Liposomal adjuvants for human vaccines

被引:96
作者
Alving, Carl R. [1 ]
Beck, Zoltan [1 ,2 ]
Matyas, Gary R. [1 ]
Rao, Mangala [1 ]
机构
[1] Walter Reed Army Inst Res, US Mil HIV Res Program, Lab Adjuvant & Antigen Res, 503 Robert Grant Ave, Silver Spring, MD 20910 USA
[2] Henry M Jackson Fdn Adv Mil Med, US Mil HIV Res Program, Bethesda, MD USA
关键词
Adjuvant; immunostimulation; liposomes; vaccine; MALARIA SPOROZOITE ANTIGEN; NONTOXIC LIPID-A; T-CELL RESPONSES; RECONSTITUTED INFLUENZA VIROSOMES; MEDIATED IMMUNE-RESPONSES; MYCOBACTERIUM-TUBERCULOSIS; DELIVERY-SYSTEMS; HEPATITIS-A; PHASE-I; IMMUNOLOGICAL ADJUVANTS;
D O I
10.1517/17425247.2016.1151871
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Liposomes are well-known as drug carriers, and are now critical components of two of six types of adjuvants present in licensed vaccines. The liposomal vaccine adjuvant field has long been dynamic and innovative, and research in this area is further examined as new commercial products appear in parallel with new vaccines. In an arena where successful products exist the potential for new types of vaccines with liposomal adjuvants, and alternative liposomal adjuvants that could emerge for new types of vaccines, are discussed. Areas covered: Major areas include: virosomes, constructed from phospholipids and proteins from influenza virus particles; liposomes containing natural and synthetic neutral or anionic phospholipids, cholesterol, natural or synthetic monophosphoryl lipid A, and QS21 saponin; non-phospholipid cationic liposomes; and combinations and mixtures of liposomes and immunostimulating ingredients as adjuvants for experimental vaccines. Expert opinion: Liposomes containing monophosphoryl lipid A and QS21 have considerable momentum that will result soon in emergence of prophylactic vaccines to malaria and shingles, and possible novel cancer vaccines. The licensed virosome vaccines to influenza and hepatitis A will be replaced with virosome vaccines to other infectious diseases. Alternative liposomal formulations are likely to emerge for difficult diseases such as tuberculosis or HIV-1 infection.
引用
收藏
页码:807 / 816
页数:10
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