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Induction of systemic and mucosal immunity and maintenance of its memory against influenza A virus by nasal vaccination using a new mucosal adjuvant SF-10 derived from pulmonary surfactant in young cynomolgus monkeys

机译:在幼食猕猴中使用新的肺​​表面活性物质黏膜佐剂SF-10进行鼻腔接种,通过鼻疫苗诱导全身和黏膜免疫,并保持其对甲型流感病毒的记忆

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Induction of systemic and mucosal immunity and maintenance of its memory was investigated in 12 young male cynomolgus monkeys after intranasal instillation of flu vaccine using a new mucosal adjuvant SF-10 derived from pulmonary surfactant constituents. Split-product of influenza virus A/Califomia/7/2009(H1N1)pdm hemagglutinin vaccine (HAv) at 15 mu g with or without SF-10 and the adjuvant alone were instilled intranasally three times every 2 weeks. SF-10-adjuvanted HAv (SF-10-HAv) elicited significantly higher HAv-specific IgG and hemagglutinin inhibition (HI) titers in serum and HAv-specific secretory IgA and its neutralizing activities in nasal washes compared with HAv antigen and SF-10 alone. Significant cross-neutralizing activities of nasal washes after the third vaccination to several other H1N1 and H3N2 strains were observed. HI titers in serum and neutralizing activities in nasal washes reached peak levels at 6 weeks after initial vaccination, then gradually decreased after 10 weeks and returned to the baseline levels at 36 weeks. A single intranasal revaccination of SF-10-HAv at 36 weeks rapidly and significantly increased both immunity in serum and nasal washes compared with naive monkeys. Revaccination by one or two doses achieved almost maximal immunity at 2 or 4 weeks after instillation. Statistically significant adverse effects (e.g., body weight loss, elevated body temperature, nasal discharge, change in peripheral blood leukocyte and platelet counts) were not observed for 2 weeks after vaccination of SF-10-HAv, HAv or SF-10 and also during the experimental period. These results in young monkey model suggest the potential of clinical use SF-10 for intranasal flu vaccine. (C) 2016 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license.
机译:在使用来自肺表面活性物质成分的新型粘膜佐剂SF-10鼻内滴注流感疫苗后,在12只雄性食蟹猕猴中研究了诱导全身和粘膜免疫以及维持其记忆的功能。每2周鼻内滴入15毫克含或不含SF-10的流感病毒A / Califomia / 7/2009(H1N1)pdm血凝素疫苗(HAv)的分裂产物。与HAv抗原和SF-10相比,SF-10-佐剂性HAv(SF-10-HAv)在血清和HAv特异性分泌型IgA中引起的HAv特异性IgG和血凝素抑制(HI)滴度明显更高,并且在鼻洗液中具有中和活性单独。观察到第三次接种H1N1和H3N2其他毒株后,鼻洗液具有明显的交叉中和活性。初次接种疫苗后6周,血清HI滴度和鼻洗液的中和活性达到峰值,然后在10周后逐渐降低,并在36周时恢复到基线水平。与幼稚的猴子相比,SF-10-HAv的单次鼻内接种在36周时迅速且显着提高了血清和鼻洗液的免疫力。滴注后2或4周,再接种一剂或两剂可达到几乎最大的免疫力。在接种SF-10-HAv,HAv或SF-10疫苗后2周以及在接种SF-10-HAv,HAv或SF-10后的两周内,均未观察到统计学上显着的不良反应(例如体重减轻,体温升高,鼻分泌物,外周血白细胞和血小板计数的变化)实验期。在幼猴模型中的这些结果表明,SF-10可用于鼻内流感疫苗。 (C)2016作者。由Elsevier Ltd.发布。这是CC BY-NC-ND许可下的开放获取文章。

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