Alter Galit, Sekaly Rafick Pierre
Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA, United States.
Case Western Reserve University, Cleveland, OH, United States.
Vaccine. 2015 Jun 8;33 Suppl 2:B55-9. doi: 10.1016/j.vaccine.2015.03.058.
Since the development of the first vaccine over 200 years ago, vaccines have saved millions of lives and have become the most cost-effective modern medical intervention. However, over 70 years ago, Freund recognized that the effectiveness of the vaccine-induced immune responses could be vastly improved via the co-delivery of inflammation-induced agents, giving birth to the adjuvant field. Since the first description of adjuvants, revolutionary discoveries, including the discovery of dendritic cells and pattern recognition receptors, that drive remarkably different biological profiles, have opened the landscape of opportunities for the development of novel adjuvants able to trigger a remarkably diverse inflammatory profiles, thereby qualitatively and quantitatively skewing adaptive immunity in a tailored manner against target pathogens. However, mounting data point to a critical role for pre-existing inflammation as a predictor of vaccine responsiveness. Thus, in this review we will discuss novel opportunities by which pre-existing inflammation may be modulated, skewed, or tuned via next-generation vaccine approaches to enhanced vaccine-induced immunity in the elderly, immunocompromised, or subjects with chronic diseases.
自200多年前第一种疫苗问世以来,疫苗已拯救了数百万人的生命,并成为最具成本效益的现代医学干预手段。然而,70多年前,弗罗因德认识到,通过共同递送炎症诱导剂,疫苗诱导的免疫反应的有效性可以得到极大提高,从而催生了佐剂领域。自从首次描述佐剂以来,包括树突状细胞和模式识别受体的发现在内的革命性发现,驱动了显著不同的生物学特征,为新型佐剂的开发开辟了机会,这些佐剂能够引发显著不同的炎症特征,从而以定制的方式定性和定量地改变适应性免疫以对抗目标病原体。然而,越来越多的数据表明,预先存在的炎症作为疫苗反应性的预测指标起着关键作用。因此,在本综述中,我们将讨论通过下一代疫苗方法调节、改变或调整预先存在的炎症的新机会,以增强老年人、免疫功能低下者或慢性病患者的疫苗诱导免疫。