| Literature DB >> 22406456 |
Celine A Hayden1, Stephen J Streatfield, Barry J Lamphear, Gina M Fake, Todd K Keener, John H Walker, John D Clements, Debra D Turner, Ian R Tizard, John A Howard.
Abstract
Hepatitis B remains a major global health problem despite the availability of a safe and effective vaccine. Segments of the population lack access to or respond poorly to the parenteral vaccine, perpetuating the infection-transmission cycle. A low cost, orally delivered vaccine has the potential to alleviate many of these problems. Here we describe the expression of a bioencapsulated hepatitis B surface antigen (HBsAg) in maize and its immunogenicity, demonstrating for the first time a commercially feasible oral subunit vaccine production system for a major disease. This work surmounts previous barriers to plant-produced vaccines by expressing HBsAg at much higher levels and retaining antigen immunogenicity post-processing: factors which facilitated a robust immune response in mice without the need for an adjuvant. This method provides a practical solution to the delivery of a low-cost, stable oral vaccine.Entities:
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Year: 2012 PMID: 22406456 PMCID: PMC3322283 DOI: 10.1016/j.vaccine.2012.02.072
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641