Hornung R L, Longo D L, Gowda V L, Kwak L W
Biological Carcinogenesis & Development Program, Program Resources, Inc./DynCorp, Frederick, MD, USA.
Ther Immunol. 1995 Feb;2(1):7-14.
We have investigated the ability of the novel muramyl dipeptide, GMDP, to act as an adjuvant for the induction of ovalbumin (OVA)-specific, CD8+ cytotoxic T lymphocyte (CTL) responses. C57Bl/6 mice were twice immunized s.c. with 50 micrograms OVA emulsified with a squalane, L121 pluronic containing Tween-80 vehicle either with (STP-GMDP) or without (STP) GMDP. Splenic precursor CD8+ CTL activity against E.G7-OVA, but not against EL-4 parental targets was detected in STP-GMDP immunized mice after 5 days of in vitro re-stimulation with irradiated E.G7-OVA cells, while mice immunized with OVA in STP alone or OVA alone failed to demonstrate CTL activity. OVA emulsified in a microfluidized STP vehicle formulation without GMDP also elicited the E.G7-OVA precursor CTL. The ability of GMDP to induce a class I-restricted, CD8+ CTL response to a soluble protein antigen may have implications for the development of useful vaccines against viral pathogens or tumours against which CTL responses are desirable.
我们研究了新型胞壁酰二肽GMDP作为佐剂诱导卵清蛋白(OVA)特异性CD8⁺细胞毒性T淋巴细胞(CTL)反应的能力。C57Bl/6小鼠分两次皮下免疫,用50微克OVA与角鲨烷、含吐温80的L121普朗尼克乳化剂混合,其中一组添加GMDP(STP-GMDP),另一组不添加GMDP(STP)。在体外经辐照的E.G7-OVA细胞再刺激5天后,在STP-GMDP免疫的小鼠中检测到针对E.G7-OVA而非EL-4亲本靶标的脾前体CD8⁺CTL活性,而单独用STP中的OVA免疫或仅用OVA免疫的小鼠未表现出CTL活性。在无微流化GMDP的STP载体配方中乳化的OVA也引发了E.G7-OVA前体CTL。GMDP诱导对可溶性蛋白抗原的I类限制性CD8⁺CTL反应的能力可能对开发针对病毒病原体或肿瘤的有用疫苗具有意义,对于这些病原体或肿瘤,CTL反应是可取的。