Enzyme-Catalyzed Formation of Supramolecular Hydrogels as Promising Vaccine Adjuvants
Promising vaccine adjuvants of self‐assembling peptide hydrogels for protein ovalbumin (OVA) are introduced in this study. The hydrogels are formed by the enzyme of phosphatase, and the vaccine adjuvant potency of both l‐ and d‐peptide hydrogels is evaluated. The results indicate that, compared with...
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Veröffentlicht in: | Advanced functional materials 2016-03, Vol.26 (11), p.1822-1829 |
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container_title | Advanced functional materials |
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creator | Wang, Huaimin Luo, Zichao Wang, Youzhi He, Tao Yang, Chengbiao Ren, Chunhua Ma, Linsha Gong, Changyang Li, Xingyi Yang, Zhimou |
description | Promising vaccine adjuvants of self‐assembling peptide hydrogels for protein ovalbumin (OVA) are introduced in this study. The hydrogels are formed by the enzyme of phosphatase, and the vaccine adjuvant potency of both l‐ and d‐peptide hydrogels is evaluated. The results indicate that, compared with the clinically used alum adjuvant, both l‐ and d‐peptide hydrogels can increase the IgG production of OVA for about 1.3 and 3.8 times, respectively. Both gels can enhance antigen uptake and induce dendritic cell maturation, and promote and prolong accumulation of antigen in lymph node, as well as evoke germinal center formation. However, the d‐peptide hydrogel with OVA exhibits a slightly more efficient accumulation of OVA in the lymph nodes and seems preventing tumor growth more significantly than its l‐counterpart. With the good biocompatibility and degradability of peptide hydrogels, the hydrogels described in this study have big potential for the production of protein vaccines for immunotherapy against different diseases.
Short peptides and the protein antigen can coassemble into supramolecular hydrogels capable of raising both humoral and cellular immune responses in mice. |
doi_str_mv | 10.1002/adfm.201505188 |
format | Article |
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Short peptides and the protein antigen can coassemble into supramolecular hydrogels capable of raising both humoral and cellular immune responses in mice.</description><identifier>ISSN: 1616-301X</identifier><identifier>EISSN: 1616-3028</identifier><identifier>DOI: 10.1002/adfm.201505188</identifier><language>eng</language><publisher>Blackwell Publishing Ltd</publisher><subject>adjuvant ; Adjuvants ; Antigens ; Formations ; Hydrogels ; Lymph ; Peptides ; Proteins ; self-assembly ; supramolecular hydrogel ; vaccine ; Vaccines</subject><ispartof>Advanced functional materials, 2016-03, Vol.26 (11), p.1822-1829</ispartof><rights>2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4638-efd9a9962d534019d091f330b7b3f021bb91e6b96a90b15d011153c2ba955a873</citedby><cites>FETCH-LOGICAL-c4638-efd9a9962d534019d091f330b7b3f021bb91e6b96a90b15d011153c2ba955a873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fadfm.201505188$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fadfm.201505188$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Wang, Huaimin</creatorcontrib><creatorcontrib>Luo, Zichao</creatorcontrib><creatorcontrib>Wang, Youzhi</creatorcontrib><creatorcontrib>He, Tao</creatorcontrib><creatorcontrib>Yang, Chengbiao</creatorcontrib><creatorcontrib>Ren, Chunhua</creatorcontrib><creatorcontrib>Ma, Linsha</creatorcontrib><creatorcontrib>Gong, Changyang</creatorcontrib><creatorcontrib>Li, Xingyi</creatorcontrib><creatorcontrib>Yang, Zhimou</creatorcontrib><title>Enzyme-Catalyzed Formation of Supramolecular Hydrogels as Promising Vaccine Adjuvants</title><title>Advanced functional materials</title><addtitle>Adv. Funct. Mater</addtitle><description>Promising vaccine adjuvants of self‐assembling peptide hydrogels for protein ovalbumin (OVA) are introduced in this study. The hydrogels are formed by the enzyme of phosphatase, and the vaccine adjuvant potency of both l‐ and d‐peptide hydrogels is evaluated. The results indicate that, compared with the clinically used alum adjuvant, both l‐ and d‐peptide hydrogels can increase the IgG production of OVA for about 1.3 and 3.8 times, respectively. Both gels can enhance antigen uptake and induce dendritic cell maturation, and promote and prolong accumulation of antigen in lymph node, as well as evoke germinal center formation. However, the d‐peptide hydrogel with OVA exhibits a slightly more efficient accumulation of OVA in the lymph nodes and seems preventing tumor growth more significantly than its l‐counterpart. With the good biocompatibility and degradability of peptide hydrogels, the hydrogels described in this study have big potential for the production of protein vaccines for immunotherapy against different diseases.
