诱导CD8+细胞毒性T淋巴细胞对可溶性抗原的反应,同时给予一种新的muramyl二肽佐剂,n -乙酰- d -葡萄糖氨基-(β 1-4)- n -乙酰muramyl- l- alanyl- d -异谷氨酰胺(GMDP)

Therapeutic immunology Pub Date : 1995-02-01
R L Hornung, D L Longo, V L Gowda, L W Kwak
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引用次数: 0

摘要

我们已经研究了新的muramyl二肽GMDP作为诱导卵清蛋白(OVA)特异性CD8+细胞毒性T淋巴细胞(CTL)反应的佐剂的能力。C57Bl/6小鼠用含有(STP-GMDP)或不含(STP) GMDP的Tween-80载体L121 pluronic经角鲨烷乳化的50微克卵细胞两次免疫s.c.。用STP- gmdp免疫的小鼠体外再刺激5天后,检测到脾脏前体CD8+ CTL对E.G7-OVA的活性,但对EL-4亲代靶标没有活性,而单独用STP免疫的小鼠或单独用OVA免疫的小鼠均未显示CTL活性。在不含GMDP的微流态化STP载体制剂中乳化的OVA也能诱导出E.G7-OVA前体CTL。GMDP诱导对可溶性蛋白抗原产生i类限制性CD8+ CTL反应的能力,可能对开发有用的针对病毒性病原体或需要CTL反应的肿瘤的疫苗具有指导意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Induction of a CD8+ cytotoxic T lymphocyte response to soluble antigen given together with a novel muramyl dipeptide adjuvant, N-acetyl-D-glucosaminyl-(beta 1-4)-N-acetylmuramyl-L-alanyl-D-isoglutamine (GMDP).

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.

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