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嵌合L1-L2病毒样颗粒作为潜在的广谱人乳头瘤病毒疫苗。

Chimeric L1-L2 virus-like particles as potential broad-spectrum human papillomavirus vaccines.

作者信息

Schellenbacher Christina, Roden Richard, Kirnbauer Reinhard

机构信息

Laboratory of Viral Oncology, Division of Immunology, Allergy and Infectious Diseases, Department of Dermatology, Medical University Vienna, Austria.

出版信息

J Virol. 2009 Oct;83(19):10085-95. doi: 10.1128/JVI.01088-09. Epub 2009 Jul 29.

Abstract

The amino (N) terminus of the human papillomavirus (HPV) minor capsid protein L2 can induce low-titer, cross-neutralizing antibodies. The aim of this study was to improve immunogenicity of L2 peptides by surface display on highly ordered, self-assembled virus-like particles (VLP) of major capsid protein L1, and to more completely characterize neutralization epitopes of L2. Overlapping peptides comprising amino acids (aa) 2 to 22 (hereafter, chimera or peptide 2-22), 13 to 107, 18 to 31, 17 to 36, 35 to 75, 75 to 112, 115 to 154, 149 to 175, and 172 to 200 of HPV type 16 (HPV16) L2 were genetically engineered into the DE surface loop of bovine papillomavirus type 1 L1 VLP. Except for chimeras 35-75 and 13-107, recombinant fusion proteins assembled into VLP. Vaccination of rabbits with Freund's adjuvanted native VLP induced higher L2-specific antibody titers than vaccination with corresponding sodium dodecyl sulfate-denatured proteins. Immune sera to epitopes within residues 13 to 154 neutralized HPV16 in pseudovirion neutralization assays, whereas chimera 17-36 induced additional cross-neutralization to divergent high-risk HPV18, -31, -45, -52, and -58; low-risk HPV11; and beta-type HPV5 (titers of 50 to 10,000). Aluminum hydroxide-monophosphoryl lipid A (Alum-MPL)-adjuvanted VLP induced similar patterns of neutralization in both rabbits and mice, albeit with 100-fold-lower titers than Freund's adjuvant. Importantly, Alum-MPL-adjuvanted immunization with chimeric HPV16L1-HPV16L2 (peptide 17-36) VLP induced neutralization or cross-neutralization of HPV16, -18, -31, -45, -52, and -58; HPV6 and -11; and HPV5 (titers of 50 to 100,000). Immunization with HPV16 L1-HPV16 L2 (chimera 17-36) VLP in adjuvant applicable for human use induces broad-spectrum neutralizing antibodies against HPV types evolutionarily divergent to HPV16 and thus may protect against infection with mucosal high-risk, low-risk, and beta HPV types and associated disease.

摘要

人乳头瘤病毒(HPV)次要衣壳蛋白L2的氨基(N)末端可诱导低滴度的交叉中和抗体。本研究的目的是通过在主要衣壳蛋白L1的高度有序、自组装病毒样颗粒(VLP)上进行表面展示来提高L2肽的免疫原性,并更全面地表征L2的中和表位。将包含人乳头瘤病毒16型(HPV16)L2的氨基酸(aa)2至22(以下简称嵌合体或肽2 - 22)、13至107、18至31、17至36、35至75、75至112、115至154、149至175以及172至200的重叠肽基因工程改造到牛乳头瘤病毒1型L1 VLP的DE表面环中。除了嵌合体35 - 75和13 - 107外,重组融合蛋白组装成了VLP。用弗氏佐剂辅助的天然VLP免疫兔子诱导出的L2特异性抗体滴度高于用相应的十二烷基硫酸钠变性蛋白免疫。在假病毒中和试验中,针对残基13至154内表位的免疫血清可中和HPV16,而嵌合体17 - 36诱导了对不同的高危HPV18、- 31、- 45、- 52和- 58;低危HPV11;以及β型HPV5(滴度为50至10,000)的额外交叉中和作用。氢氧化铝 - 单磷酸脂质A(Alum - MPL)佐剂辅助的VLP在兔子和小鼠中诱导出相似的中和模式,尽管滴度比弗氏佐剂低100倍。重要的是,用嵌合HPV16L1 - HPV16L2(肽17 - 36)VLP进行Alum - MPL佐剂免疫诱导了对HPV16、- 18、- 31、- 45、- 52和- 58;HPV6和- 11;以及HPV5(滴度为50至100,000)的中和或交叉中和作用。用适用于人类的佐剂中的HPV16 L1 - HPV16 L2(嵌合体17 - 36)VLP进行免疫可诱导针对与HPV16进化上不同的HPV类型的广谱中和抗体,因此可能预防黏膜高危、低危和β型HPV类型的感染及相关疾病。

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