Microneedle and mucosal delivery of influenza vaccines

被引:1
|
作者
Kang, Sang-Moo [1 ,2 ]
Song, Jae-Min [1 ,2 ,3 ]
Kim, Yeu-Chun [4 ]
机构
[1] Georgia State Univ, Ctr Inflammat Immun & Infect, Atlanta, GA 30303 USA
[2] Georgia State Univ, Dept Biol, Atlanta, GA 30303 USA
[3] Sungshin Womens Univ, Dept Global Med Sci, Seoul, South Korea
[4] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Taejon 305701, South Korea
关键词
influenza vaccine; microneedles; mucosal immunization; skin vaccination; VIRUS-LIKE PARTICLES; EPIDERMAL POWDER IMMUNIZATION; HUMAN SKIN EXPLANTS; HEAT-LABILE TOXIN; ANTIBODY-RESPONSES; TRANSCUTANEOUS IMMUNIZATION; IMMUNE-RESPONSES; INTRADERMAL DELIVERY; SEASONAL INFLUENZA; CROSS-PROTECTION;
D O I
10.1586/ERV.12.25
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In recent years with the threat of pandemic influenza and other public health needs, alternative vaccination methods other than intramuscular immunization have received great attention. The skin and mucosal surfaces are attractive sites probably because of both noninvasive access to the vaccine delivery and unique immunological responses. Intradermal vaccines using a microinjection system (BD Soluvia (TM)) and intranasal vaccines (FluMist (R)) are licensed. As a new vaccination method, solid microneedles have been developed using a simple device that may be suitable for self-administration. Because coated microneedle influenza vaccines are administered in the solid state, developing formulations maintaining the stability of influenza vaccines is an important issue to be considered. Marketable microneedle devices and clinical trials remain to be developed. Other alternative mucosal routes such as oral and intranasal delivery systems are also attractive for inducing cross-protective mucosal immunity, but effective non-live mucosal vaccines remain to be developed.
引用
收藏
页码:547 / 560
页数:14
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