Noninvasive Transdermal Vaccination Using Hyaluronan Nanocarriers and Laser Adjuvant

被引:54
作者
Kim, Ki Su [1 ,2 ]
Kim, Hyemin [3 ]
Park, Yunji [4 ]
Kong, Won Ho [3 ]
Lee, Seung Woo [4 ,5 ]
Kwok, Sheldon J. J. [1 ,2 ]
Hahn, Sei Kwang [1 ,2 ,3 ]
Yun, Seok Hyun [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Wellman Ctr Photomed, 65 Landsdowne St,UP-5, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Med, Dept Dermatol, 40 Blossom St, Boston, MA 02140 USA
[3] Pohang Univ Sci & Technol POSTECH, Dept Mat Sci & Engn, 77 Cheongam Ro, Pohang 790784, Gyeongbuk, South Korea
[4] POSTECH, Div Integrat Biosci & Biotechnol, 77 Cheongam Ro, Pohang 790784, Gyeongbuk, South Korea
[5] POSTECH, Dept Life Sci, 77 Cheongam Ro, Pohang 790784, Gyeongbuk, South Korea
基金
新加坡国家研究基金会; 美国国家卫生研究院;
关键词
DERMAL DENDRITIC CELLS; TRANSCUTANEOUS DRUG; IMMUNE-SYSTEM; NEEDLE PHOBIA; DELIVERY; SKIN; IMMUNIZATION; ACID; VACCINES; OLIGOSACCHARIDES;
D O I
10.1002/adfm.201504879
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Vaccines are commonly administered by injection using needles. Although transdermal microneedles are less invasive promising alternatives, needle-free topical vaccination without involving physical damage to the natural skin barrier is still sought after as it can further reduce needle-induced anxiety and is simple to administer. However, this long-standing goal has been elusive since the intact skin is impermeable to most macromolecules. Here, we show an efficient, noninvasive transdermal vaccination by employing two key innovations: the use of hyaluronan (HA) as vaccine carriers and non-ablative laser adjuvants. Conjugates of a model vaccine ovalbumin (OVA) and HAHA-OVA conjugates-induced more effective maturation of dendritic cells in vitro, compared to OVA. Following topical administration in the skin, HA-OVA conjugates penetrated into the epidermis and dermis in murine and porcine skins, as revealed by intravital microscopy and fluorescence assay. Topical administration of HA-OVA conjugates significantly elevated both humoral and mucosal antibodies, with peak levels at four weeks. An OVA challenge at week eight elicited strong immune-recall responses. With pretreatment of the skin using non-ablative fractional laser beams as adjuvant, strong immunization was achieved with much reduced doses of HA-OVA (1 mg kg(-1) OVA). Our results demonstrate the potential of the noninvasive patch-type transdermal vaccination platform.
引用
收藏
页码:2512 / 2522
页数:11
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