Weeratna R D, McCluskie M J, Xu Y, Davis H L
Loeb Health Research Institute at the Ottawa Hospital, 725 Parkdale Avenue, Ottawa, Canada.
Vaccine. 2000 Mar 6;18(17):1755-62. doi: 10.1016/s0264-410x(99)00526-5.
The ability to augment protective immune responses with minimal side effects is quintessential for a good adjuvant. This study has compared various adjuvants that are used in animal research (Freund's complete and incomplete adjuvants, Titermax Gold), are licensed for human use (alum), or are in clinical testing for humans (monophosphoryl lipid, CpG DNA), for their ability to augment humoral responses to a model antigen (hepatitis B surface antigen) and for the degree of damage they caused in the injected muscle. According to the data, the adjuvant combination CpG DNA+alum had the greatest potential to augment immune responses with minimal side effects at the injection site. Evaluation of antibody isotypes indicated Th2 responses (no IgG2a) with all adjuvants except monophosphoryl lipid and CpG DNA, which gave mixed Th1/Th2 responses (IgG1 and IgG2a). Strong Th1 responses (predominantly IgG2a) were obtained with combinations of CpG DNA with other adjuvants.
以最小的副作用增强保护性免疫反应的能力是优良佐剂的关键特性。本研究比较了多种用于动物研究的佐剂(弗氏完全佐剂和不完全佐剂、Titermax Gold)、已获人类使用许可的佐剂(明矾)或正在进行人体临床试验的佐剂(单磷酰脂质、CpG DNA),比较它们增强对模型抗原(乙肝表面抗原)的体液反应的能力以及它们在注射肌肉中造成的损伤程度。根据数据,佐剂组合CpG DNA + 明矾在注射部位以最小副作用增强免疫反应的潜力最大。抗体亚型评估表明,除单磷酰脂质和CpG DNA产生混合的Th1/Th2反应(IgG1和IgG2a)外,所有佐剂均产生Th2反应(无IgG2a)。CpG DNA与其他佐剂组合可产生强烈的Th1反应(主要为IgG2a)。