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由包含人乳头瘤病毒16型E7蛋白的基于HIV-1的病毒样颗粒引发的抗肿瘤CD8 + T细胞免疫。

Anti-tumor CD8+ T cell immunity elicited by HIV-1-based virus-like particles incorporating HPV-16 E7 protein.

作者信息

Di Bonito Paola, Grasso Felicia, Mochi Stefania, Petrone Linda, Fanales-Belasio Emanuele, Mei Arianna, Cesolini Armando, Laconi Giuseppe, Conrad Heinke, Bernhard Helga, Dembek Claudia J, Cosma Antonio, Santini Stefano M, Lapenta Caterina, Donati Simona, Muratori Claudia, Giorgi Colomba, Federico Maurizio

机构信息

Department of Infectious, Parasitic and Immunomediated Diseases, Istituto Superiore di Sanità, Rome, Italy.

出版信息

Virology. 2009 Dec 5;395(1):45-55. doi: 10.1016/j.virol.2009.09.012. Epub 2009 Oct 2.

Abstract

Here we report a novel strategy for the induction of CD8(+) T cell adaptive immune response against viral and tumor antigens. This approach relies on high levels of incorporation in HIV-1 VLPs of a mutant of HIV-1 Nef (Nef(mut)) which can act as anchoring element for foreign proteins. By in vitro assay, we found that VLP-associated Nef(mut) is efficiently cross-presented by antigen presenting cells. Inoculation in mice of VLPs incorporating the HPV-16 E7 protein fused to Nef(mut) led to an anti-E7 CD8(+) T cell response much stronger than that elicited by E7 recombinant protein inoculated with incomplete Freund's adjuvant and correlating with well-detectable anti-E7 CTL activity. Most relevantly, mice immunized with Nef(mut)-E7 VLPs developed a protective immune response against tumors induced by E7 expressing tumor cells. These results make Nef(mut) VLPs a promising candidate for new vaccine strategies focused on the induction of CD8(+) T cell immunity.

摘要

在此,我们报告一种诱导针对病毒和肿瘤抗原的CD8(+) T细胞适应性免疫反应的新策略。该方法依赖于在HIV-1病毒样颗粒(VLPs)中高水平掺入HIV-1 Nef的一种突变体(Nef(mut)),它可作为外源蛋白的锚定元件。通过体外试验,我们发现与VLP相关的Nef(mut)能被抗原呈递细胞有效交叉呈递。给小鼠接种掺入与Nef(mut)融合的HPV-16 E7蛋白的VLPs,引发的抗E7 CD8(+) T细胞反应比用不完全弗氏佐剂接种E7重组蛋白所引发的反应强得多,且与可检测到的抗E7细胞毒性T淋巴细胞(CTL)活性相关。最相关的是,用Nef(mut)-E7 VLPs免疫的小鼠对由表达E7的肿瘤细胞诱导的肿瘤产生了保护性免疫反应。这些结果使Nef(mut) VLPs成为专注于诱导CD8(+) T细胞免疫的新疫苗策略的有希望的候选者。

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