Suppr超能文献

通过短合成肽和白细胞介素-7体外刺激诱导原发性抗病毒细胞毒性T细胞

Induction of primary anti-viral cytotoxic T cells by in vitro stimulation with short synthetic peptide and interleukin-7.

作者信息

Kos F J, Müllbacher A

机构信息

Division of Cell Biology, John Curtin School of Medical Research, Australian National University, Canberra.

出版信息

Eur J Immunol. 1992 Dec;22(12):3183-5. doi: 10.1002/eji.1830221224.

Abstract

The present study investigated whether a short synthetic peptide NPP, with a modified sequence (147-158 R156-) derived from influenza A virus nucleoprotein with high affinity for Kd major histocompatibility complex class I molecules, could induce primary influenza virus-specific cytotoxic T (Tc) cells in vitro. Naive BALB/c (H-2d) splenocytes did not respond to the stimulation with only NPP with the generation of effector Tc cells specific for influenza A virus-infected target cells in vitro. However, they were able to do so if cultured with NPP in the presence of IL-7. IL-7 activity in this system differed significantly from IL-2 activity in the specificity of the effect. The use of exogenous IL-2, instead of IL-7, with NPP resulted in the induction of lytic cells that lysed both influenza virus-infected and uninfected syngeneic target cells. These results suggest that IL-7 is a potent regulatory cytokine in the antigen-specific activation of resting naive Tc cell precursors and may provide the necessary conditions for the induction of human primary Tc cells in vitro.

摘要

本研究调查了一种短合成肽NPP,其具有源自甲型流感病毒核蛋白的修饰序列(147 - 158 R156 -),对Kd主要组织相容性复合体I类分子具有高亲和力,是否能在体外诱导出原发性流感病毒特异性细胞毒性T(Tc)细胞。未致敏的BALB/c(H - 2d)脾细胞仅用NPP刺激时,在体外不会产生针对甲型流感病毒感染靶细胞的效应Tc细胞。然而,如果在IL - 7存在的情况下与NPP一起培养,它们就能产生效应Tc细胞。该系统中IL - 7的活性在效应特异性方面与IL - 2的活性有显著差异。用外源性IL - 2而非IL - 7与NPP一起使用,会诱导出既能裂解甲型流感病毒感染的同基因靶细胞,又能裂解未感染的同基因靶细胞的溶细胞。这些结果表明,IL - 7是静息未致敏Tc细胞前体抗原特异性激活中的一种有效调节细胞因子,可能为体外诱导人原发性Tc细胞提供必要条件。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验