Staruch M J, Wood D D
J Immunol. 1982 Jan;128(1):155-60.
The possibility that the adjuvanticity of N-acetylmuramyl-L-alanyl-D-isoglutamine (MDP) is under genetic control in mice was examined. It was observed that MDP markedly enhances the secondary antibody response of BALB/c mice to bovine albumin but has little enhancing effect on C57BL/10Sn (B10) mice under the same conditions. This strain difference was not abolished by variations in the amount of MDP, the immunization protocol, the assay method, or the antigen used. An analysis of inbred and congenic strains showed that the responsiveness to MDP was influenced by at least two genes, one inside and one outside of the major histocompatibility complex. Mice with the C57BL background and/or the H-2b genome responded weakly to the adjuvant action of MDP, whereas those with the BALB/c or C3H background and/or H-2d or H-2k haplotypes responded more strongly. It is anticipated that the analysis of the mechanism of adjuvanticity of MDP will be facilitated by the use of mice that differ in their response to the adjuvant action of MDP.
研究了N-乙酰胞壁酰-L-丙氨酰-D-异谷氨酰胺(MDP)的佐剂活性在小鼠中受遗传控制的可能性。观察到,在相同条件下,MDP可显著增强BALB/c小鼠对牛血清白蛋白的二次抗体反应,但对C57BL/10Sn(B10)小鼠的增强作用很小。这种品系差异不会因MDP的用量、免疫方案、检测方法或所用抗原的变化而消除。对近交系和同源近交系的分析表明,对MDP的反应性至少受两个基因影响,一个在主要组织相容性复合体内,一个在其外。具有C57BL背景和/或H-2b基因组的小鼠对MDP的佐剂作用反应较弱,而具有BALB/c或C3H背景和/或H-2d或H-2k单倍型的小鼠反应更强。预计,利用对MDP佐剂作用反应不同的小鼠,将有助于对MDP佐剂活性机制的分析。