.author | Zhou, Heng | |
dc.contributor.author | Yamazaki, Takahiro | |
dc.contributor.author | Eksteen, Jacobus Johannes | |
dc.contributor.author | Zitvogel, Laurence | |
dc.contributor.author | Sveinbjørnsson, Baldur | |
dc.contributor.author | Rekdal, Øystein | |
dc.contributor.author | Kepp, Oliver | |
dc.contributor.author | Kroemer, Guido | |
dc.date.accessioned | 2020-04-01T11:13:39Z | |
dc.date.available | 2020-04-01T11:13:39Z | |
dc.date.issued | 2019-04-13 | |
dc.description.abstract | Local immunotherapies such as the intratumoral injection of oncolytic compounds aim at reinstating and enhancing systemic anticancer immune responses. LTX-315 is a first-in-class, clinically evaluated oncolytic peptide-based local immunotherapy that meets these criteria. Here, we show that LTX-401, yet another oncolytic compound designed for local immunotherapy, depicts a similar safety profile and that sequential local inoculation of LTX-401 was able to cure immunocompetent host from subcutaneous MCA205 and TC-1 cancers. Cured animals exhibited long-term immune memory effects that rendered them resistant to rechallenge with syngeneic tumors. Nevertheless, the local treatment with LTX-401 alone had only limited abscopal effects on secondary contralateral lesions. Anticancer effects resulting from single as well as sequential injections of LTX-401 were boosted in combination with PD-1 and CTLA-4 immune checkpoint blockade (ICB), and sequential LTX-401 treatment combined with double ICB exhibited strong abscopal antineoplastic effects on contralateral tumors underlining the potency of this combination therapy. | en_US |
dc.description | This is an Accepted Manuscript of an article published by Taylor & Francis in <i>Oncoimmunology</i> on 13 April 2019, available online: <a href=https://www.tandfonline.com/doi/full/10.1080/2162402X.2019.1594555>https://www.tandfonline.com/doi/full/10.1080/2162402X.2019.1594555</a>. | en_US |
dc.identifier.citation | Xie W, Mondragon L, Mauseth B, Wang Y, Pol, Levesque, Zhou H, Yamazaki T, Eksteen JJ, Zitvogel L, Sveinbjørnsson B, Rekdal Ø, Kepp O, Kroemer G. Tumor lysis with LTX-401 creates anticancer immunity. Oncoimmunology. 2019;8(7) | en_US |
dc.identifier.cristinID | FRIDAID 1706784 | |
dc.identifier.doi | 10.1080/2162402X.2019.1594555 | |
dc.identifier.issn | 2162-4011 | |
dc.identifier.issn | 2162-402X | |
dc.identifier.uri | https://hdl.handle.net/10037/17961 | |
dc.language.iso | eng | en_US |
dc.publisher | Taylor & Francis | en_US |
dc.relation.journal | Oncoimmunology | |
dc.relation.projectID | info:eu-repo/grantAgreement/RCN/BIOTEK2021/254800/Norway/Verifying a New Generation of Oncolytic Peptides as Cancer Immunotherapeutic Agents for Deep-Seated Tumors// | en_US |
dc.relation.projectID | info:eu-repo/grantAgreement/RCN/NAERINGSPH/ 257967/Norway/Investigating a New Generation of Oncolytic Peptides as Cancer Immunotherapeutic Agents for Deep-Seated Tumors// | en_US |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2019 Taylor & Francis Group, LLC | en_US |
dc.subject | VDP::Medical disciplines: 700::Clinical medical disciplines: 750::Oncology: 762 | en_US |
dc.subject | VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Onkologi: 762 | en_US |
dc.title | Tumor lysis with LTX-401 creates anticancer immunity | en_US |
dc.type.version | acceptedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |