Baron Michael D, Foster-Cuevas Mildred, Baron Jana, Barrett Thomas
Divisions of Molecular Biology1 and Immunology2, Institute for Animal Health Pirbright Laboratory, Ash Road, Pirbright, Surrey GU24 0NF, UK.
J Gen Virol. 1999 Aug;80 ( Pt 8):2031-2039. doi: 10.1099/0022-1317-80-8-2031.
We have investigated the bovine immune response to heterologous proteins expressed using a recombinant rinderpest virus (RPV). A new gene unit was created in a cDNA copy of the genome of the vaccine strain of RPV, and an open reading frame inserted that encodes the polymerase (3Dpol) and parts of the capsid protein VP1 from foot-and-mouth disease virus (FMDV). Infectious recombinant RPV was rescued and shown to express the FMDV-derived protein at good levels in infected cells. The rescued virus was only slightly more attenuated in tissue culture than the original virus. Cattle infected with this recombinant generated a normal immune response to RPV, and were protected from lethal challenge by that virus. Experimental animals showed a specific delayed-type hypersensitivity response to FMDV 3Dpol, similar to that seen in FMDV infection; however, no antibodies were detected recognizing either of the components of the FMDV-derived protein, nor was any proliferative response to these epitopes found in isolated peripheral blood lymphocytes from infected animals. No protection was seen against FMDV infection.
我们研究了牛对使用重组牛瘟病毒(RPV)表达的异源蛋白的免疫反应。在RPV疫苗株基因组的cDNA拷贝中创建了一个新的基因单元,并插入了一个开放阅读框,该阅读框编码来自口蹄疫病毒(FMDV)的聚合酶(3Dpol)和衣壳蛋白VP1的部分序列。拯救出了具有感染性的重组RPV,并显示其在感染细胞中高水平表达FMDV衍生蛋白。拯救出的病毒在组织培养中的减毒程度仅比原始病毒略高。感染这种重组病毒的牛对RPV产生了正常的免疫反应,并受到该病毒的致死性攻击的保护。实验动物对FMDV 3Dpol表现出特异性迟发型超敏反应,类似于在FMDV感染中观察到的反应;然而,未检测到识别FMDV衍生蛋白任何一种成分的抗体,在感染动物分离的外周血淋巴细胞中也未发现对这些表位的任何增殖反应。未观察到对FMDV感染的保护作用。