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Displaying 31RG-1 peptide on the surface of HPV16 L1 by use of a human papillomavirus chimeric virus-like particle induces cross-neutralizing antibody responses in mice

机译:通过使用人乳头瘤病毒嵌合病毒样颗粒在HPV16 L1表面上显示31RG-1肽在小鼠中诱导交叉中和抗体反应

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摘要

Current available human papillomavirus (HPV) vaccines are based on the major capsid protein L1 virus-like particles (VLPs), which mainly induce type-specific neutralizing antibodies against vaccine types. Continuing to add more types of VLPs in a vaccine raises the complexity and cost of production which remains the principal impediment to achieve broad implementation of HPV vaccines, particularly in developing regions. In this study, we constructed 16L1-31L2 chimeric VLP (cVLP) by displaying HPV31 L2 aa.17-38 on the h4 coil surface region of HPV16 L1, and assessed its immunogenicity in mouse model. We found that the cVLP adjuvanted with alum plus monophosphoryl lipid A could induce cross-neutralizing antibody responses against 16 out of 17 tested HPV pseudoviruses, and the titer against HPV16 was as high as that was induced by HPV16 L1VLP (titer 10(5)), more importantly, titers over 10 3 were observed against two HR-HPVs including HPV31 (titer, 2,200) and -59 (titer, 1,013), among which HPV59 was not covered by Gardasil-9, and medium or low titers of cross-neutralizing antibodies against other 13 tested HPV pseudoviruses were also observed. Our data demonstrate that 16L1-31L2 cVLP is a promising candidate for the formulation of broader spectrum HPV vaccines.
机译:目前可用的人乳头瘤病毒(HPV)疫苗基于主要的衣壳样蛋白L1病毒样颗粒(VLP),其主要诱导特异性中和抗体免受疫苗类型的抗体。继续在疫苗中添加更多类型的VLP提高了生产的复杂性和成本,仍然是实现HPV疫苗的广泛实施的主要障碍,特别是在发展中地。在该研究中,我们通过在HPV16L1的H4线圈表面区域上显示HPV31 L2 AA.17-38构建16L1-31L2嵌合VLP(CVLP),并评估其小鼠模型中的免疫原性。我们发现,用alum加单磷酸脂质A佐剂辅助的CVLP可以诱导与17个测试的HPV伪病毒中的16种的交叉中和抗体反应,并且反对HPV16的滴度高于HPV16 L1VLP诱导的滴度(Titer≫ 10(5)更重要的是,更重要的是,针对包括HPV31(滴度,2,200)和-59(滴度,1,013)的两个HR-HPV观察到超过10 3的滴度,其中HPV59未被Gardasil-9和中等或低滴度覆盖还观察到对其他13个测试的HPV假纲病毒的交叉中和抗体。我们的数据表明,16L1-31L2 CVLP是制定更广谱HPV疫苗的有希望的候选者。

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