Laboratorio de Inmunología y Virología, Departamento de Ciencia y Tecnología, Universidad Nacional de Quilmes, Roque Sáenz Peña 352, Bernal, 1876, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Godoy Cruz 2290, Ciudad Autónoma de Buenos Aires, 1425, Argentina.
Instituto de Estudios Inmunológicos y Fisiopatológicos (IIFP), Facultad de Ciencias Exactas, Universidad Nacional de La Plata - Consejo Nacional de Investigaciones Científicas y Técnicas (UNLP-CONICET), Boulevard 120 1489, La Plata, 1900, Argentina.
J Pharm Sci. 2024 Jul;113(7):1794-1803. doi: 10.1016/j.xphs.2024.03.013. Epub 2024 Mar 22.
Research on innovative mucosal adjuvants is essential to develop new vaccines for safe mucosal application. In this work, we propose the development of a Lactococcus lactis that expresses a variant of flagellin on its surface (FliC131*), to increase the adjuvanticity of the living cell and cell wall-derived particles (CWDP). We optimized the expression of FliC131*, and confirmed its identity and localization by Western blot and flow cytometry. We also generated CWDP containing FliC131* (CDWP-FliC131*) and evaluated their storage stability. Lastly, we measured the human TLR5 stimulating activity in vitro and assessed the adjuvanticity in vivo using ovalbumin (OVA) as a model antigen. As a result, we generated L. lactis/pCWA-FliC131*, that expresses and displays FliC131* on its surface, obtained the corresponding CWDP-FliC131*, and showed that both activated hTLR5 in vitro in a dose-dependent manner. Furthermore, CWDP-FliC131* retained this biological activity after being lyophilized and stored for a year. Finally, intranasal immunization of mice with OVA plus live L. lactis/pCWA-FliC131* or CWDP-FliC131* induced OVA-specific IgG and IgA in serum, intestinal lavages, and bronchoalveolar lavages. Our work demonstrates the potential of this recombinant L. lactis with an enhanced adjuvant effect, prompting its further evaluation for the design of novel mucosal vaccines.
研究创新型黏膜佐剂对于开发安全的黏膜应用新疫苗至关重要。在这项工作中,我们提出了一种在表面表达鞭毛蛋白变体(FliC131*)的乳球菌的开发,以提高活细胞和细胞壁衍生颗粒(CWDP)的佐剂活性。我们优化了 FliC131的表达,并通过 Western blot 和流式细胞术确认了其身份和定位。我们还生成了含有 FliC131的 CWDP(CDWP-FliC131*),并评估了它们的储存稳定性。最后,我们在体外测量了人 TLR5 刺激活性,并使用卵清蛋白(OVA)作为模型抗原评估了体内的佐剂活性。结果,我们生成了表达和表面展示 FliC131的 L. lactis/pCWA-FliC131,获得了相应的 CWDP-FliC131*,并表明两者均以剂量依赖性方式在体外激活 hTLR5。此外,CWDP-FliC131在冻干并储存一年后仍保留这种生物学活性。最后,用 OVA 加活 L. lactis/pCWA-FliC131或 CWDP-FliC131*经鼻腔免疫小鼠诱导了血清、肠灌洗液和支气管肺泡灌洗液中的 OVA 特异性 IgG 和 IgA。我们的工作证明了这种具有增强佐剂作用的重组乳球菌的潜力,促使其进一步评估用于设计新型黏膜疫苗。