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Multiple Antigenic Peptide-Based Vaccines Targeting Ixodes ricinus Neuropeptides Induce a Specific Antibody Response but Do Not Impact Tick Infestation

机译:靶向Ixodes患者的多种抗原肽的疫苗诱导特异性抗体反应,但不会影响蜱灭绝

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摘要

Synthetic peptide vaccines were designed to target the neuropeptides innervating Ixodes ricinus salivary glands and hindgut and they were tested for their capacity to afford protective immunity against nymphs or larvae and Anaplasma phagocytophilum-infected nymph infestation, in mice and sheep, respectively. In both models, the assembly of SIFamide (SIFa) or myoinhibitory peptide (MIP) neuropeptides into multiple antigenic peptide constructs (MAPs) elicited a robust IgG antibody response following immunization. Nevertheless, no observable detrimental impact on nymphs was evidenced in mice, and, unfortunately, the number of engorged nymphs on sheep was insufficient for firm conclusions to be drawn, including for bacterial transmission. Regarding larvae, while vaccination of the sheep did not globally diminish tick feeding success or development, analyses of animals at the individual level revealed a negative correlation between anti-SIFa and MIP antibody levels and larva-to-nymph molting success for both antigens. Our results provide a proof of principle and precedent for the use of MAPs for the induction of immunity against tick peptide molecules. Although the present study did not provide the expected level of protection, it inaugurates a new strategy for protection against ticks based on the immunological targeting of key components of their nervous system.
机译:设计了合成肽疫苗以靶向神经肽的神经肽,其中患有含有肝唾液腺和后肠,它们分别测试其能力,以分别为小鼠和绵羊的患有针对若虫的保护性免疫和Anaplasma吞噬细胞感染的若虫感染的若虫感染。在两种模型中,将SiFAMIDE(SIFA)或肌抑制肽(MIP)神经肽的组装成多种抗原肽构建体(MAPS)引发了免疫接种后的鲁棒IgG抗体反应。尽管如此,小鼠没有可观察到对若虫的有害影响,并且不幸的是,绵羊上绿色若虫的数量不足以得出结论,包括细菌传播。关于幼虫,而绵羊的疫苗接种没有全球减少蜱喂养成功或发育,在各个水平的动物分析揭示了抗SiFA和MIP抗体水平和幼虫对抗原的幼虫成功的负相关。我们的结果提供了原则上的证据和先例,用于使用地图用于诱导蜱肽分子的免疫。虽然本研究没有提供预期的保护水平,但它揭示了一种基于神经系统关键组分的免疫靶向保护的新策略。

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