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Liposomes Used As a Vaccine Adjuvant-delivery System: From Basics to Clinical Immunization

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Specialty Pharmacology
Date 2019 Apr 26
PMID 31022431
Citations 96
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Abstract

Liposomes are widely utilized as a carrier to improve therapeutic efficacy of agents thanks to their merits of high loading capacity, targeting delivery, reliable protection of agents, good biocompatibility, versatile structure modification and adjustable characteristics, such as size, surface charge, membrane flexibility and the agent loading mode. In particular, in recent years, through modification with immunopotentiators and targeting molecules, and in combination with innovative immunization devices, liposomes are rapidly developed as a multifunctional vaccine adjuvant-delivery system (VADS) that has a high capability in inducing desired immunoresponses, as they can target immune cells and even cellular organelles, engender lysosome escape, and promote Ag cross-presentation, thus enormously enhancing vaccination efficacy. Moreover, after decades of development, several products developed on liposome VADS have already been authorized for clinical immunization and are showing great advantages over conventional vaccines. This article describes in depth some critical issues relevant to the development of liposomes as a VADS, including principles underlying immunization, physicochemical properties of liposomes as the immunity-influencing factors, functional material modification to enhance immunostimulatory functions, the state-of-the-art liposome VADSs, as well as the marketed vaccines based on a liposome VADS. Therefore, this article provides a comprehensive reference to the development of novel liposome vaccines.

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References
1.
Cunningham A, Lal H, Kovac M, Chlibek R, Hwang S, Diez-Domingo J . Efficacy of the Herpes Zoster Subunit Vaccine in Adults 70 Years of Age or Older. N Engl J Med. 2016; 375(11):1019-32. DOI: 10.1056/NEJMoa1603800. View

2.
van Houte A, Snippe H, Schmitz M, Willers J . Characterization of immunogenic properties of haptenated liposomal model membranes in mice. V. Effect of membrane composition on humoral and cellular immunogenicity. Immunology. 1981; 44(3):561-8. PMC: 1554971. View

3.
Schneider J, Balu-Iyer S . Phosphatidylserine Converts Immunogenic Recombinant Human Acid Alpha-Glucosidase to a Tolerogenic Form in a Mouse Model of Pompe Disease. J Pharm Sci. 2016; 105(10):3097-3104. PMC: 5021602. DOI: 10.1016/j.xphs.2016.06.018. View

4.
Lasic D . Novel applications of liposomes. Trends Biotechnol. 1998; 16(7):307-21. DOI: 10.1016/s0167-7799(98)01220-7. View

5.
Dendouga N, Fochesato M, Lockman L, Mossman S, Giannini S . Cell-mediated immune responses to a varicella-zoster virus glycoprotein E vaccine using both a TLR agonist and QS21 in mice. Vaccine. 2012; 30(20):3126-35. DOI: 10.1016/j.vaccine.2012.01.088. View