Allison A C, Byars N E
J Immunol Methods. 1986 Dec 24;95(2):157-68. doi: 10.1016/0022-1759(86)90402-3.
Adjuvants are required to elicit protective immune responses with bacterial toxoids, inactivated viruses and subunit antigens produced by recombinant DNA technology. Some adjuvants, such as muramyl dipeptide (MDP) analog formulations, preferentially induce the formation of antibodies of isotypes that interact with complement and antibody-dependent effector cells, and do not elicit reaginic antibodies. Aluminum salts and mineral oil emulsions increase antibody formation but not cell-mediated immunity (CMI), whereas MDP formulations also elicit CMI. Adjuvants such as MDP and lipopolysaccharide (LPS) stimulate the production by accessory cells of IL-1 that increases the circulation of lymphocytes through draining lymph nodes and act as a growth factor for lymphocytes. Vehicles such as mineral oil emulsions, liposomes and Pluronic polymer formulations provide large surface areas on which antigens can be retained in a two-dimensional matrix, from which they can readily be transferred to antigen-presenting cells. The development of an adjuvant formulation able to elicit the formation of protective antibodies and CMI without unacceptable side effects is described.
佐剂是诱导针对细菌类毒素、灭活病毒和重组DNA技术生产的亚单位抗原产生保护性免疫反应所必需的。一些佐剂,如胞壁酰二肽(MDP)类似物制剂,优先诱导与补体和抗体依赖性效应细胞相互作用的同种型抗体的形成,且不引发反应素抗体。铝盐和矿物油乳剂可增加抗体形成,但不增强细胞介导免疫(CMI),而MDP制剂也可引发CMI。诸如MDP和脂多糖(LPS)等佐剂刺激辅助细胞产生IL-1,IL-1可增加淋巴细胞通过引流淋巴结的循环,并作为淋巴细胞的生长因子。诸如矿物油乳剂、脂质体和普朗尼克聚合物制剂等载体提供了大的表面积,抗原可保留在二维基质上,从该基质中它们可轻易转移至抗原呈递细胞。本文描述了一种能够诱导保护性抗体形成和CMI且无不可接受副作用的佐剂制剂的研发情况。