| Literature DB >> 28965203 |
Dania O Govea-Alonso1,2, Marlene A Tello-Olea1,2, Josué Beltrán-López1,2, Elizabeth Monreal-Escalante1,2, Jorge A Salazar-Gonzalez1,2, Bernardo Bañuelos-Hernández1,2, Sergio Rosales-Mendoza3,4.
Abstract
Atherosclerosis is a pathology leading to cardiovascular diseases with high epidemiologic impact; thus, new therapies are required to fight this global health issue. Immunotherapy is a feasible approach to treat atherosclerosis and given that genetically engineered plants are attractive hosts for vaccine development; we previously proved that the plant cell is able to synthesize a chimeric protein called CTB:p210:CETPe, which is composed of the cholera toxin B subunit (CTB) as immunogenic carrier and target epitopes from the cholesteryl ester transfer protein (CETP461-476) and apolipoprotein B100 (p210). Since CTB:p210:CETPe was expressed in tobacco at sufficient levels to evoke humoral responses in mice, its expression in carrot was explored in the present study looking to develop a vaccine in a safe host amenable for oral delivery; avoiding the purification requirement. Carrot cell lines expressing CTB:p210:CETPe were developed, showing accumulation levels up to 6.1 µg/g dry weight. An immunoblot analysis revealed that the carrot-made protein is antigenic and an oral mice immunization scheme led to evidence on the immunogenic activity of this protein; revealing its capability of inducing serum IgG responses against p210 and CETP epitopes. This study represents a step forward in the development of an attractive oral low-cost vaccine to treat atherosclerosis.Entities:
Keywords: Atherosclerosis; CETP; Carrot callus culture; Immunotherapy; Plant-based oral vaccine; p210
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Year: 2017 PMID: 28965203 DOI: 10.1007/s12033-017-0036-5
Source DB: PubMed Journal: Mol Biotechnol ISSN: 1073-6085 Impact factor: 2.695