Edelman R
Rev Infect Dis. 1980 May-Jun;2(3):370-83. doi: 10.1093/clinids/2.3.370.
Nonreplicating, purified subunit or synthetic viral vaccines of the future are likely to be weak immunogens that will require immunopotentiation if they are to be effective. These marginal vaccines could be improved by combination with potent and safe immunologic adjuvants. The use of adjuvants should also reduce the amount of purified antigen required for successful immunization, thus making vaccine production more economical and more feasible. It may be possible to combine the recently developed relatively nontoxic synthetic immunoregulators of low molecular weight with antigens in order to modulate preselected compartments of the immune system. To date, the question of adjuvant safety has not been resolved and represents the major obstacle to the orderly development of adjuvanted vaccines. The fear of inducing cancer and other immediate or long-term perturbations of the immune system must be patently and rationally overcome by basic and applied experimentation and by the development of appropriate guidelines for studies in humans.
未来的非复制型、纯化亚单位或合成病毒疫苗很可能是弱免疫原,如果要使其有效,将需要进行免疫增强。这些效果欠佳的疫苗可以通过与高效且安全的免疫佐剂联合使用来加以改进。使用佐剂还应能减少成功免疫所需的纯化抗原量,从而使疫苗生产更经济且更可行。有可能将最近开发的相对无毒的低分子量合成免疫调节剂与抗原结合,以调节免疫系统的预选区室。迄今为止,佐剂安全性问题尚未得到解决,这是佐剂疫苗有序开发的主要障碍。必须通过基础和应用实验以及制定适当的人体研究指南,切实且合理地克服对诱发癌症和免疫系统其他即时或长期干扰的担忧。