Zariri Afshin, van der Ley Peter
Institute for Translational Vaccinology (InTraVacc), Antonie van Leeuwenhoeklaan 9, 3721 MA Bilthoven, The Netherlands.
Expert Rev Vaccines. 2015 Jun;14(6):861-76. doi: 10.1586/14760584.2015.1026808. Epub 2015 Mar 22.
Lipopolysaccharide (LPS), a dominant component of the Gram-negative bacterial outer membrane, is a strong activator of the innate immune system, and thereby an important determinant in the adaptive immune response following bacterial infection. This adjuvant activity can be harnessed following immunization with bacteria-derived vaccines that naturally contain LPS, and when LPS or molecules derived from it are added to purified vaccine antigens. However, the downside of the strong biological activity of LPS is its ability to contribute to vaccine reactogenicity. Modification of the LPS structure allows triggering of a proper immune response needed in a vaccine against a particular pathogen while at the same time lowering its toxicity. Extensive modifications to the basic structure are possible by using our current knowledge of bacterial genes involved in LPS biosynthesis and modification. This review focuses on biosynthetic engineering of the structure of LPS and implications of these modifications for generation of safe adjuvants.
脂多糖(LPS)是革兰氏阴性菌外膜的主要成分,是先天免疫系统的强激活剂,因此也是细菌感染后适应性免疫反应的重要决定因素。在用天然含有LPS的细菌衍生疫苗免疫后,以及当LPS或其衍生分子添加到纯化的疫苗抗原中时,这种佐剂活性可以被利用。然而,LPS强大生物活性的缺点是它会导致疫苗反应原性。LPS结构的修饰能够引发针对特定病原体的疫苗所需的适当免疫反应,同时降低其毒性。利用我们目前对参与LPS生物合成和修饰的细菌基因的了解,可以对其基本结构进行广泛修饰。本综述重点关注LPS结构的生物合成工程以及这些修饰对安全佐剂产生的影响。