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Intradermal vaccination with a phytoglycogen nanoparticle and STING agonist induces cytotoxic T lymphocyte-mediated antitumor immunity
A critical aspect of cancer vaccine development is the formulation with effective adjuvants. This study evaluated whether combining a cationic plant-derived nanoparticle adjuvant (Nano-11) with the clinically tested STING agonist ADU-S100 (MIW815) could stimulate anticancer immunity by intradermal v...
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Published in: | npj vaccines 2024-08, Vol.9 (1), p.149-15 |
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description | A critical aspect of cancer vaccine development is the formulation with effective adjuvants. This study evaluated whether combining a cationic plant-derived nanoparticle adjuvant (Nano-11) with the clinically tested STING agonist ADU-S100 (MIW815) could stimulate anticancer immunity by intradermal vaccination. Nano-11 combined with ADU-S100 (NanoST) synergistically activated antigen-presenting cells, facilitating protein antigen cross-presentation in vitro and in vivo. Intradermal vaccination using ovalbumin (OVA) as a tumor antigen and combined with Nano-11 or NanoST prevented the development of murine B16-OVA melanoma and E.G7-OVA lymphoma tumors. The antitumor immunity was abolished by CD8
+
T cell depletion but not by CD4
+
T cell depletion. Therapeutic vaccination with NanoST increased mouse survival by inhibiting B16-OVA tumor growth, and this effect was further enhanced by PD-1 checkpoint blockade. Our study provides a strong rationale for developing NanoST as an adjuvant for intradermal vaccination and next-generation preventative and therapeutic cancer vaccines by STING-targeted activation. |
doi_str_mv | 10.1038/s41541-024-00943-8 |
format | article |
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+
T cell depletion but not by CD4
+
T cell depletion. Therapeutic vaccination with NanoST increased mouse survival by inhibiting B16-OVA tumor growth, and this effect was further enhanced by PD-1 checkpoint blockade. Our study provides a strong rationale for developing NanoST as an adjuvant for intradermal vaccination and next-generation preventative and therapeutic cancer vaccines by STING-targeted activation.</description><identifier>ISSN: 2059-0105</identifier><identifier>EISSN: 2059-0105</identifier><identifier>DOI: 10.1038/s41541-024-00943-8</identifier><identifier>PMID: 39152131</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/250/590/2291 ; 631/67/2195 ; Adjuvants ; Antigens ; Biomedical and Life Sciences ; Biomedicine ; Cancer vaccines ; Cytotoxicity ; Immunity (Disease) ; Immunotherapy ; Infectious Diseases ; Kinases ; Lymphocytes ; Lymphoma ; Medical Microbiology ; Medical research ; Melanoma ; Nanoparticles ; Proteins ; Public Health ; Tumors ; Vaccine ; Vaccines ; Virology</subject><ispartof>npj vaccines, 2024-08, Vol.9 (1), p.149-15</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-d323t-418af44fd821528dbf435ba83bff60e95ab645057208826d42f34d5bddf04e2b3</cites><orcidid>0000-0001-5397-3162 ; 0000-0002-0798-4132</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/3093693607?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39152131$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hernandez-Franco, Juan F.</creatorcontrib><creatorcontrib>Jan, Imran M.</creatorcontrib><creatorcontrib>Elzey, Bennett D.</creatorcontrib><creatorcontrib>HogenEsch, Harm</creatorcontrib><title>Intradermal vaccination with a phytoglycogen nanoparticle and STING agonist induces cytotoxic T lymphocyte-mediated antitumor immunity</title><title>npj vaccines</title><addtitle>npj Vaccines</addtitle><addtitle>NPJ Vaccines</addtitle><description>A critical aspect of cancer vaccine development is the formulation with effective adjuvants. This study evaluated whether combining a cationic plant-derived nanoparticle adjuvant (Nano-11) with the clinically tested STING agonist ADU-S100 (MIW815) could stimulate anticancer immunity by intradermal vaccination. Nano-11 combined with ADU-S100 (NanoST) synergistically activated antigen-presenting cells, facilitating protein antigen cross-presentation in vitro and in vivo. Intradermal vaccination using ovalbumin (OVA) as a tumor antigen and combined with Nano-11 or NanoST prevented the development of murine B16-OVA melanoma and E.G7-OVA lymphoma tumors. The antitumor immunity was abolished by CD8
+
T cell depletion but not by CD4
+
T cell depletion. Therapeutic vaccination with NanoST increased mouse survival by inhibiting B16-OVA tumor growth, and this effect was further enhanced by PD-1 checkpoint blockade. Our study provides a strong rationale for developing NanoST as an adjuvant for intradermal vaccination and next-generation preventative and therapeutic cancer vaccines by STING-targeted activation.