Viral Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Vaccine. 2012 May 9;30(22):3286-94. doi: 10.1016/j.vaccine.2012.03.009. Epub 2012 Mar 15.
The human papillomavirus (HPV) minor capsid protein, L2, is a good candidate for prophylactic vaccine development because L2-specific antibodies have cross-neutralizing activity against diverse HPV types. Here, we developed a HPV mucosal vaccine candidate using the poly-γ-glutamic acid synthetase A (pgsA) protein to display a partial HPV-16 L2 protein (N-terminal 1-224 amino acid) on the surface of Lactobacillus casei (L. casei). The oral immunization with L. casei-L2 induced productions of L2-specific serum IgG and vaginal IgG and IgA in Balb/c mice. To examine cross-neutralizing activity, we used a sensitive high-throughput neutralization assay based on HPV-16, -18, -45, -58, and bovine papillomavirus 1 (BPV1) pseudovirions. Our results revealed that mice vaccinated with L. casei-L2 not only generated neutralizing antibodies against HPV-16, but they also produced antibodies capable of cross-neutralizing the HPV-18, -45, and -58 pseudovirions. Consistent with previous reports, vaccination with HPV-16 L1 virus-like particles (VLPs) failed to show cross-neutralizing activity. Finally, we found that oral administration of L. casei-L2 induced significant neutralizing activities against genital infection by HPV-16, -18, -45, and -58 pseudovirions encoding a fluorescence reporter gene. These results collectively indicate that oral administration of L2 displayed on L. casei induces systemic and mucosal cross-neutralizing effects in mice.
人乳头瘤病毒(HPV)的次要衣壳蛋白 L2 是预防性疫苗开发的良好候选物,因为 L2 特异性抗体对多种 HPV 型具有交叉中和活性。在这里,我们使用多聚γ-谷氨酸合成酶 A(pgsA)蛋白在干酪乳杆菌(L. casei)表面展示 HPV-16 L2 蛋白(N 端 1-224 个氨基酸),开发了一种 HPV 黏膜疫苗候选物。用 L. casei-L2 进行口服免疫可诱导 Balb/c 小鼠产生 L2 特异性血清 IgG 和阴道 IgG 和 IgA。为了检测交叉中和活性,我们使用了一种基于 HPV-16、-18、-45、-58 和牛乳头瘤病毒 1(BPV1)假病毒的灵敏高通量中和测定法。我们的结果表明,用 L. casei-L2 免疫的小鼠不仅产生了针对 HPV-16 的中和抗体,而且还产生了能够中和 HPV-18、-45 和 -58 假病毒的抗体。与之前的报告一致,HPV-16 L1 病毒样颗粒(VLPs)的免疫接种未能显示出交叉中和活性。最后,我们发现,L. casei-L2 的口服给药可诱导针对 HPV-16、-18、-45 和 -58 假病毒(编码荧光报告基因)引起的生殖器感染的显著中和活性。这些结果共同表明,L. casei 上展示的 L2 的口服给药可在小鼠中诱导系统和黏膜交叉中和作用。