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新型豚鼠特异性干扰素-γ酶联免疫斑点试验的开发以及用安卡拉痘苗病毒(MVA)载体GP83疫苗免疫后豚鼠巨细胞病毒GP83特异性细胞免疫反应的特征分析

Development of a novel, guinea pig-specific IFN-γ ELISPOT assay and characterization of guinea pig cytomegalovirus GP83-specific cellular immune responses following immunization with a modified vaccinia virus Ankara (MVA)-vectored GP83 vaccine.

作者信息

Gillis Peter A, Hernandez-Alvarado Nelmary, Gnanandarajah Josephine S, Wussow Felix, Diamond Don J, Schleiss Mark R

机构信息

University of Minnesota Medical School, Department of Pediatrics, Center for Infectious Diseases and Microbiology Translational Research, 2001 6th Street SE, Minneapolis, MN 55455, United States.

Department of Virology, Beckman Research Institute of City of Hope, 1500 E. Duarte Road, Duarte, CA 91010, United States.

出版信息

Vaccine. 2014 Jun 30;32(31):3963-70. doi: 10.1016/j.vaccine.2014.05.011. Epub 2014 May 20.

Abstract

The guinea pig (Cavia porcellus) provides a useful animal model for studying the pathogenesis of many infectious diseases, and for preclinical evaluation of vaccines. However, guinea pig models are limited by the lack of immunological reagents required for characterization and quantification of antigen-specific T cell responses. To address this deficiency, an enzyme-linked immunospot (ELISPOT) assay for guinea pig interferon (IFN)-γ was developed to measure antigen/epitope-specific T cell responses to guinea pig cytomegalovirus (GPCMV) vaccines. Using splenocytes harvested from animals vaccinated with a modified vaccinia virus Ankara (MVA) vector encoding the GPCMV GP83 (homolog of human CMV pp65 [gpUL83]) protein, we were able to enumerate and map antigen-specific responses, both in vaccinated as well as GPCMV-infected animals, using a panel of GP83-specific peptides. Several potential immunodominant GP83-specific peptides were identified, including one epitope, LGIVHFFDN, that was noted in all guinea pigs that had a detectable CD8+ response to GP83. Development of a guinea pig IFN-γ ELISPOT should be useful in characterization of additional T cell-specific responses to GPCMV, as well as other pathogens. This information in turn can help focus future experimental evaluation of immunization strategies, both for GPCMV as well as for other vaccine-preventable illnesses studied in the guinea pig model.

摘要

豚鼠(Cavia porcellus)为研究多种传染病的发病机制以及疫苗的临床前评估提供了一种有用的动物模型。然而,豚鼠模型受到表征和定量抗原特异性T细胞反应所需免疫试剂缺乏的限制。为了解决这一缺陷,开发了一种用于豚鼠干扰素(IFN)-γ的酶联免疫斑点(ELISPOT)检测方法,以测量对豚鼠巨细胞病毒(GPCMV)疫苗的抗原/表位特异性T细胞反应。使用从接种编码GPCMV GP83(人巨细胞病毒pp65 [gpUL83]的同源物)蛋白的改良安卡拉痘苗病毒(MVA)载体的动物中收获的脾细胞,我们能够使用一组GP83特异性肽来计数和绘制接种疫苗以及感染GPCMV的动物中的抗原特异性反应。鉴定出了几种潜在的免疫显性GP83特异性肽,包括一个表位LGIVHFFDN,在所有对GP83有可检测到的CD8 +反应的豚鼠中都观察到了该表位。豚鼠IFN-γ ELISPOT的开发对于表征对GPCMV以及其他病原体的额外T细胞特异性反应应该是有用的。反过来,这些信息可以帮助聚焦未来对免疫策略的实验评估,无论是针对GPCMV还是在豚鼠模型中研究的其他疫苗可预防疾病。

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