Influenza is a major cause of morbidity and mortality worldwide. Although vaccination is the most effective Strategy to prevent infection, influenza vaccination coverage is insufficient and improved vaccine immunogenicity is needed. We propose development of a microneedle patch that is simple enough to increase vaccination coverage by enabling self-administration and specifically designed to improve immunogenicity by targeting dendritic cells in skin. Microneedles (MN) are micron-scale, solid needles that administer vaccine directly into skin using a simple, painless and minimally invasive approach. The patch is designed to enable skin vaccination with a patch application time of just seconds, generation of no sharp biohazardous waste, and antigen stability during storage without refrigeration. The goal of this milestone-driven project is to develop a MN patch for influenza vaccination and assess its safety and immunogenicity in a Phase I clinical trial.
In Aim 1, based at Georgia Tech, we will design, formulate, and fabricate MN for simple, rapid application and long-term stability.
In Aim 2, based at Emory, we will assess MN vaccination in three animal models with the goals of validating suitability for human trials and enhancing immunogenicity.
Aim 3 will be achieved with external contractors and consultants to develop and validate cGMP manufacturing, conduct GLP preclinical studies and obtain an IND. This work will culminate in a Phase I clinical trial carried out in Aim 4 at Emory's Hope Clinic to assess safety, tolerability, immunogenicity and acceptability of influenza vaccination using a MN patch. Finally, Aim 5 will be based at PATH to assess regulatory, cost and policy issues associated with self-administered influenza vaccination. Expected outcomes from this research are (i) development of a low-cost MN patch that administers influenza vaccine in a simple, rapid manner, (ii) identification of immunologic differences and advantages of MN-based influenza vaccination compared to IM vaccination that will be used to improve the MN patch, (iii) production of MN patches for influenza vaccination under cGMP and IND approval from FDA, (iv) completion of a Phase I clinical trial assessing safety, tolerability, immunogenicity and acceptability of influenza vaccination using MN and (v) identification of regulatory, cost and policy issues to guide development and future introduction of our MN patch into clinical practice. These outcomes not only impact influenza vaccination, but also provide a basis for delivery of other vaccines and drugs using MN patches.

Public Health Relevance

Despite annual influenza vaccination campaigns, CDC attributes 36,000 deaths and 226,000 hospitalizations per year in the US to influenza, with an associated cost of ~$100 billion per year. As a quantum advance, this project will develop a novel microneedle patch designed to increase vaccination coverage by enabling simple, self-vaccination and increase vaccine immunogenicity by targeting antigen delivery to skin. The proposed Phase I clinical trial will provide the first human study of this technology.

National Institute of Health (NIH)
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Research Project--Cooperative Agreements (U01)
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Special Emphasis Panel (ZEB1-OSR-E (A1))
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Korte, Brenda
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Georgia Institute of Technology
Engineering (All Types)
Schools of Engineering
United States
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Pulit-Penaloza, Joanna A; Esser, E Stein; Vassilieva, Elena V et al. (2014) A protective role of murine langerin? cells in immune responses to cutaneous vaccination with microneedle patches. Sci Rep 4:6094
Gill, Harvinder S; Kang, Sang-Moo; Quan, Fu-Shi et al. (2014) Cutaneous immunization: an evolving paradigm in influenza vaccines. Expert Opin Drug Deliv 11:615-27
Norman, James J; Arya, Jaya M; McClain, Maxine A et al. (2014) Microneedle patches: usability and acceptability for self-vaccination against influenza. Vaccine 32:1856-62
Choi, Hyo-Jick; Bondy, Brian J; Yoo, Dae-Goon et al. (2013) Stability of whole inactivated influenza virus vaccine during coating onto metal microneedles. J Control Release 166:159-71
Koutsonanos, Dimitrios G; Compans, Richard W; Skountzou, Ioanna (2013) Targeting the skin for microneedle delivery of influenza vaccine. Adv Exp Med Biol 785:121-32
Andrews, Samantha N; Jeong, Eunhye; Prausnitz, Mark R (2013) Transdermal delivery of molecules is limited by full epidermis, not just stratum corneum. Pharm Res 30:1099-109
del Pilar Martin, Maria; Weldon, William C; Zarnitsyn, Vladimir G et al. (2012) Local response to microneedle-based influenza immunization in the skin. MBio 3:e00012-12
Kim, Yeu-Chun; Song, Jae-Min; Lipatov, Aleksandr S et al. (2012) Increased immunogenicity of avian influenza DNA vaccine delivered to the skin using a microneedle patch. Eur J Pharm Biopharm 81:239-47
Kim, Y C; Jarrahian, C; Zehrung, D et al. (2012) Delivery systems for intradermal vaccination. Curr Top Microbiol Immunol 351:77-112
Gupta, Jyoti; Park, Sohyun S; Bondy, Brian et al. (2011) Infusion pressure and pain during microneedle injection into skin of human subjects. Biomaterials 32:6823-31

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