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在HLA - A2.1转基因兔模型中,用E1多价表位DNA疫苗对棉尾兔乳头瘤病毒(CRPV)感染的保护性免疫。

Protective immunity with an E1 multivalent epitope DNA vaccine against cottontail rabbit papillomavirus (CRPV) infection in an HLA-A2.1 transgenic rabbit model.

作者信息

Hu Jiafen, Cladel Nancy, Peng Xuwen, Balogh Karla, Christensen Neil D

机构信息

Jake Gittlen Cancer Research Foundation, Department of Pathology, Pennsylvania State University college of medicine, Hershey, PA 17033, USA.

出版信息

Vaccine. 2008 Feb 6;26(6):809-16. doi: 10.1016/j.vaccine.2007.11.081. Epub 2007 Dec 26.

Abstract

Cottontail rabbit papillomavirus (CRPV)/rabbit model is widely used to study pathogenesis of papillomavirus infections and malignant tumor progression. Recently, we established HLA-A2.1 transgenic rabbit lines and demonstrated efficacy for the testing of immunogenicity of a well-known A2-resticted epitope (HPV16E7/82-90) [Hu J, Peng X, Schell TD, Budgeon LR, Cladel NM, Christensen ND. An HLA-A2.1-transgenic rabbit model to study immunity to papillomavirus infection. J Immunol 2006;177(11):8037-45]. In the present study, we screened five HLA-A2.1 restricted epitopes from CRPVE1 (selected using online MHCI epitope prediction software) and constructed a multivalent epitope DNA vaccine (CRPVE1ep1-5). CRPVE1ep1-5 and a control DNA vaccine (Ub3) were then delivered intracutaneously onto normal and HLA-A2.1 transgenic rabbits, respectively, by a helium-driven gene-gun delivery system. One, two or three immunizations were given to different groups of animals from both New Zealand White outbred and EIII/JC inbred genetic background. Two and three immunizations with CRPVE1ep1-5 DNA vaccine provided complete protection against viral DNA infection of HLA-A2.1 transgenic rabbits from both genetic backgrounds but not in the control-vaccinated groups. One immunization, however, failed to protect HLA-A2.1 transgenic rabbits against viral DNA infection. This study further demonstrated that the HLA-A2.1 transgenic rabbits can be used to test the immunogenicity of HLA-A2.1 restricted epitopes identified by MHCI epitope predication software.

摘要

棉尾兔乳头瘤病毒(CRPV)/兔模型被广泛用于研究乳头瘤病毒感染的发病机制和恶性肿瘤进展。最近,我们建立了HLA - A2.1转基因兔品系,并证明了其在测试一种著名的A2限制性表位(HPV16E7/82 - 90)免疫原性方面的有效性[胡J,彭X,谢尔TD,布金LR,克拉德尔NM,克里斯蒂安森ND。一种用于研究对乳头瘤病毒感染免疫的HLA - A2.1转基因兔模型。《免疫学杂志》2006;177(11):8037 - 45]。在本研究中,我们从CRPV E1中筛选了五个HLA - A2.1限制性表位(使用在线MHCI表位预测软件选择),并构建了一种多价表位DNA疫苗(CRPVE1ep1 - 5)。然后,通过氦驱动基因枪递送系统,将CRPVE1ep1 - 5和一种对照DNA疫苗(Ub³)分别皮内递送至正常兔和HLA - A2.1转基因兔。对来自新西兰白兔远交系和EIII/JC近交系遗传背景的不同动物组进行了一次、两次或三次免疫。用CRPVE1ep1 - 5 DNA疫苗进行两次和三次免疫可使来自两种遗传背景的HLA - A2.1转基因兔完全免受病毒DNA感染,但对照疫苗接种组则不能。然而,一次免疫未能保护HLA - A2.1转基因兔免受病毒DNA感染。本研究进一步证明,HLA - A2.1转基因兔可用于测试通过MHCI表位预测软件鉴定的HLA - A2.1限制性表位的免疫原性。

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