WorldWide Medicinal Chemistry, Pfizer, 610 Main Street, Cambridge, Massachusetts 02139, USA.
Nat Chem. 2015 Dec;7(12):952-60. doi: 10.1038/nchem.2396.
Vaccines have typically been prepared using whole organisms. These are normally either attenuated bacteria or viruses that are live but have been altered to reduce their virulence, or pathogens that have been inactivated and effectively killed through exposure to heat or formaldehyde. However, using whole organisms to elicit an immune response introduces the potential for infections arising from a reversion to a virulent form in live pathogens, unproductive reactions to vaccine components or batch-to-batch variability. Synthetic vaccines, in which a molecular antigen is conjugated to a carrier protein, offer the opportunity to circumvent these problems. This Perspective will highlight the progress that has been achieved in developing synthetic vaccines using a variety of molecular antigens. In particular, the different approaches used to develop conjugate vaccines using peptide/proteins, carbohydrates and other small molecule haptens as antigens are compared.
疫苗通常使用整个生物体来制备。这些生物体通常是减毒的细菌或病毒,它们仍然是活的,但已经被改变以降低其毒性,或者是已经失活并通过暴露于热或甲醛有效杀死的病原体。然而,使用整个生物体来引发免疫反应会带来从活病原体中恢复到毒性形式的感染的潜在风险,对疫苗成分的无效反应或批次间的可变性。将分子抗原与载体蛋白缀合的合成疫苗提供了规避这些问题的机会。本观点将重点介绍使用各种分子抗原开发合成疫苗所取得的进展。特别是,比较了使用肽/蛋白质、碳水化合物和其他小分子半抗原作为抗原开发结合疫苗所采用的不同方法。