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接种含细胞毒性T淋巴细胞表位的肽可预防由16型人乳头瘤病毒转化细胞诱导的肿瘤。

Vaccination with cytotoxic T lymphocyte epitope-containing peptide protects against a tumor induced by human papillomavirus type 16-transformed cells.

作者信息

Feltkamp M C, Smits H L, Vierboom M P, Minnaar R P, de Jongh B M, Drijfhout J W, ter Schegget J, Melief C J, Kast W M

机构信息

Department of Immunohematology and Blood bank, University Hospital Leiden, The Netherlands.

出版信息

Eur J Immunol. 1993 Sep;23(9):2242-9. doi: 10.1002/eji.1830230929.

Abstract

Cytotoxic T lymphocyte (CTL) peptide epitopes can be used for immunization of mice against lethal virus infection. To study whether this approach can be successful against virus-induced tumors we generated a B6 (H-2b) tumorigenic cell line transformed by human papillomavirus (HPV). This virus is detected in over 90% of all human cervical cancers. To identify vaccine candidates, we generated a set of 240 overlapping peptides derived from the HPV type 16 (HPV16) oncogenes E6 and E7. These peptides were tested for their ability to bind H-2Kb and H-2Db MHC class I molecules. Binding peptides were compared with the presently known peptide-binding motifs for H-2Kb and H-2Db and the predictive value of these motifs is shortly discussed. The high-affinity H-2Db-binding peptide and putative CTL epitope E7 49-57 (RAHYNIVTF) was used in vaccination studies against HPV 16-transformed tumor cells. Immunization with peptide E7 49-57 rendered mice insensitive to a subsequent challenge with HPV 16-transformed tumor cells in vivo, and induced a CTL response which lysed the tumor cells in vitro.

摘要

细胞毒性T淋巴细胞(CTL)肽表位可用于免疫小鼠以抵抗致死性病毒感染。为了研究这种方法是否能成功对抗病毒诱导的肿瘤,我们构建了一种由人乳头瘤病毒(HPV)转化的B6(H-2b)致瘤细胞系。在所有人类宫颈癌中,超过90%可检测到这种病毒。为了鉴定候选疫苗,我们制备了一组由人乳头瘤病毒16型(HPV16)癌基因E6和E7衍生而来的240个重叠肽。检测了这些肽与H-2Kb和H-2Db I类主要组织相容性复合体(MHC)分子结合的能力。将结合肽与目前已知的H-2Kb和H-2Db肽结合基序进行比较,并简要讨论了这些基序的预测价值。高亲和力的H-2Db结合肽及推定的CTL表位E7 49-57(RAHYNIVTF)被用于针对HPV 16转化肿瘤细胞的疫苗接种研究。用肽E7 49-57免疫可使小鼠在体内对随后HPV 16转化肿瘤细胞的攻击产生抗性,并诱导产生一种能在体外裂解肿瘤细胞的CTL反应。

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