Oral mucosal vaccination using integrated fiber microneedles
The oral mucosa is an attractive site for immunization due to its accessibility and ability to elicit local and systemic immune responses. However, evaluating oral mucosal immunogenicity has proven challenging due to the physical barriers and immunological complexity of the oral mucosa. Microneedles...
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Veröffentlicht in: | Journal of controlled release 2024-03, Vol.367, p.649-660 |
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creator | Creighton, Rachel L. Faber, Kate A. Tobos, Carmen I. Doan, My-Anh Guo, Teri Woodrow, Kim A. |
description | The oral mucosa is an attractive site for immunization due to its accessibility and ability to elicit local and systemic immune responses. However, evaluating oral mucosal immunogenicity has proven challenging due to the physical barriers and immunological complexity of the oral mucosa. Microneedles can overcome these physical barriers, but previous work has been limited in the scope of microneedle delivery site, geometry, and release kinetics, all of which are expected to affect physiological responses. Here, we develop integrated fiber microneedle devices, an oral dosage form with tunable geometries and material configurations capable of both burst and sustained release to controlled depths in the oral mucosa. Integrated fiber microneedles administered to either the buccal or sublingual mucosa result in seroconversion and antigen-specific interferon-γ secretion in splenocytes. The dynamics and magnitude of the resulting immune response can be modulated by tuning microneedle release kinetics. Optimal microneedle geometry is site-specific, with longer microneedles eliciting greater immunogenicity in the buccal mucosa, and shorter microneedles eliciting greater immunogenicity in the sublingual mucosa. The Th1/Th2 phenotype of the resulting immune response is also dependent on integrated fiber microneedle length. Together, these results establish integrated fiber microneedles as a multifunctional delivery system for the oral mucosa and motivate further exploration using tunable delivery systems to better understand oral mucosal immunity.
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•Integrated fiber microneedles (iFMD) have tunable geometries and release kinetics.•iFMDs are immunogenic when delivered to either the buccal or sublingual mucosa.•Antigen delivery from the fiber and backfill elicit the most robust immune response.•Optimal microneedle geometry is site-specific.•Longer iFMDs result in a more Th-1 biased immune response in the buccal mucosa. |
doi_str_mv | 10.1016/j.jconrel.2024.01.062 |
format | Article |
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[Display omitted]
•Integrated fiber microneedles (iFMD) have tunable geometries and release kinetics.•iFMDs are immunogenic when delivered to either the buccal or sublingual mucosa.•Antigen delivery from the fiber and backfill elicit the most robust immune response.•Optimal microneedle geometry is site-specific.•Longer iFMDs result in a more Th-1 biased immune response in the buccal mucosa.</description><identifier>ISSN: 0168-3659</identifier><identifier>EISSN: 1873-4995</identifier><identifier>DOI: 10.1016/j.jconrel.2024.01.062</identifier><identifier>PMID: 38295993</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Administration, Cutaneous ; Antigens ; dosage forms ; Drug Delivery Systems ; Electrospun fibers ; geometry ; immune response ; Immunity, Mucosal ; immunogenicity ; Microneedle ; Mouth Mucosa ; mucosa ; mucosal immunity ; Mucosal immunization ; Needles ; oral administration ; Oral mucosal delivery ; Ovalbumin ; phenotype ; secretion ; seroconversion ; splenocytes ; vaccination ; Vaccination - methods ; Vaccine</subject><ispartof>Journal of controlled release, 2024-03, Vol.367, p.649-660</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c346t-768bc17d5c28a2a4827db1d652a1bfb7f666d05c4cddb690a3cffec01b8084f83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0168365924000774$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38295993$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Creighton, Rachel L.</creatorcontrib><creatorcontrib>Faber, Kate A.</creatorcontrib><creatorcontrib>Tobos, Carmen I.