A simple self-adjuvanting biomimetic nanovaccine self-assembled with the conjugate of phospholipids and nucleotides can induce a strong cancer immunotherapeutic effect
Biomimetic nanoparticles have potential applications in many fields due to their favorable properties. Here, we developed a self-adjuvanting biomimetic anti-tumor nanovaccine, which was self-assembled with an amphiphilic conjugate synthesized with the phospholipids of 1,2-dioleoyl- sn-glycero -3-pho...
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Veröffentlicht in: | Biomaterials science 2021-01, Vol.9 (1), p.84-92 |
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creator | Liu, Dan Liu, Jiale Ma, Bing Deng, Bo Leng, Xigang Kong, Deling Liu, Lanxia |
description | Biomimetic nanoparticles have potential applications in many fields due to their favorable properties. Here, we developed a self-adjuvanting biomimetic anti-tumor nanovaccine, which was self-assembled with an amphiphilic conjugate synthesized with the phospholipids of 1,2-dioleoyl-
sn-glycero
-3-phosphoethanolamine (DOPE) and hydrophilic Toll-like receptor (TLR9) agonist CpG ODN. The nanovaccine could not only provide effective initial antigen stimulation and sustained long-term antigen supply with a controlled release, but also induce antigen cross-presentation
via
the MHC-I pathway initiating CD8
+
T-cell responses. Moreover, the dense nucleotide shell around the nanovaccine could promote antigen endocytosis
via
various receptor-mediated pathways into dendritic cells. CpG ODN interacted with TLR9 triggering the cytokine secretion of TNF-α and IL-10, which further boosted the anti-tumor humoral and cellular immune responses, which led to a significant tumor suppressive effect and remarkable survival prolongation. So, this nanovaccine self-assembled with phospholipid-nucleotide amphiphiles can serve as a safe, simple and efficient approach for anti-tumor immunotherapy.
The biomimetic nanovaccines not only promoted antigens endocytosis into dendritic cells
via
receptor-mediated pathways but also induced antigens cross-presentation eliciting CD8
+
T-cell responses. CPG-ODN as an adjuvant further enhanced the anti-tumor immune responses. |
doi_str_mv | 10.1039/d0bm01333a |
format | Article |
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sn-glycero
-3-phosphoethanolamine (DOPE) and hydrophilic Toll-like receptor (TLR9) agonist CpG ODN. The nanovaccine could not only provide effective initial antigen stimulation and sustained long-term antigen supply with a controlled release, but also induce antigen cross-presentation
via
the MHC-I pathway initiating CD8
+
T-cell responses. Moreover, the dense nucleotide shell around the nanovaccine could promote antigen endocytosis
via
various receptor-mediated pathways into dendritic cells. CpG ODN interacted with TLR9 triggering the cytokine secretion of TNF-α and IL-10, which further boosted the anti-tumor humoral and cellular immune responses, which led to a significant tumor suppressive effect and remarkable survival prolongation. So, this nanovaccine self-assembled with phospholipid-nucleotide amphiphiles can serve as a safe, simple and efficient approach for anti-tumor immunotherapy.
