Zhu Wandi, Pewin Winston, Wang Chao, Luo Yuan, Gonzalez Gilbert X, Mohan Teena, Prausnitz Mark R, Wang Bao-Zhong
Center for Inflammation, Immunity & Infection, Georgia State University Institute for Biomedical Sciences, Atlanta, GA 30303, USA.
School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.
J Control Release. 2017 Sep 10;261:1-9. doi: 10.1016/j.jconrel.2017.06.017. Epub 2017 Jun 19.
The biodegradable microneedle patch (MNP) is a novel technology for vaccine delivery that could improve the immunogenicity of vaccines. To broaden the protective efficiency of conventional influenza vaccines, a new 4M2e-tFliC fusion protein construct containing M2e sequences from different subtypes was generated. Purified fusion protein was encapsulate into MNPs with a biocompatible polymer for use as a boosting vaccine. The results demonstrated that mice receiving a conventional inactivated vaccine followed by a skin-applied dissolving 4M2e-tFliC MNP boost could better maintain the humoral antibody response than that by the conventional vaccine-prime alone. Compared with an intramuscular injection boost, mice receiving the MNP boost showed significantly enhanced cellular immune responses, hemagglutination-inhibition (HAI) titers, and neutralization titers. Increased frequency of antigen-specific plasma cells and long-lived bone marrow plasma cells was detected in the MNP boosted group as well, indicating that skin vaccination with 4M2e-tFliC facilitated a long-term antibody-mediated immunity. The 4M2e-tFliC MNP-boosted group also possessed enhanced protection against high lethal dose challenges against homologous A/PR/8/34 and A/Aichi/2/68 viruses and protection for a majority of immunized mice against a heterologous A/California/07/2009 H1N1 virus. High levels of M2e specific immune responses were observed in the 4M2e-tFliC MNP-boosted group as well. These results demonstrate that a skin-applied 4M2e-tFliC MNP boosting immunization to seasonal vaccine recipients may be a rapid approach for increasing the protective efficacy of seasonal vaccines in response to a significant drift seen in circulating viruses. The results also provide a new perspective for future exploration of universal influenza vaccines.
可生物降解微针贴片(MNP)是一种用于疫苗递送的新技术,可提高疫苗的免疫原性。为了扩大传统流感疫苗的保护效果,构建了一种新的包含来自不同亚型M2e序列的4M2e-tFliC融合蛋白。将纯化的融合蛋白用生物相容性聚合物封装到微针贴片中,用作加强疫苗。结果表明,先接受传统灭活疫苗,随后经皮肤接种可溶解的4M2e-tFliC微针贴片加强免疫的小鼠,与仅接受传统疫苗初免相比,能更好地维持体液抗体反应。与肌肉注射加强免疫相比,接受微针贴片加强免疫的小鼠表现出显著增强的细胞免疫反应、血凝抑制(HAI)效价和中和效价。在微针贴片加强免疫组中也检测到抗原特异性浆细胞和长寿骨髓浆细胞的频率增加,这表明用4M2e-tFliC进行皮肤疫苗接种促进了长期的抗体介导免疫。4M2e-tFliC微针贴片加强免疫组对同源A/PR/8/34和A/爱知/2/68病毒的高致死剂量攻击也具有增强的保护作用,并且对大多数免疫小鼠具有针对异源A/加利福尼亚/07/2009 H1N1病毒的保护作用。在4M2e-tFliC微针贴片加强免疫组中也观察到高水平的M2e特异性免疫反应。这些结果表明,对季节性疫苗接种者进行经皮肤的4M2e-tFliC微针贴片加强免疫可能是一种快速提高季节性疫苗保护效果的方法,以应对流行病毒中出现的显著抗原漂移。这些结果也为未来通用流感疫苗的探索提供了新的视角。