</creatorcontrib><creatorcontrib>Doan, My-Anh</creatorcontrib><creatorcontrib>Guo, Teri</creatorcontrib><creatorcontrib>Woodrow, Kim A.</creatorcontrib><title>Oral mucosal vaccination using integrated fiber microneedles</title><title>Journal of controlled release</title><addtitle>J Control Release</addtitle><description>The oral mucosa is an attractive site for immunization due to its accessibility and ability to elicit local and systemic immune responses. However, evaluating oral mucosal immunogenicity has proven challenging due to the physical barriers and immunological complexity of the oral mucosa. Microneedles can overcome these physical barriers, but previous work has been limited in the scope of microneedle delivery site, geometry, and release kinetics, all of which are expected to affect physiological responses. Here, we develop integrated fiber microneedle devices, an oral dosage form with tunable geometries and material configurations capable of both burst and sustained release to controlled depths in the oral mucosa. Integrated fiber microneedles administered to either the buccal or sublingual mucosa result in seroconversion and antigen-specific interferon-γ secretion in splenocytes. The dynamics and magnitude of the resulting immune response can be modulated by tuning microneedle release kinetics. Optimal microneedle geometry is site-specific, with longer microneedles eliciting greater immunogenicity in the buccal mucosa, and shorter microneedles eliciting greater immunogenicity in the sublingual mucosa. The Th1/Th2 phenotype of the resulting immune response is also dependent on integrated fiber microneedle length. Together, these results establish integrated fiber microneedles as a multifunctional delivery system for the oral mucosa and motivate further exploration using tunable delivery systems to better understand oral mucosal immunity.
[Display omitted]
•Integrated fiber microneedles (iFMD) have tunable geometries and release kinetics.•iFMDs are immunogenic when delivered to either the buccal or sublingual mucosa.•Antigen delivery from the fiber and backfill elicit the most robust immune response.•Optimal microneedle geometry is site-specific.•Longer iFMDs result in a more Th-1 biased immune response in the buccal mucosa.</description><subject>Administration, Cutaneous</subject><subject>Antigens</subject><subject>dosage forms</subject><subject>Drug Delivery Systems</subject><subject>Electrospun fibers</subject><subject>geometry</subject><subject>immune response</subject><subject>Immunity, Mucosal</subject><subject>immunogenicity</subject><subject>Microneedle</subject><subject>Mouth Mucosa</subject><subject>mucosa</subject><subject>mucosal immunity</subject><subject>Mucosal immunization</subject><subject>Needles</subject><subject>oral administration</subject><subject>Oral mucosal delivery</subject><subject>Ovalbumin</subject><subject>phenotype</subject><subject>secretion</subject><subject>seroconversion</subject><subject>splenocytes</subject><subject>vaccination</subject><subject>Vaccination - methods</subject><subject>Vaccine</subject><issn>0168-3659</issn><issn>1873-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLxDAUhYMozvj4CUqXblrzbgKCyOALBDe6DmlyKyl9jEk74L-3w4xuZ3U237mH-yF0RXBBMJG3TdG4oY_QFhRTXmBSYEmP0JKokuVca3GMljOnciaFXqCzlBqMsWC8PEULpqgWWrMlunuPts26yQ1pzo11LvR2DEOfTSn0X1noR_iKdgSf1aGCmHXBxaEH8C2kC3RS2zbB5T7P0efT48fqJX97f35dPbzljnE55qVUlSOlF44qSy1XtPQV8VJQS6q6KmsppcfCced9JTW2zNU1OEwqhRWvFTtHN7u76zh8T5BG04XkoG1tD8OUDCOCEc2x5gdRqqngSpSczajYofNDKUWozTqGzsYfQ7DZOjaN2Ts2W8cGEzM7nnvX-4mp6sD_t_6kzsD9DoDZySZANMkF6B34EMGNxg_hwMQvsHuQNw</recordid><startdate>202403</startdate><enddate>202403</enddate><creator>Creighton, Rachel L.</creator><creator>Faber, Kate A.</creator><creator>Tobos, Carmen I.</creator><creator>Doan, My-Anh</creator><creator>Guo, Teri</creator><creator>Woodrow, Kim A.