The biomimetic nanovaccines not only promoted antigens endocytosis into dendritic cells
via
receptor-mediated pathways but also induced antigens cross-presentation eliciting CD8
+
T-cell responses. CPG-ODN as an adjuvant further enhanced the anti-tumor immune responses.</description><identifier>ISSN: 2047-4830</identifier><identifier>EISSN: 2047-4849</identifier><identifier>DOI: 10.1039/d0bm01333a</identifier><identifier>PMID: 33016303</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Animals ; Antigens ; Biomimetics ; Conjugates ; Controlled release ; Cytokines ; Humans ; Immunotherapy ; Mice ; Mice, Inbred C57BL ; Nanoparticles ; Neoplasms - drug therapy ; Nucleotides ; Oligodeoxyribonucleotides ; Phospholipids ; Prolongation ; Receptors ; Self-assembly</subject><ispartof>Biomaterials science, 2021-01, Vol.9 (1), p.84-92</ispartof><rights>Copyright Royal Society of Chemistry 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-9821cb0ccfec4cb3e279c4c3883d5aa6cc00ce3123937c49205f1b78956475583</citedby><cites>FETCH-LOGICAL-c373t-9821cb0ccfec4cb3e279c4c3883d5aa6cc00ce3123937c49205f1b78956475583</cites><orcidid>0000-0002-8153-9678 ; 0000-0002-2961-9267</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33016303$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Dan</creatorcontrib><creatorcontrib>Liu, Jiale</creatorcontrib><creatorcontrib>Ma, Bing</creatorcontrib><creatorcontrib>Deng, Bo</creatorcontrib><creatorcontrib>Leng, Xigang</creatorcontrib><creatorcontrib>Kong, Deling</creatorcontrib><creatorcontrib>Liu, Lanxia</creatorcontrib><title>A simple self-adjuvanting biomimetic nanovaccine self-assembled with the conjugate of phospholipids and nucleotides can induce a strong cancer immunotherapeutic effect</title><title>Biomaterials science</title><addtitle>Biomater Sci</addtitle><description>Biomimetic nanoparticles have potential applications in many fields due to their favorable properties. Here, we developed a self-adjuvanting biomimetic anti-tumor nanovaccine, which was self-assembled with an amphiphilic conjugate synthesized with the phospholipids of 1,2-dioleoyl-
sn-glycero
-3-phosphoethanolamine (DOPE) and hydrophilic Toll-like receptor (TLR9) agonist CpG ODN. The nanovaccine could not only provide effective initial antigen stimulation and sustained long-term antigen supply with a controlled release, but also induce antigen cross-presentation
via
the MHC-I pathway initiating CD8
+
T-cell responses. Moreover, the dense nucleotide shell around the nanovaccine could promote antigen endocytosis
via
various receptor-mediated pathways into dendritic cells. CpG ODN interacted with TLR9 triggering the cytokine secretion of TNF-α and IL-10, which further boosted the anti-tumor humoral and cellular immune responses, which led to a significant tumor suppressive effect and remarkable survival prolongation. So, this nanovaccine self-assembled with phospholipid-nucleotide amphiphiles can serve as a safe, simple and efficient approach for anti-tumor immunotherapy.
The biomimetic nanovaccines not only promoted antigens endocytosis into dendritic cells
via
receptor-mediated pathways but also induced antigens cross-presentation eliciting CD8
+
T-cell responses. CPG-ODN as an adjuvant further enhanced the anti-tumor immune responses.</description><subject>Animals</subject><subject>Antigens</subject><subject>Biomimetics</subject><subject>Conjugates</subject><subject>Controlled release</subject><subject>Cytokines</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Nanoparticles</subject><subject>Neoplasms - drug therapy</subject><subject>Nucleotides</subject><subject>Oligodeoxyribonucleotides</subject><subject>Phospholipids</subject><subject>Prolongation</subject><subject>Receptors</subject><subject>Self-assembly</subject><issn>2047-4830</issn><issn>2047-4849</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkl1rFTEQhoMottTeeK8EvCmFtdmd_crlsbUqtHij10t2drYnh02y5qPiL_JvmnraIzgwZJg8eSfwDmOvS_G-FCAvJjEaUQKAesaOK1F3Rd3X8vmhBnHETkPYiRxdJ0VbvmRHAKJsQcAx-73hQZt1IR5omQs17dK9slHbOz5qZ7ShqJFbZd29QtT2iQuBzLjQxH_quOVxSxyd3aU7FYm7ma9bF3IuetVT4MpO3CZcyEU9UeCoLNd2Skhc8RC9y9NyD8lzbUyyLut5tVJ6mE3zTBhfsRezWgKdPp4n7Pv1x2-Xn4ubr5--XG5uCoQOYiH7qsRRIOY3NY5AVSdzAX0PU6NUiygEEpQVSOiwlpVo5nLsetm0ddc0PZyws73u6t2PRCEORgekZVGWXApDVdd9C61o24y--w_dueRt_l2mukbWsocmU-d7Cr0LwdM8rF4b5X8NpRgeHByuxIfbvw5uMvz2UTKNhqYD-uRXBt7sAR_wcPtvBeAP6Q6i1A</recordid><startdate>20210105</startdate><enddate>20210105</enddate><creator>Liu, Dan</creator><creator>Liu, Jiale</creator><creator>Ma, Bing</creator><creator>Deng, Bo</creator><creator>Leng, Xigang</creator><creator>Kong, Deling</creator><creator>Liu, Lanxia</creator><general>Royal