Department of Biophysics and Structural Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, School of Basic Medicine Peking Union Medical College, Beijing, China.
The Fifth Department of Biological Products, Institute of Medical Biology, Chinese Academy of Medical Science, Peking Union Medical College, Yunnan, China.
J Med Virol. 2020 Dec;92(12):3750-3758. doi: 10.1002/jmv.25690. Epub 2020 Feb 19.
Sequential immunization with antigens from different strains of HIV-1, influenza viruses or dengue viruses induced cross-neutralizing antibodies and enhanced the antibody responses against previous antigens. The characteristics of neutralizing antibodies induced by sequential immunization with different types of human papillomavirus (HPV) L1 virus-like particles (L1VLPs) are unclear. In this study, mice were primed with one or two types (HPV-16 or HPV16/18) of L1VLPs, then boosted sequentially with HPV6/18/45/11/31/58 or HPV6/45/11/31/58 L1VLPs, and sera were analyzed with HPV pseudovirus-based neutralization assay. The results showed that neutralizing activities against earlier immunized vaccine types were enhanced gradually by subsequent immunizations, and low levels of neutralizing activities against nonvaccine types (HPV33/35/52/59/68) were also observed. After absorbing the immune sera with vaccine-type (HPV16/18/45) L1VLPs, neutralizing activities against tested priming and boosting types (HPV16/18/58) decreased significantly, and that against nonvaccine type (HPV-33) was also partially eliminated. Moreover, neutralizing activities against vaccine types (HPV16/58) were significantly reduced after absorbing with nonvaccine-type VLPs (HPV33/52). These data suggest that cross-neutralizing epitopes exist among different HPV L1VLPs. The cross-neutralizing activities against nonvaccine types and the enhanced neutralizing activities against earlier immunized vaccine types may result from sequential boosting with these cross-neutralizing epitopes. These observations support early vaccination with more types of L1VLPs derived from HPVs that cause a serious threat to the population.
先后免疫不同株 HIV-1、流感病毒或登革热病毒的抗原可诱导交叉中和抗体,并增强针对先前抗原的抗体应答。先后免疫不同类型的人乳头瘤病毒(HPV)L1 病毒样颗粒(L1VLPs)所诱导的中和抗体的特征尚不清楚。在这项研究中,用一种或两种类型(HPV-16 或 HPV16/18)的 L1VLPs 对小鼠进行初免,然后先后用 HPV6/18/45/11/31/58 或 HPV6/45/11/31/58 L1VLPs 进行加强免疫,并用 HPV 假病毒中和试验分析血清。结果表明,后续免疫逐渐增强了对早期免疫疫苗类型的中和活性,并且还观察到对非疫苗类型(HPV33/35/52/59/68)的低水平中和活性。用疫苗型(HPV16/18/45)L1VLPs 吸收免疫血清后,对测试的初免和加强型(HPV16/18/58)的中和活性显著降低,对非疫苗型(HPV-33)的中和活性也部分消除。此外,用非疫苗型 VLPs(HPV33/52)吸收后,对疫苗型(HPV16/58)的中和活性显著降低。这些数据表明,不同 HPV L1VLPs 之间存在交叉中和表位。对非疫苗类型的交叉中和活性以及对早期免疫疫苗类型的增强中和活性可能是由于这些交叉中和表位的先后加强免疫引起的。这些观察结果支持对人群构成严重威胁的 HPV 用更多类型的 L1VLPs 进行早期接种。