TY - JOUR
T1 - Production of virus-like particles for vaccines
AU - Fuenmayor, J.
AU - Gòdia, F.
AU - Cervera, L.
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017/10/25
Y1 - 2017/10/25
N2 - Virus-like particles (VLPs) are nanostructures that resemble the structures of viruses. They are composed of one or more structural proteins that can be arranged in several layers and can also contain a lipid outer envelope. VLPs trigger a high humoral and cellular immune response due to their repetitive structures. A key factor regarding VLP safety is the lack of viral genomic material, which enhances safety during both manufacture and administration. Contemporary VLP production may take advantage of several systems, including bacterial, yeast, insect and mammalian cells. The choice of production platform depends on several factors, including cost and the need for post-translational modifications (PTMs), which can be essential in generating an optimal immune response. Some VLP-based vaccines designed to prevent several infectious diseases are already approved and on the market, with many others at the clinical trial or research stage. Interest in this technology has recently increased due to its advantages over classical vaccines. This paper reviews the state-of-the-art of VLP production systems and the newest generation of VLP-based vaccines now available.
AB - Virus-like particles (VLPs) are nanostructures that resemble the structures of viruses. They are composed of one or more structural proteins that can be arranged in several layers and can also contain a lipid outer envelope. VLPs trigger a high humoral and cellular immune response due to their repetitive structures. A key factor regarding VLP safety is the lack of viral genomic material, which enhances safety during both manufacture and administration. Contemporary VLP production may take advantage of several systems, including bacterial, yeast, insect and mammalian cells. The choice of production platform depends on several factors, including cost and the need for post-translational modifications (PTMs), which can be essential in generating an optimal immune response. Some VLP-based vaccines designed to prevent several infectious diseases are already approved and on the market, with many others at the clinical trial or research stage. Interest in this technology has recently increased due to its advantages over classical vaccines. This paper reviews the state-of-the-art of VLP production systems and the newest generation of VLP-based vaccines now available.
KW - culture mode
KW - immunogen
KW - production platform
KW - Recombinant vaccines
KW - virus-like particles
UR - http://www.scopus.com/inward/record.url?scp=85026795107&partnerID=8YFLogxK
U2 - 10.1016/j.nbt.2017.07.010
DO - 10.1016/j.nbt.2017.07.010
M3 - Article
C2 - 28778817
AN - SCOPUS:85026795107
SN - 1871-6784
VL - 39
SP - 174
EP - 180
JO - New Biotechnology
JF - New Biotechnology
ER -