首页> 美国卫生研究院文献>Journal of Virology >Protection of Rabbits against Challenge with Rabbit Papillomaviruses by Immunization with the N Terminus of Human Papillomavirus Type 16 Minor Capsid Antigen L2
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Protection of Rabbits against Challenge with Rabbit Papillomaviruses by Immunization with the N Terminus of Human Papillomavirus Type 16 Minor Capsid Antigen L2

机译:通过用人乳头瘤病毒16型小衣壳抗原L2的N末端免疫接种来保护兔免受兔乳头瘤病毒的攻击。

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摘要

Current L1 virus-like particle (VLP) vaccines provide type-restricted protection against a small subset of the human papillomavirus (HPV) genotypes associated with cervical cancer, necessitating continued cytologic screening of vaccinees. Cervical cancer is most problematic in countries that lack the resources for screening or highly multivalent HPV VLP vaccines, suggesting the need for a low-cost, broadly protective vaccinogen. Here, N-terminal L2 polypeptides comprising residues 1 to 88 or 11 to 200 derived from HPV16, bovine papillomavirus type 1 (BPV1), or cottontail rabbit papillomavirus (CRPV) were produced in bacteria. Rabbits were immunized with these N-terminal L2 polypeptides and concurrently challenged with CRPV and rabbit oral papillomavirus (ROPV). Vaccination with either N-terminal L2 polypeptides of CRPV effectively protected rabbits from CRPV challenge but not from papillomas induced by cutaneous challenge with CRPV genomic DNA. Furthermore, papillomas induced by CRPV genomic DNA deficient for L2 expression grew at the same rate as those induced by wild-type CRPV genomic DNA, further suggesting that the L2 polypeptide vaccines lack therapeutic activity. Neutralizing serum antibody titers of >15 correlated with protection (P < 0.001), a finding consistent with neutralizing antibody-mediated protection. Surprisingly, a remarkable degree of protection against heterologous papillomavirus types was observed after vaccination with N-terminal L2 polypeptides. Notably, vaccination with HPV16 L2 11-200 protected against cutaneous and mucosal challenge with CRPV and ROPV, respectively, papillomaviruses that are evolutionarily divergent from HPV16. Further, vaccination with HPV16 L2 11-200 generates broadly cross-neutralizing serum antibody, suggesting the potential of L2 as a second-generation preventive HPV vaccine antigen.
机译:当前的L1病毒样颗粒(VLP)疫苗针对与宫颈癌相关的一小部分人乳头瘤病毒(HPV)基因型提供了类型限制的保护,因此需要继续进行疫苗的细胞学筛选。在缺乏筛查资源或高度多价HPV VLP疫苗的国家中,宫颈癌的问题最为严重,这表明需要低成本,广泛保护的疫苗原。在此,在细菌中产生了包含源自HPV16、1型牛乳头瘤病毒(BPV1)或棉尾兔乳头瘤病毒(CRPV)的残基1至88或11至200的N末端L2多肽。用这些N末端L2多肽免疫兔,并同时用CRPV和兔口服乳头瘤病毒(ROPV)攻击。用CRPV的N端L2多肽进行疫苗接种可有效地保护兔子免受CRPV攻击,但不能免受因CRPV基因组DNA皮肤刺激引起的乳头状瘤。此外,由缺乏L2表达的CRPV基因组DNA诱导的乳头状瘤以与由野生型CRPV基因组DNA诱导的乳头状瘤相同的速率生长,进一步表明L2多肽疫苗缺乏治疗活性。大于15的中和血清抗体滴度与保护作用相关(P <0.001),这一发现与中和抗体介导的保护作用一致。出人意料的是,在用N-末端L2多肽接种后观察到显着程度的针对异源乳头瘤病毒类型的保护。值得注意的是,用HPV16 L2 11-200进行的疫苗接种分别针对CRPV和ROPV抵御了从HPV16进化分化出的乳头瘤病毒,防止皮肤和粘膜攻击。此外,用HPV16 L2 11-200进行疫苗接种可产生广泛的交叉中和血清抗体,这表明L2作为第二代预防性HPV疫苗抗原的潜力。

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