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Suppression of Immune Response to Adenovirus Serotype 5 Vector by Immunization with Peptides Containing an MHC Class II Epitope and a Thio-Oxidoreductase Motif

机译:通过免疫含有II类MHC抗原决定簇和硫代氧化还原酶基序的肽,抑制对5型腺病毒载体的免疫反应。

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摘要

The main obstacle to viral vector-mediated gene therapy remains the elicitation of an immune response to the vector, resulting in clearance of transgene and resistance to further transgenesis. Specific antibody production contributes to such immune responses. A single class II-restricted epitope of adenovirus serotype 5 (Ad5) vector hexon-6 capsid protein containing a thiol-oxidoreductase motif was used in an attempt to prevent specific antibody production in response to Ad5 vectors. We demonstrate here that such immunization carried out before intravenous administration of Ad5 vectors prevents antibody production to the ensemble of Ad5 vector proteins in both BALB/c and C57BL/6 mice. The antibody response to Ad5 is dependent on innate immune activation, seemingly involving natural killer T (NKT) cells. We observed that immunization with a class II-restricted Ad5 peptide prevents such NKT cell activation. Increased transgenesis and prolonged transgene expression result from such immunization, providing a simple protocol for improving gene therapy.
机译:病毒载体介导的基因治疗的主要障碍仍然是引发对载体的免疫反应,从而导致转基因的清除和对进一步转基因的抗性。特异性抗体的产生有助于这种免疫应答。为了防止针对Ad5载体的特异性抗体产生,使用了含有硫醇-氧化还原酶基序的腺病毒血清型5(Ad5)载体六邻体6衣壳蛋白的单一II类限制性表位。我们在这里证明,在静脉内施用Ad5载体之前进行的此类免疫可防止在BALB / c和C57BL / 6小鼠体内抗体产生至Ad5载体蛋白的整体。对Ad5的抗体反应取决于先天免疫激活,似乎涉及自然杀伤T(NKT)细胞。我们观察到,用II类限制性Ad5肽免疫可防止此类NKT细胞激活。这种免疫导致转基因增加和转基因表达延长,从而为改善基因治疗提供了简单的方案。

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