Tagliabue A, Boraschi D
Biotechnology Department, Dompe SpA, L'Aquila, Italy.
Vaccine. 1993;11(5):594-5. doi: 10.1016/0264-410x(93)90240-x.
The possibility of preventing infectious diseases by employing efficacious vaccine is rapidly growing as a consequence of the new technologies in recombinant DNA and protein chemistry. However, the increasing number of synthetic and recombinant antigens further stresses the role of appropriate adjuvants to ensure maximal vaccine activity and the protection of all vaccinees. Several approaches can be applied to develop safe and effective agents capable of enhancing specific immune responses which can then protect the host from the pathogen. Among others, the direct use as adjuvant of those cytokines which are induced in animals by the classical Freund's adjuvants has recently become a matter of investigation. In particular, interleukin 1 (IL-1) has been shown to possess adjuvant activity for a variety of infectious and tumour antigens. However, the numerous side effects associated with the proinflammatory action of IL-1 represent a serious disadvantage for its use as a vaccine adjuvant. It was therefore of great interest that a nonpeptide contained in the IL-1 beta sequence (residues 163-171 corresponding to the sequence VQGEESNDK) is devoid of all proinflammatory activities but maintains the immunostimulating activity of the whole IL-1 beta. Thus, peptide 163-171 was successfully employed in animals to potentiate the specific immune response against T-helper-dependent cellular antigens, T helper-independent polysaccharidic antigens and recombinant as well as synthetic antigenic preparations derived from human pathogens. Furthermore, IL-1 and peptide 163-171 have been successfully used in tumour vaccines in experimental systems. It can therefore be concluded that peptide 163-171 is potentially a good candidate as vaccine adjuvant for human use.
由于重组DNA和蛋白质化学领域的新技术,通过使用有效的疫苗来预防传染病的可能性正在迅速增加。然而,合成和重组抗原数量的不断增加进一步凸显了合适佐剂的作用,以确保最大的疫苗活性并保护所有接种者。可以采用几种方法来开发能够增强特异性免疫反应的安全有效制剂,从而保护宿主免受病原体侵害。其中,直接将经典弗氏佐剂在动物体内诱导产生的细胞因子用作佐剂最近已成为研究的课题。特别是,白细胞介素1(IL-1)已被证明对多种感染性和肿瘤抗原具有佐剂活性。然而,与IL-1的促炎作用相关的众多副作用是其用作疫苗佐剂的严重缺点。因此,令人非常感兴趣的是,IL-1β序列中包含的一种非肽(对应于序列VQGEESNDK的163-171位残基)没有所有促炎活性,但保留了整个IL-1β的免疫刺激活性。因此,肽163-171已成功用于动物,以增强针对T辅助细胞依赖性细胞抗原、T辅助细胞非依赖性多糖抗原以及源自人类病原体的重组和合成抗原制剂的特异性免疫反应。此外,IL-1和肽163-171已在实验系统中的肿瘤疫苗中成功使用。因此可以得出结论,肽163-171可能是一种很好的人类疫苗佐剂候选物。