</creator><general>Elsevier B.V</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>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>202403</creationdate><title>Oral mucosal vaccination using integrated fiber microneedles</title><author>Creighton, Rachel L. ; Faber, Kate A. ; Tobos, Carmen I. ; Doan, My-Anh ; Guo, Teri ; Woodrow, Kim A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c346t-768bc17d5c28a2a4827db1d652a1bfb7f666d05c4cddb690a3cffec01b8084f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Administration, Cutaneous</topic><topic>Antigens</topic><topic>dosage forms</topic><topic>Drug Delivery Systems</topic><topic>Electrospun fibers</topic><topic>geometry</topic><topic>immune response</topic><topic>Immunity, Mucosal</topic><topic>immunogenicity</topic><topic>Microneedle</topic><topic>Mouth Mucosa</topic><topic>mucosa</topic><topic>mucosal immunity</topic><topic>Mucosal immunization</topic><topic>Needles</topic><topic>oral administration</topic><topic>Oral mucosal delivery</topic><topic>Ovalbumin</topic><topic>phenotype</topic><topic>secretion</topic><topic>seroconversion</topic><topic>splenocytes</topic><topic>vaccination</topic><topic>Vaccination - methods</topic><topic>Vaccine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Creighton, Rachel L.</creatorcontrib><creatorcontrib>Faber, Kate A.</creatorcontrib><creatorcontrib>Tobos, Carmen I.</creatorcontrib><creatorcontrib>Doan, My-Anh</creatorcontrib><creatorcontrib>Guo, Teri</creatorcontrib><creatorcontrib>Woodrow, Kim A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Journal of controlled release</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Creighton, Rachel L.</au><au>Faber, Kate A.</au><au>Tobos, Carmen I.</au><au>Doan, My-Anh</au><au>Guo, Teri</au><au>Woodrow, Kim A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral mucosal vaccination using integrated fiber microneedles</atitle><jtitle>Journal of controlled release</jtitle><addtitle>J Control Release</addtitle><date>2024-03</date><risdate>2024</risdate><volume>367</volume><spage>649</spage><epage>660</epage><pages>649-660</pages><issn>0168-3659</issn><eissn>1873-4995</eissn><abstract>The oral mucosa is an attractive site for immunization due to its accessibility and ability to elicit local and systemic immune responses. However, evaluating oral mucosal immunogenicity has proven challenging due to the physical barriers and immunological complexity of the oral mucosa. Microneedles can overcome these physical barriers, but previous work has been limited in the scope of microneedle delivery site, geometry, and release kinetics, all of which are expected to affect physiological responses. Here, we develop integrated fiber microneedle devices, an oral dosage form with tunable geometries and material configurations capable of both burst and sustained release to controlled depths in the oral mucosa. Integrated fiber microneedles administered to either the buccal or sublingual mucosa result in seroconversion and antigen-specific interferon-γ secretion in splenocytes. The dynamics and magnitude of the resulting immune response can be modulated by tuning microneedle release kinetics. Optimal microneedle geometry is site-specific, with longer microneedles eliciting greater immunogenicity in the buccal mucosa, and shorter microneedles eliciting greater immunogenicity in the sublingual mucosa. The Th1/Th2 phenotype of the resulting immune response is also dependent on integrated fiber microneedle length. Together, these results establish integrated fiber microneedles as a multifunctional delivery system for the oral mucosa and motivate further exploration using tunable delivery systems to better understand oral mucosal immunity.
[Display omitted]
•Integrated fiber microneedles (iFMD) have tunable geometries and release kinetics.•iFMDs are immunogenic when delivered to either the buccal or sublingual mucosa.•Antigen delivery from the fiber and backfill elicit the most robust immune response.•Optimal microneedle geometry is site-specific.•Longer iFMDs result in a more Th-1 biased immune response in the buccal mucosa.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38295993</pmid><doi>10.1016/j.jconrel.2024.01.062</doi><tpages>12</tpages></addata></record> |
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subjects | Administration, Cutaneous Antigens dosage forms Drug Delivery Systems Electrospun fibers geometry immune response Immunity, Mucosal immunogenicity Microneedle Mouth Mucosa mucosa mucosal immunity Mucosal immunization Needles oral administration Oral mucosal delivery Ovalbumin phenotype secretion seroconversion splenocytes vaccination Vaccination - methods Vaccine |
title | Oral mucosal vaccination using integrated fiber microneedles |
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