Engineering anti-cancer nanovaccine based on antigen cross-presentation
Identifieur interne : 000B39 ( Ncbi/Merge ); précédent : 000B38; suivant : 000B40Engineering anti-cancer nanovaccine based on antigen cross-presentation
Auteurs : Vaishnavi U. Warrier ; Amina I. Makandar ; Manoj Garg ; Gautam Sethi ; Ravi Kant ; Jayanta K. Pal ; Eiji Yuba ; Rajesh Kumar GuptaSource :
- Bioscience Reports [ 0144-8463 ] ; 2019.
Abstract
Dendritic 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.
Url:
DOI: 10.1042/BSR20193220
PubMed: 31652460
PubMed Central: 6822533
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PMC:6822533Le document en format XML
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<series><title level="j">Bioscience Reports</title>
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<front><div type="abstract" xml:lang="en"><title>Abstract</title>
<p>Dendritic cells (DCs) present exogenous antigens on major histocompatibility complex (MHC) class I molecules, thereby activating CD8<sup>+</sup>
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<sup>+</sup>
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.</p>
</div>
</front>
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<pmc article-type="review-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Biosci Rep</journal-id>
<journal-id journal-id-type="iso-abbrev">Biosci. Rep</journal-id>
<journal-id journal-id-type="publisher-id">bsr</journal-id>
<journal-title-group><journal-title>Bioscience Reports</journal-title>
</journal-title-group>
<issn pub-type="ppub">0144-8463</issn>
<issn pub-type="epub">1573-4935</issn>
<publisher><publisher-name>Portland Press Ltd.</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">31652460</article-id>
<article-id pub-id-type="pmc">6822533</article-id>
<article-id pub-id-type="doi">10.1042/BSR20193220</article-id>
<article-id pub-id-type="publisher-id">BSR20193220</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Cancer</subject>
</subj-group>
<subj-group subj-group-type="heading"><subject>Therapeutics & Molecular Medicine</subject>
</subj-group>
<subj-group subj-group-type="heading"><subject>Immunology & Inflammation</subject>
</subj-group>
<subj-group subj-group-type="toc-heading"><subject>Review Articles</subject>
</subj-group>
</article-categories>
<title-group><article-title>Engineering anti-cancer nanovaccine based on antigen cross-presentation</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Warrier</surname>
<given-names>Vaishnavi U.</given-names>
</name>
<xref ref-type="aff" rid="AFF1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Makandar</surname>
<given-names>Amina I.</given-names>
</name>
<xref ref-type="aff" rid="AFF1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Garg</surname>
<given-names>Manoj</given-names>
</name>
<email>mgarg@amity.edu</email>
<xref ref-type="aff" rid="AFF2"></xref>
<xref ref-type="corresp" rid="COR1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Sethi</surname>
<given-names>Gautam</given-names>
</name>
<email>phcgs@nus.edu.sg</email>
<xref ref-type="aff" rid="AFF3"></xref>
<xref ref-type="corresp" rid="COR1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Kant</surname>
<given-names>Ravi</given-names>
</name>
<xref ref-type="aff" rid="AFF4"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Pal</surname>
<given-names>Jayanta K.</given-names>
</name>
<xref ref-type="aff" rid="AFF1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Yuba</surname>
<given-names>Eiji</given-names>
</name>
<xref ref-type="aff" rid="AFF5"></xref>
</contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid" authenticated="false">http://orcid.org/0000-0001-8820-0661</contrib-id>
<name><surname>Gupta</surname>
<given-names>Rajesh Kumar</given-names>
</name>
<email>guptarajesh76@gmail.com</email>
<xref ref-type="aff" rid="AFF1"></xref>
<xref ref-type="corresp" rid="COR1"></xref>
</contrib>
</contrib-group>
<aff id="AFF1"><label>1</label>