Short peptides and the protein antigen can coassemble into supramolecular hydrogels capable of raising both humoral and cellular immune responses in mice.</description><subject>adjuvant</subject><subject>Adjuvants</subject><subject>Antigens</subject><subject>Formations</subject><subject>Hydrogels</subject><subject>Lymph</subject><subject>Peptides</subject><subject>Proteins</subject><subject>self-assembly</subject><subject>supramolecular hydrogel</subject><subject>vaccine</subject><subject>Vaccines</subject><issn>1616-301X</issn><issn>1616-3028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPg0AQgInRxOfVM0cv1BmWBfbYVGlN6is-6m0zwGJQYOsuqPTX2wbTePM0c_i-yeRznFOEEQL455QX9cgH5MAxjnecAwwx9Bj48e52x5d959DaNwCMIhYcOE-XzaqvlTehlqp-pXI30aamttSNqwv3oVsaqnWlsq4i48763OhXVVmXrHtndF3asnl1nynLyka54_yt-6SmtcfOXkGVVSe_88h5Si4fJzNvfju9moznXhaELPZUkQsSIvRzzgJAkYPAgjFIo5QV4GOaClRhKkISkCLPARE5y_yUBOcUR-zIORvuLo3-6JRt5fqjTFUVNUp3VmIMwIEFPq7R0YBmRltrVCGXpqzJ9BJBbvrJTT-57bcWxCB8lZXq_6Hl-CK5_ut6g1vaVn1vXTLvMoxYxOXiZirn94vJhbhJ5IL9ACl1g9E</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Wang, Huaimin</creator><creator>Luo, Zichao</creator><creator>Wang, Youzhi</creator><creator>He, Tao</creator><creator>Yang, Chengbiao</creator><creator>Ren, Chunhua</creator><creator>Ma, Linsha</creator><creator>Gong, Changyang</creator><creator>Li, Xingyi</creator><creator>Yang, Zhimou</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20160301</creationdate><title>Enzyme-Catalyzed Formation of Supramolecular Hydrogels as Promising Vaccine Adjuvants</title><author>Wang, Huaimin ; Luo, Zichao ; Wang, Youzhi ; He, Tao ; Yang, Chengbiao ; Ren, Chunhua ; Ma, Linsha ; Gong, Changyang ; Li, Xingyi ; Yang, Zhimou</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4638-efd9a9962d534019d091f330b7b3f021bb91e6b96a90b15d011153c2ba955a873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>adjuvant</topic><topic>Adjuvants</topic><topic>Antigens</topic><topic>Formations</topic><topic>Hydrogels</topic><topic>Lymph</topic><topic>Peptides</topic><topic>Proteins</topic><topic>self-assembly</topic><topic>supramolecular hydrogel</topic><topic>vaccine</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Huaimin</creatorcontrib><creatorcontrib>Luo, Zichao</creatorcontrib><creatorcontrib>Wang, Youzhi</creatorcontrib><creatorcontrib>He, Tao</creatorcontrib><creatorcontrib>Yang, Chengbiao</creatorcontrib><creatorcontrib>Ren, Chunhua</creatorcontrib><creatorcontrib>Ma, Linsha</creatorcontrib><creatorcontrib>Gong, Changyang</creatorcontrib><creatorcontrib>Li, Xingyi</creatorcontrib><creatorcontrib>Yang, Zhimou</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Advanced functional materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Huaimin</au><au>Luo, Zichao</au><au>Wang, Youzhi</au><au>He, Tao</au><au>Yang, Chengbiao</au><au>Ren, Chunhua</au><au>Ma, Linsha</au><au>Gong, Changyang</au><au>Li, Xingyi</au><au>Yang, Zhimou</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enzyme-Catalyzed Formation of Supramolecular Hydrogels as Promising Vaccine Adjuvants</atitle><jtitle>Advanced functional materials</jtitle><addtitle>Adv. Funct. Mater</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>26</volume><issue>11</issue><spage>1822</spage><epage>1829</epage><pages>1822-1829</pages><issn>1616-301X</issn><eissn>1616-3028</eissn><abstract>Promising vaccine adjuvants of self‐assembling peptide hydrogels for protein ovalbumin (OVA) are introduced in this study. The hydrogels are formed by the enzyme of phosphatase, and the vaccine adjuvant potency of both l‐ and d‐peptide hydrogels is evaluated. The results indicate that, compared with the clinically used alum adjuvant, both l‐ and d‐peptide hydrogels can increase the IgG production of OVA for about 1.3 and 3.8 times, respectively. Both gels can enhance antigen uptake and induce dendritic cell maturation, and promote and prolong accumulation of antigen in lymph node, as well as evoke germinal center formation. However, the d‐peptide hydrogel with OVA exhibits a slightly more efficient accumulation of OVA in the lymph nodes and seems preventing tumor growth more significantly than its l‐counterpart. With the good biocompatibility and degradability of peptide hydrogels, the hydrogels described in this study have big potential for the production of protein vaccines for immunotherapy against different diseases.
Short peptides and the protein antigen can coassemble into supramolecular hydrogels capable of raising both humoral and cellular immune responses in mice.</abstract><pub>Blackwell Publishing Ltd</pub><doi>10.1002/adfm.201505188</doi><tpages>8</tpages></addata></record> |
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subjects | adjuvant Adjuvants Antigens Formations Hydrogels Lymph Peptides Proteins self-assembly supramolecular hydrogel vaccine Vaccines |
title | Enzyme-Catalyzed Formation of Supramolecular Hydrogels as Promising Vaccine Adjuvants |
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