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Systemic neutralizing antibodies induced by long interval mucosally primed systemically boosted immunization correlate with protection from mucosal SHIV challenge

机译:长间隔粘膜引发的全身免疫增强免疫诱导的全身中和抗体与粘膜SHIV攻击的保护相关

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摘要

Immune correlates of vaccine protection from HIV-1 infection would provide important milestones to guide HIV-1 vaccine development. In a proof of concept study using mucosal priming and systemic boosting, the titer of neutralizing antibodies in sera were found to correlate with protection of mucosally exposed rhesus macaques from SHIV infection. Mucosal priming consisted of two sequential immunizations at 12-week intervals with replicating host range mutants of adenovirus type 5 (Ad5hr) expressing the HIV-189.6p env gene. Following boosting with either heterologous recombinant protein or alphavirus replicons at 12-week intervals animals were intrarectally exposed to infectious doses of the CCR5 tropic SHIVSF162p4. Heterologous mucosal prime systemic boost immunization elicited neutralizing antibodies (Nabs), antibody dependent cytotoxicity (ADCC), and specific patterns of antibody binding to envelope peptides. Vaccine induced protection did not correlate with the type of boost nor T-cell responses, but rather with the Nab titer prior to exposure.
机译:疫苗免受HIV-1感染的免疫相关性将为指导HIV-1疫苗的开发提供重要的里程碑。在使用粘膜引发和全身增强的概念验证研究中,发现血清中中和抗体的滴度与保护粘膜暴露的猕猴免受SHIV感染有关。粘膜引发包括以表达HIV-189.6p env基因的5型腺病毒复制宿主范围突变体(Ad5hr)的间隔12周的两次连续免疫。以异源重组蛋白或α病毒复制子加强免疫后,每隔12周对动物进行直肠内暴露于感染剂量的CCR5热带性SHIVSF162p4。异源粘膜初免全身加强免疫引发中和抗体(Nabs),抗体依赖性细胞毒性(ADCC)和抗体与包膜肽结合的特定模式。疫苗诱导的保护与加强免疫或T细胞反应的类型无关,而与暴露前的Nab滴度无关。

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