Infectious Disease Research Institute, 1616 Eastlake Ave E, Suite 400, Seattle, WA 98102 USA.
Semin Immunol. 2018 Oct;39:22-29. doi: 10.1016/j.smim.2018.10.004. Epub 2018 Oct 23.
Lipopolysaccharide (LPS) is a well-defined agonist of Toll-like receptor (TLR) 4 that activates innate immune responses and influences the development of the adaptive response during infection with Gram-negative bacteria. Many years ago, Dr. Edgar Ribi separated the adjuvant activity of LPS from its toxic effects, an effort that led to the development of monophosphoryl lipid A (MPL). MPL, derived from Salmonella minnesota R595, has progressed through clinical development and is now used in various product-enabling formulations to support the generation of antigen-specific responses in several commercial and preclinical vaccines. We have generated several synthetic lipid A molecules, foremost glucopyranosyl lipid adjuvant (GLA) and second-generation lipid adjuvant (SLA), and have advanced these to clinical trial for various indications. In this review we summarize the potential and current positioning of TLR4-based adjuvant formulations in approved and emerging vaccines.
脂多糖(LPS)是 Toll 样受体 4(TLR4)的一种明确的激动剂,可激活先天免疫反应,并影响革兰氏阴性菌感染期间适应性反应的发展。许多年前,Edgar Ribi 博士将 LPS 的佐剂活性与其毒性作用分离,这一努力导致了单磷酰脂质 A(MPL)的发展。MPL 源自 Salmonella minnesota R595,已通过临床开发,并在各种产品使能配方中使用,以支持几种商业和临床前疫苗中抗原特异性反应的产生。我们已经生成了几种合成脂质 A 分子,主要是葡糖基脂质佐剂(GLA)和第二代脂质佐剂(SLA),并已将这些推进到各种适应症的临床试验中。在这篇综述中,我们总结了基于 TLR4 的佐剂配方在已批准和新兴疫苗中的潜力和当前定位。