</description><subject>631/250/590/2291</subject><subject>631/67/2195</subject><subject>Adjuvants</subject><subject>Antigens</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer vaccines</subject><subject>Cytotoxicity</subject><subject>Immunity (Disease)</subject><subject>Immunotherapy</subject><subject>Infectious Diseases</subject><subject>Kinases</subject><subject>Lymphocytes</subject><subject>Lymphoma</subject><subject>Medical Microbiology</subject><subject>Medical research</subject><subject>Melanoma</subject><subject>Nanoparticles</subject><subject>Proteins</subject><subject>Public Health</subject><subject>Tumors</subject><subject>Vaccine</subject><subject>Vaccines</subject><subject>Virology</subject><issn>2059-0105</issn><issn>2059-0105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdks1u1DAUhSMEolXpC7BAltiwSbn-S5wlqqCMVJUFw9pybCfjUWIPtgPkBXhuPJ3hR6xsXX_36B7fU1UvMdxgoOJtYpgzXANhNUDHaC2eVJcEeFcDBv70n_tFdZ3SHgBw21DewvPqgnaYE0zxZfVz43NUxsZZTeib0tp5lV3w6LvLO6TQYbfmME6rDqP1yCsfDipmpyeLlDfo83bzcIfUGLxLGTlvFm0T0qUnhx9Ooy2a1vmwC6Vi69kap7I1pTO7vMwhIjfPi3d5fVE9G9SU7PX5vKq-fHi_vf1Y33-629y-u68NJTTXDAs1MDYYQYoBYfqBUd4rQfthaMB2XPUN48BbAkKQxjAyUGZ4b8wAzJKeXlWbk64Jai8P0c0qrjIoJx8LIY7ybE_qoe80b5uWioYxRnvClOoE5dB0glBdtN6ctA4xfF1synJ2SdtpUt6GJUla1gKlsekK-vo_dB-W6IvTI3UkGmgL9epMLX35qz_j_d5WAegJSOXJjzb-lcEgj7GQp1jIEgv5GAsp6C8FuqjS</recordid><startdate>20240817</startdate><enddate>20240817</enddate><creator>Hernandez-Franco, Juan F.</creator><creator>Jan, Imran M.</creator><creator>Elzey, Bennett D.</creator><creator>HogenEsch, Harm</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><general>Nature Portfolio</general><scope>C6C</scope><scope>NPM</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-5397-3162</orcidid><orcidid>https://orcid.org/0000-0002-0798-4132</orcidid></search><sort><creationdate>20240817</creationdate><title>Intradermal vaccination with a phytoglycogen nanoparticle and STING agonist induces cytotoxic T lymphocyte-mediated antitumor immunity</title><author>Hernandez-Franco, Juan F. ; Jan, Imran M. ; Elzey, Bennett D. ; HogenEsch, Harm</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-d323t-418af44fd821528dbf435ba83bff60e95ab645057208826d42f34d5bddf04e2b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>631/250/590/2291</topic><topic>631/67/2195</topic><topic>Adjuvants</topic><topic>Antigens</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer vaccines</topic><topic>Cytotoxicity</topic><topic>Immunity (Disease)</topic><topic>Immunotherapy</topic><topic>Infectious Diseases</topic><topic>Kinases</topic><topic>Lymphocytes</topic><topic>Lymphoma</topic><topic>Medical Microbiology</topic><topic>Medical research</topic><topic>Melanoma</topic><topic>Nanoparticles</topic><topic>Proteins</topic><topic>Public Health</topic><topic>Tumors</topic><topic>Vaccine</topic><topic>Vaccines</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hernandez-Franco, Juan F.</creatorcontrib><creatorcontrib>Jan, Imran M.</creatorcontrib><creatorcontrib>Elzey, Bennett D.</creatorcontrib><creatorcontrib>HogenEsch, Harm</creatorcontrib><collection>SpringerOpen</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Health & Medical Complete (ProQuest Database)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Family Health</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Healthcare Administration Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Directory of Open Access Journals</collection><jtitle>npj vaccines</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hernandez-Franco, Juan F.</au><au>Jan, Imran M.</au><au>Elzey, Bennett D.</au><au>HogenEsch, Harm</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intradermal vaccination with a phytoglycogen nanoparticle and STING agonist induces cytotoxic T lymphocyte-mediated antitumor immunity</atitle><jtitle>npj vaccines</jtitle><stitle>npj Vaccines</stitle><addtitle>NPJ Vaccines</addtitle><date>2024-08-17</date><risdate>2024</risdate><volume>9</volume><issue>1</issue><spage>149</spage><epage>15</epage><pages>149-15</pages><issn>2059-0105</issn><eissn>2059-0105</eissn><abstract>A critical aspect of cancer vaccine development is the formulation with effective adjuvants. This study evaluated whether combining a cationic plant-derived nanoparticle adjuvant (Nano-11) with the clinically tested STING agonist ADU-S100 (MIW815) could stimulate anticancer immunity by intradermal vaccination. Nano-11 combined with ADU-S100 (NanoST) synergistically activated antigen-presenting cells, facilitating protein antigen cross-presentation in vitro and in vivo. Intradermal vaccination using ovalbumin (OVA) as a tumor antigen and combined with Nano-11 or NanoST prevented the development of murine B16-OVA melanoma and E.G7-OVA lymphoma tumors. The antitumor immunity was abolished by CD8
+
T cell depletion but not by CD4
+
T cell depletion. Therapeutic vaccination with NanoST increased mouse survival by inhibiting B16-OVA tumor growth, and this effect was further enhanced by PD-1 checkpoint blockade. Our study provides a strong rationale for developing NanoST as an adjuvant for intradermal vaccination and next-generation preventative and therapeutic cancer vaccines by STING-targeted activation.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>39152131</pmid><doi>10.1038/s41541-024-00943-8</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0001-5397-3162</orcidid><orcidid>https://orcid.org/0000-0002-0798-4132</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/250/590/2291 631/67/2195 Adjuvants Antigens Biomedical and Life Sciences Biomedicine Cancer vaccines Cytotoxicity Immunity (Disease) Immunotherapy Infectious Diseases Kinases Lymphocytes Lymphoma Medical Microbiology Medical research Melanoma Nanoparticles Proteins Public Health Tumors Vaccine Vaccines Virology |
title | Intradermal vaccination with a phytoglycogen nanoparticle and STING agonist induces cytotoxic T lymphocyte-mediated antitumor immunity |
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