Protein Biochemistry Research Laboratory, Dr. D.Y. Patil Biotechnology and Bioinformatics Institute, Dr. D.Y. Patil Vidyapeeth (Deemed to be University), Tathawade, Pune 411033, Maharashtra, India</aff>
<aff id="AFF2"><label>2</label>
Amity Institute of Molecular Medicine and Stem Cell Research (AIMMSCR), Amity University, Noida 201313, Uttar Pradesh, India</aff>
<aff id="AFF3"><label>3</label>
Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600, Singapore</aff>
<aff id="AFF4"><label>4</label>
Experimental Neuroimmunology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany</aff>
<aff id="AFF5"><label>5</label>
Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Naka-ku, Sakai 599-8531, Osaka, Japan</aff>
<author-notes><corresp id="COR1"><bold>Correspondence:</bold>
Rajesh Kumar Gupta (<email>guptarajesh76@gmail.com</email>
) or Gautam Sethi (<email>phcgs@nus.edu.sg</email>
) or Manoj Garg (<email>mgarg@amity.edu</email>
)</corresp>
</author-notes>
<pub-date pub-type="collection"><day>30</day>
<month>10</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub" iso-8601-date="2019-10-18"><day>18</day>
<month>10</month>
<year>2019</year>
</pub-date>
<volume>39</volume>
<issue>10</issue>
<elocation-id>BSR20193220</elocation-id>
<history><date date-type="received"><day>10</day>
<month>9</month>
<year>2019</year>
</date>
<date date-type="rev-recd"><day>27</day>
<month>9</month>
<year>2019</year>
</date>
<date date-type="accepted"><day>01</day>
<month>10</month>
<year>2019</year>
</date>
</history>
<permissions><copyright-statement>© 2019 The Author(s).</copyright-statement>
<copyright-year>2019</copyright-year>
<license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/"><license-p>This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY).</license-p>
</license>
</permissions>
<self-uri xlink:href="bsr-39-bsr20193220.pdf"></self-uri>
<abstract><title>Abstract</title>
<p>Dendritic cells (DCs) present exogenous antigens on major histocompatibility complex (MHC) class I molecules, thereby activating CD8<sup>+</sup>
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<sup>+</sup>
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.</p>
</abstract>
<kwd-group><kwd>Antigen Cross-presentation</kwd>
<kwd>Cancer immunotherapy</kwd>
<kwd>DC-SIGN</kwd>
<kwd>Dendritic cell (DC)</kwd>
<kwd>Glycan</kwd>
<kwd>Nanocarriers</kwd>
</kwd-group>
<counts><page-count count="19"></page-count>
</counts>
</article-meta>
</front>
</pmc>
<affiliations><list></list>
<tree><noCountry><name sortKey="Garg, Manoj" sort="Garg, Manoj" uniqKey="Garg M" first="Manoj" last="Garg">Manoj Garg</name>
<name sortKey="Gupta, Rajesh Kumar" sort="Gupta, Rajesh Kumar" uniqKey="Gupta R" first="Rajesh Kumar" last="Gupta">Rajesh Kumar Gupta</name>
<name sortKey="Kant, Ravi" sort="Kant, Ravi" uniqKey="Kant R" first="Ravi" last="Kant">Ravi Kant</name>
<name sortKey="Makandar, Amina I" sort="Makandar, Amina I" uniqKey="Makandar A" first="Amina I." last="Makandar">Amina I. Makandar</name>
<name sortKey="Pal, Jayanta K" sort="Pal, Jayanta K" uniqKey="Pal J" first="Jayanta K." last="Pal">Jayanta K. Pal</name>
<name sortKey="Sethi, Gautam" sort="Sethi, Gautam" uniqKey="Sethi G" first="Gautam" last="Sethi">Gautam Sethi</name>
<name sortKey="Warrier, Vaishnavi U" sort="Warrier, Vaishnavi U" uniqKey="Warrier V" first="Vaishnavi U." last="Warrier">Vaishnavi U. Warrier</name>
<name sortKey="Yuba, Eiji" sort="Yuba, Eiji" uniqKey="Yuba E" first="Eiji" last="Yuba">Eiji Yuba</name>
</noCountry>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Ncbi/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000B39 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd -nk 000B39 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Sante |area= ChloroquineV1 |flux= Ncbi |étape= Merge |type= RBID |clé= PMC:6822533 |texte= Engineering anti-cancer nanovaccine based on antigen cross-presentation }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/RBID.i -Sk "pubmed:31652460" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd \ | NlmPubMed2Wicri -a ChloroquineV1
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