Society of Chemistry</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8153-9678</orcidid><orcidid>https://orcid.org/0000-0002-2961-9267</orcidid></search><sort><creationdate>20210105</creationdate><title>A simple self-adjuvanting biomimetic nanovaccine self-assembled with the conjugate of phospholipids and nucleotides can induce a strong cancer immunotherapeutic effect</title><author>Liu, Dan ; Liu, Jiale ; Ma, Bing ; Deng, Bo ; Leng, Xigang ; Kong, Deling ; Liu, Lanxia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-9821cb0ccfec4cb3e279c4c3883d5aa6cc00ce3123937c49205f1b78956475583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Antigens</topic><topic>Biomimetics</topic><topic>Conjugates</topic><topic>Controlled release</topic><topic>Cytokines</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Nanoparticles</topic><topic>Neoplasms - drug therapy</topic><topic>Nucleotides</topic><topic>Oligodeoxyribonucleotides</topic><topic>Phospholipids</topic><topic>Prolongation</topic><topic>Receptors</topic><topic>Self-assembly</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Dan</creatorcontrib><creatorcontrib>Liu, Jiale</creatorcontrib><creatorcontrib>Ma, Bing</creatorcontrib><creatorcontrib>Deng, Bo</creatorcontrib><creatorcontrib>Leng, Xigang</creatorcontrib><creatorcontrib>Kong, Deling</creatorcontrib><creatorcontrib>Liu, Lanxia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><jtitle>Biomaterials science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Dan</au><au>Liu, Jiale</au><au>Ma, Bing</au><au>Deng, Bo</au><au>Leng, Xigang</au><au>Kong, Deling</au><au>Liu, Lanxia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A simple self-adjuvanting biomimetic nanovaccine self-assembled with the conjugate of phospholipids and nucleotides can induce a strong cancer immunotherapeutic effect</atitle><jtitle>Biomaterials science</jtitle><addtitle>Biomater Sci</addtitle><date>2021-01-05</date><risdate>2021</risdate><volume>9</volume><issue>1</issue><spage>84</spage><epage>92</epage><pages>84-92</pages><issn>2047-4830</issn><eissn>2047-4849</eissn><abstract>Biomimetic nanoparticles have potential applications in many fields due to their favorable properties. Here, we developed a self-adjuvanting biomimetic anti-tumor nanovaccine, which was self-assembled with an amphiphilic conjugate synthesized with the phospholipids of 1,2-dioleoyl-
sn-glycero
-3-phosphoethanolamine (DOPE) and hydrophilic Toll-like receptor (TLR9) agonist CpG ODN. The nanovaccine could not only provide effective initial antigen stimulation and sustained long-term antigen supply with a controlled release, but also induce antigen cross-presentation
via
the MHC-I pathway initiating CD8
+
T-cell responses. Moreover, the dense nucleotide shell around the nanovaccine could promote antigen endocytosis
via
various receptor-mediated pathways into dendritic cells. CpG ODN interacted with TLR9 triggering the cytokine secretion of TNF-α and IL-10, which further boosted the anti-tumor humoral and cellular immune responses, which led to a significant tumor suppressive effect and remarkable survival prolongation. So, this nanovaccine self-assembled with phospholipid-nucleotide amphiphiles can serve as a safe, simple and efficient approach for anti-tumor immunotherapy.
The biomimetic nanovaccines not only promoted antigens endocytosis into dendritic cells
via
receptor-mediated pathways but also induced antigens cross-presentation eliciting CD8
+
T-cell responses. CPG-ODN as an adjuvant further enhanced the anti-tumor immune responses.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>33016303</pmid><doi>10.1039/d0bm01333a</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-8153-9678</orcidid><orcidid>https://orcid.org/0000-0002-2961-9267</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Royal Society Of Chemistry Journals 2008- |
subjects | Animals Antigens Biomimetics Conjugates Controlled release Cytokines Humans Immunotherapy Mice Mice, Inbred C57BL Nanoparticles Neoplasms - drug therapy Nucleotides Oligodeoxyribonucleotides Phospholipids Prolongation Receptors Self-assembly |
title | A simple self-adjuvanting biomimetic nanovaccine self-assembled with the conjugate of phospholipids and nucleotides can induce a strong cancer immunotherapeutic effect |
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