Schellenbacher Christina, Roden Richard, Kirnbauer Reinhard
Laboratory of Viral Oncology, Division of Immunology, Allergy and Infectious Diseases, Department of Dermatology, Medical University Vienna, Austria.
J Virol. 2009 Oct;83(19):10085-95. doi: 10.1128/JVI.01088-09. Epub 2009 Jul 29.
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.
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。