Gupta R K, Siber G R
Massachusetts Public Health Biologic Laboratories, State Laboratory Institute, Boston 02130, USA.
Vaccine. 1995 Oct;13(14):1263-76. doi: 10.1016/0264-410x(95)00011-o.
Adjuvants help antigen to elicit an early, high and long-lasting immune response with less antigen, thus saving on vaccine production costs. In recent years, adjuvants received much attention because of the development of purified, subunit and synthetic vaccines which are poor immunogens and require adjuvants to evoke the immune response. With the use of adjuvants immune response can be selectively modulated to major histocompatibility complex (MHC) class I or MHC class II and Th1 or Th2 type, which is very important for protection against diseases caused by intracellular pathogens such as viruses, parasites and bacteria (Mycobacterium). A number of problems are encountered in the development and use of adjuvants for human vaccines. The biggest issue with the use of adjuvants for human vaccines, particularly routine childhood vaccines, is the toxicity and adverse side-effects of most of the adjuvant formulations. At present the choice of adjuvants for human vaccination reflects a compromise between a requirement for adjuvanticity and an acceptable low level of side-effects. Other problems with the development of adjuvants include restricted adjuvanticity of certain formulations to a few antigens, use of aluminum adjuvants as reference adjuvant preparations under suboptimal conditions, non-availability of reliable animal models, use of non-standard assays and biological differences between animal models and humans leading to the failure of promising formulations to show adjuvanticity in clinical trials. The most common adjuvants for human use today are still aluminum hydroxide and aluminum phosphate, although calcium phosphate and oil emulsions also have some use in human vaccinations. During the last 15 years much progress has been made on development, isolation and chemical synthesis of alternative adjuvants such as derivatives of muramyl dipeptide, monophosphoryl lipid A, liposomes, QS21, MF-59 and immunostimulating complexes (ISCOMS). Other areas in adjuvant research which have received much attention are the controlled release of vaccine antigens using biodegradable polymer microspheres and reciprocal enhanced immunogenicity of protein-polysaccharide conjugates. Biodegradable polymer microspheres are being evaluated for targeting antigens on mucosal surfaces and for controlled release of vaccines with an aim to reduce the number of doses required for primary immunization. Reciprocal enhanced immunogenicity of protein-polysaccharide conjugates will be useful for the development of combination vaccines.
佐剂有助于抗原以较少的抗原引发早期、强烈且持久的免疫反应,从而节省疫苗生产成本。近年来,由于纯化疫苗、亚单位疫苗和合成疫苗的发展,佐剂受到了广泛关注,这些疫苗免疫原性较差,需要佐剂来引发免疫反应。通过使用佐剂,免疫反应可以被选择性地调节为主要组织相容性复合体(MHC)I类或MHC II类以及Th1或Th2型,这对于预防由细胞内病原体如病毒、寄生虫和细菌(分枝杆菌)引起的疾病非常重要。在人类疫苗佐剂的开发和使用中遇到了一些问题。在人类疫苗中使用佐剂,尤其是常规儿童疫苗,最大的问题是大多数佐剂配方的毒性和不良副作用。目前,用于人类疫苗接种的佐剂选择反映了在佐剂活性需求和可接受的低副作用水平之间的权衡。佐剂开发的其他问题包括某些配方对少数抗原的佐剂活性受限、在次优条件下将铝佐剂用作参考佐剂制剂、缺乏可靠的动物模型、使用非标准检测方法以及动物模型与人类之间的生物学差异导致有前景的配方在临床试验中未能显示出佐剂活性。目前人类最常用的佐剂仍然是氢氧化铝和磷酸铝,尽管磷酸钙和油乳剂在人类疫苗接种中也有一些应用。在过去的15年里,在替代佐剂的开发、分离和化学合成方面取得了很大进展,如胞壁酰二肽衍生物、单磷酰脂质A衍生物、脂质体、QS21、MF - 59和免疫刺激复合物(ISCOMS)。佐剂研究中受到广泛关注的其他领域包括使用可生物降解聚合物微球控制疫苗抗原的释放以及蛋白质 - 多糖偶联物的相互增强免疫原性。可生物降解聚合物微球正在被评估用于靶向粘膜表面的抗原以及控制疫苗的释放,目的是减少初次免疫所需的剂量数。蛋白质 - 多糖偶联物的相互增强免疫原性将有助于联合疫苗的开发。