Division of Mucosal Vaccines, International Research and Development Center for Mucosal Vaccine, The Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan; Department of Mucosal Immunology, IMSUT Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan.
Division of Mucosal Vaccines, International Research and Development Center for Mucosal Vaccine, The Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan.
Vaccine. 2021 Jun 8;39(25):3353-3364. doi: 10.1016/j.vaccine.2021.04.069. Epub 2021 May 17.
Current polysaccharide-based pneumococcal vaccines are effective but not compatible with all serotypes of Streptococcus pneumoniae. We previously developed an adjuvant-free cationic nanogel nasal vaccine containing pneumococcal surface protein A (PspA), which is expressed on the surfaces of all pneumococcal serotypes. Here, to address the sequence diversity of PspA proteins, we formulated a cationic nanogel-based trivalent pneumococcal nasal vaccine and demonstrated the vaccine's immunogenicity and protective efficacy in macaques by using a newly developed nasal spray device applicable to humans. Nasal vaccination of macaques with cationic cholesteryl pullulan nanogel (cCHP)-trivalent PspA vaccine effectively induced PspA-specific IgGs that bound to pneumococcal surfaces and triggered complement C3 deposition. The immunized macaques were protected from pneumococcal intratracheal challenge through both inhibition of lung inflammation and a dramatic reduction in the numbers of bacteria in the lungs. These results demonstrated that the cCHP-trivalent PspA vaccine is an effective candidate vaccine against pneumococcal infections.
目前基于多糖的肺炎球菌疫苗具有疗效,但不能与所有血清型的肺炎链球菌相匹配。我们之前开发了一种不含佐剂的阳离子纳米凝胶鼻用疫苗,其中含有肺炎球菌表面蛋白 A(PspA),该蛋白存在于所有肺炎球菌血清型的表面。在这里,为了解决 PspA 蛋白的序列多样性问题,我们设计了一种基于阳离子纳米凝胶的三价肺炎球菌鼻用疫苗,并通过使用新开发的适用于人类的鼻腔喷雾装置,在猕猴中证明了该疫苗的免疫原性和保护效力。用阳离子胆甾醇 pullulan 纳米凝胶(cCHP)-三价 PspA 疫苗对猕猴进行鼻腔接种,可有效诱导与肺炎球菌表面结合并触发补体 C3 沉积的 PspA 特异性 IgG。免疫接种的猕猴通过抑制肺部炎症和肺部细菌数量的大量减少,从而免受肺炎球菌气管内攻击的侵害。这些结果表明,cCHP-三价 PspA 疫苗是一种针对肺炎球菌感染的有效候选疫苗。