Lowy I, Theze J, Chedid L
J Immunol. 1980 Jan;124(1):100-4.
Specific anti-dinitrophenyl (DNP) response to DNP-conjugated L-glutamine60-L-alanine30-L-tyrosine10 (DNP-GAT) was obtained in GAT-responder mice by using synthetic N-acetylmuramyl-L-alanyl-D-isoglutamine (MDP) as adjuvant. Significant levels of anti-DNP antibodies were observed during a secondary response to DNP-GAT, when both antigen and MDP were used for priming. In this system, MDP was able to prime the carrier-specific T cells but not the hapten specific B cells. The study of the isotypic pattern of the anti-DNP response shows that MDP stimulates only the appearance of specific anti-DNP IgG1 plaque-forming cells. Anti-DNP plaque-forming cells were stimulated in animals primed with DNP-GAT in Freund's complete adjuvant or in Maalox-pertussis and used as control IgG1, IgG2a, and IgG2b.
通过使用合成的N-乙酰胞壁酰-L-丙氨酰-D-异谷氨酰胺(MDP)作为佐剂,在对GAT有反应的小鼠中获得了对二硝基苯基(DNP)偶联的L-谷氨酰胺60-L-丙氨酸30-L-酪氨酸10(DNP-GAT)的特异性抗DNP反应。当抗原和MDP都用于初次免疫时,在对DNP-GAT的二次反应期间观察到了显著水平的抗DNP抗体。在这个系统中,MDP能够启动载体特异性T细胞,但不能启动半抗原特异性B细胞。对抗DNP反应的同种型模式的研究表明,MDP仅刺激特异性抗DNP IgG1斑块形成细胞的出现。在用弗氏完全佐剂或氢氧化铝-百日咳中用DNP-GAT进行初次免疫的动物中刺激抗DNP斑块形成细胞,并用作对照IgG1、IgG2a和IgG2b。