Please use this identifier to cite or link to this item: https://doi.org/10.1042/BSR20193220
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dc.titleEngineering anti-cancer nanovaccine based on antigen cross-presentation
dc.contributor.authorWarrier, V.U.
dc.contributor.authorMakandar, A.I.
dc.contributor.authorGarg, M.
dc.contributor.authorSethi, G.
dc.contributor.authorKant, R.
dc.contributor.authorPal, J.K.
dc.contributor.authorYuba, E.
dc.contributor.authorGupta, R.K.
dc.date.accessioned2021-12-09T03:01:02Z
dc.date.available2021-12-09T03:01:02Z
dc.date.issued2019
dc.identifier.citationWarrier, V.U., Makandar, A.I., Garg, M., Sethi, G., Kant, R., Pal, J.K., Yuba, E., Gupta, R.K. (2019). Engineering anti-cancer nanovaccine based on antigen cross-presentation. Bioscience Reports 39 (10) : BSR20193220. ScholarBank@NUS Repository. https://doi.org/10.1042/BSR20193220
dc.identifier.issn0144-8463
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/209926
dc.description.abstractDendritic cells (DCs) present exogenous antigens on major histocompatibility complex (MHC) class I molecules, thereby activating CD8+ T cells, contributing to tumor elimination through a mechanism known as antigen cross-presentation. A variety of factors such as maturation state of DCs, co-stimulatory signals, T-cell microenvironment, antigen internalization routes and adjuvants regulate the process of DC-mediated antigen cross-presentation. Recently, the development of successful cancer immunotherapies may be attributed to the ability of DCs to cross-present tumor antigens. In this review article, we focus on the underlying mechanism of antigen cross-presentation and ways to improve antigen cross-presentation in different DC subsets. We have critically summarized the recent developments in the generation of novel nanovaccines for robust CD8+ T-cell response in cancer. In this context, we have reviewed nanocarriers that have been used for cancer immunotherapeutics based on antigen cross-presentation mechanism. Additionally, we have also expressed our views on the future applications of this mechanism in curing cancer. © 2019 The Author(s).
dc.publisherPortland Press Ltd
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2019
dc.typeReview
dc.contributor.departmentPHARMACOLOGY
dc.description.doi10.1042/BSR20193220
dc.description.sourcetitleBioscience Reports
dc.description.volume39
dc.description.issue10
dc.description.pageBSR20193220
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