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首页> 外文期刊>Infection and immunity >DNA Vaccines Expressing a Fusion Product of Outer Surface Proteins A and C from Borrelia burgdorferi Induce Protective Antibodies Suitable for Prophylaxis but Not for Resolution of Lyme Disease
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DNA Vaccines Expressing a Fusion Product of Outer Surface Proteins A and C from Borrelia burgdorferi Induce Protective Antibodies Suitable for Prophylaxis but Not for Resolution of Lyme Disease

机译:表达来自伯氏疏螺旋体的外表面蛋白A和C融合产物的DNA疫苗诱导出适用于预防但不解决莱姆病的保护性抗体

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DNA vaccines encoding the outer surface protein A (OspA) ofBorrelia burgdorferi have been shown to induce protective humoral responses capable of preventing but not curing infection in mice. Subsequent studies showed that an established infection or disease could be resolved by passive transfer of antibodies to OspC. In the present study, DNA vaccines encoding either the OspC antigen alone or fused to OspA and under the transcriptional control of the human elongation factor 1α promoter were evaluated for their protective and/or curative potential. In contrast to ospA-containing plasmids, none of the six constructs with ospC alone were immunogenic in vivo, independent of whether they contained promoter or leader sequences from ospA and/or ospC, or alternatively, the signal sequence of the human tissue plasminogen activator. Solely, a DNA vaccine encoding an OspA-OspC fusion product led to expression of the respective polypeptide chain in transfected cells in vitro and to the induction of OspA- and OspC-specific antibodies in vivo. Immune sera raised against the OspA-OspC fusion product conveyed full protection against subsequent infection, most probably via OspA-specific antibodies, but were unable to resolve infection.
机译:已经证明,编码伯氏疏螺旋体的外表面蛋白A(OspA)的DNA疫苗可诱导保护性体液反应,这种反应可预防但不能治愈小鼠感染。随后的研究表明,可以通过将抗体被动转移至OspC来解决已确定的感染或疾病。在本研究中,评估了编码单独的OspC抗原或与OspA融合并在人类延伸因子1α启动子的转录控制下编码的DNA疫苗的保护和/或治疗潜力。与含 ospA 的质粒相反,六个单独含 ospC 的构建体在体内均无免疫原性,与它们是否包含来自 ospA < / em>和/或 ospC ,或人类组织纤溶酶原激活剂的信号序列。唯一地,编码OspA-OspC融合产物的DNA疫苗导致体外转染的细胞中相应多肽链的表达,并导致体内OspA和OspC特异性抗体的诱导。针对OspA-OspC融合产物产生的免疫血清可提供针对随后感染的全面保护,最有可能是通过OspA特异性抗体,但无法解决感染。

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