Statens Serum Institut, Department of Infectious Disease Immunology, Copenhagen, Denmark.
Expert Rev Vaccines. 2011 Apr;10(4):513-21. doi: 10.1586/erv.11.17.
The application of cationic liposomes as vaccine delivery systems and adjuvants has been investigated extensively over the last few decades. However, cationic liposomes are, in general, not sufficiently immunostimulatory, which is why the combination of liposomes with immunostimulating ligands has arisen as a strategy in the development of novel adjuvant systems. Within the last 5 years, two novel adjuvant systems based on cationic liposomes incorporating Toll-like receptor or non-Toll-like receptor immunostimulating ligands have progressed from preclinical testing in smaller animal species to clinical testing in humans. The immune responses that these clinical candidates induce are primarily of the Th1 type for which there is a profound unmet need. Furthermore, a number of new cationic liposome-forming surfactants with notable immunostimulatory properties have been discovered. In this article we review the recent progress on the application of cationic liposomes as vaccine delivery systems/adjuvants.
在过去的几十年中,阳离子脂质体作为疫苗传递系统和佐剂的应用已经得到了广泛的研究。然而,阳离子脂质体通常没有足够的免疫刺激性,这就是为什么脂质体与免疫刺激配体的结合已经成为开发新型佐剂系统的一种策略。在过去的 5 年中,两种新型的基于阳离子脂质体的佐剂系统,其中包含 Toll 样受体或非 Toll 样受体免疫刺激配体,已经从小动物的临床前测试进展到了人体的临床测试。这些临床候选物诱导的免疫反应主要是 Th1 型,这方面存在着巨大的未满足的需求。此外,还发现了许多具有显著免疫刺激特性的新型阳离子脂质体形成表面活性剂。本文综述了阳离子脂质体作为疫苗传递系统/佐剂的最新研究进展。
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