TY - JOUR
T1 - Mucoadhesive film for oral delivery of vaccines for protection of the respiratory tract
AU - Esih, Hana
AU - Mezgec, Klemen
AU - Billmeier, Martina
AU - Malenšek, Špela
AU - Benčina, Mojca
AU - Grilc, Blaž
AU - Vidmar, Sara
AU - Gašperlin, Mirjana
AU - Bele, Marjan
AU - Zidarn, Mihaela
AU - Zupanc, Tatjana Lejko
AU - Morgan, Tina
AU - Jordan, Ingo
AU - Sandig, Volker
AU - Schrödel, Silke
AU - Thirion, Christian
AU - Protzer, Ulrike
AU - Wagner, Ralf
AU - Lainšček, Duško
AU - Jerala, Roman
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/7
Y1 - 2024/7
N2 - The delivery of vaccines plays a pivotal role in influencing the strength and longevity of the immune response and controlling reactogenicity. Mucosal immunization, as compared to parenteral vaccination, could offer greater protection against respiratory infections while being less invasive. While oral vaccination has been presumed less effective and believed to target mainly the gastrointestinal tract, trans-buccal delivery using mucoadhesive films (MAF) may allow targeted delivery to the mucosa. Here we present an effective strategy for mucosal delivery of several vaccine platforms incorporated in MAF, including DNA plasmids, viral vectors, and lipid nanoparticles incorporating mRNA (mRNA/LNP). The mRNA/LNP vaccine formulation targeting SARS-CoV-2 as a proof of concept remained stable within MAF consisting of slowly releasing water-soluble polymers and an impermeable backing layer, facilitating enhanced penetration into the oral mucosa. This formulation elicited antibody and cellular responses comparable to the intramuscular injection, but also induced the production of mucosal IgAs, highlighting its efficacy, particularly for use as a booster vaccine and the potential advantage for protection against respiratory infections. The MAF vaccine preparation demonstrates significant advantages, such as efficient delivery, stability, and simple noninvasive administration with the potential to alleviate vaccine hesitancy.
AB - The delivery of vaccines plays a pivotal role in influencing the strength and longevity of the immune response and controlling reactogenicity. Mucosal immunization, as compared to parenteral vaccination, could offer greater protection against respiratory infections while being less invasive. While oral vaccination has been presumed less effective and believed to target mainly the gastrointestinal tract, trans-buccal delivery using mucoadhesive films (MAF) may allow targeted delivery to the mucosa. Here we present an effective strategy for mucosal delivery of several vaccine platforms incorporated in MAF, including DNA plasmids, viral vectors, and lipid nanoparticles incorporating mRNA (mRNA/LNP). The mRNA/LNP vaccine formulation targeting SARS-CoV-2 as a proof of concept remained stable within MAF consisting of slowly releasing water-soluble polymers and an impermeable backing layer, facilitating enhanced penetration into the oral mucosa. This formulation elicited antibody and cellular responses comparable to the intramuscular injection, but also induced the production of mucosal IgAs, highlighting its efficacy, particularly for use as a booster vaccine and the potential advantage for protection against respiratory infections. The MAF vaccine preparation demonstrates significant advantages, such as efficient delivery, stability, and simple noninvasive administration with the potential to alleviate vaccine hesitancy.
KW - Mucoadhesive film
KW - Mucosal immunity
KW - Respiratory infection
KW - Vaccine delivery
UR - http://www.scopus.com/inward/record.url?scp=85194301751&partnerID=8YFLogxK
U2 - 10.1016/j.jconrel.2024.05.041
DO - 10.1016/j.jconrel.2024.05.041
M3 - Article
AN - SCOPUS:85194301751
SN - 0168-3659
VL - 371
SP - 179
EP - 192
JO - Journal of Controlled Release
JF - Journal of Controlled Release
ER -