Souders Nicholas C, Sewell Duane A, Pan Zhen-Kun, Hussain S Farzana, Rodriguez Alexander, Wallecha Anu, Paterson Yvonne
Department of Microbiology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Cancer Immun. 2007 Feb 6;7:2.
We have created a transgenic mouse with tissue-specific expression of the human papilloma virus (HPV) 16 E6 and E7 oncoproteins in the thyroid as a model of HPV transformed cancer. The expression of the transgenes results in the formation of palpable thyroid tumors. E7 is not expressed in other tissues but is expressed in medullary thymic epithelial cells, which have been implicated in the control of negative selection. We show that Listeria-based vaccines against E7 can induce the regression of solid implanted tumors in the transgenic mice, although at a lower frequency than in wild type (WT) mice. E7-specific CD8+ T cells induced in transgenic mice are of both lower avidity and lower frequency when compared to the WT mice. In this model, Listeria-based vaccines against E7 appear to be overcoming central tolerance by expanding low avidity CD8+ T cells specific for E7 that are not deleted during thymopoesis and can eliminate solid tumors.
我们构建了一种转基因小鼠,其甲状腺中特异性表达人乳头瘤病毒(HPV)16 E6和E7癌蛋白,作为HPV转化癌的模型。转基因的表达导致可触及的甲状腺肿瘤形成。E7不在其他组织中表达,但在髓质胸腺上皮细胞中表达,而髓质胸腺上皮细胞与阴性选择的控制有关。我们发现,基于李斯特菌的抗E7疫苗可诱导转基因小鼠体内实体植入肿瘤的消退,尽管其频率低于野生型(WT)小鼠。与WT小鼠相比,转基因小鼠中诱导产生的E7特异性CD8+ T细胞亲和力较低且频率较低。在该模型中,基于李斯特菌的抗E7疫苗似乎通过扩增对E7特异的低亲和力CD8+ T细胞来克服中枢耐受,这些细胞在胸腺生成过程中未被清除,并且能够消除实体肿瘤。