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预先存在的中和抗体对嵌合人乳头瘤病毒样颗粒疫苗诱导的抗肿瘤免疫反应的影响。

Effect of preexisting neutralizing antibodies on the anti-tumor immune response induced by chimeric human papillomavirus virus-like particle vaccines.

作者信息

Da Silva D M, Pastrana D V, Schiller J T, Kast W M

机构信息

Cancer Immunology Program, Cardinal Bernardin Cancer Center, Department of Microbiology and Immunology, Loyola University Chicago, 2160 South First Avenue, Maywood, Illinois 60153, USA.

出版信息

Virology. 2001 Nov 25;290(2):350-60. doi: 10.1006/viro.2001.1179.

DOI:10.1006/viro.2001.1179
PMID:11883199
Abstract

Chimeric human papillomavirus virus-like particles (HPV cVLPs) carrying HPV16 E7 protein are potent vaccines for inducing cell-mediated immunity (CMI) against HPV-induced tumors in animal models. We tested the hypothesis that virion-neutralizing antibodies generated during an initial vaccination might prevent effective boosting of CMI to the cVLPs. Mice with circulating HPV16-neutralizing antibodies, generated by direct immunization with wild-type VLPs or by passive transfer of hyperimmune anti-HPV16 VLP mouse sera, were subsequently vaccinated with HPV16 E7-containing cVLPs. Mice with preexisting neutralizing antibodies were not protected from HPV16 E7-positive TC-1 tumor challenge, compared to the protection seen in mice lacking these antibodies. Antibody-coated VLPs bound very inefficiently to receptor-positive cell lines, suggesting that one of the mechanisms of antibody interference is blocking of VLP binding to its receptor and thereby uptake of VLPs by antigen-presenting cells. Our results suggest that repetitive vaccination with a cVLP for induction of cellular immune responses to an incorporated antigen may be of limited effectiveness due to the presence of neutralizing antibodies against the capsid proteins induced after the first application. This limitation could potentially be overcome by boosting with cVLPs containing the same target antigen incorporated into other papillomavirus-type VLPs.

摘要

携带人乳头瘤病毒16型(HPV16)E7蛋白的嵌合型人乳头瘤病毒样颗粒(HPV cVLPs)是在动物模型中诱导针对HPV诱导肿瘤的细胞介导免疫(CMI)的有效疫苗。我们检验了这样一个假设:初次接种疫苗期间产生的病毒体中和抗体可能会阻止CMI对cVLPs的有效增强。通过用野生型病毒样颗粒直接免疫或通过被动转移超免疫抗HPV16病毒样颗粒小鼠血清产生循环HPV16中和抗体的小鼠,随后用含HPV16 E7的cVLPs进行接种。与缺乏这些抗体的小鼠所表现出的保护作用相比,预先存在中和抗体的小鼠并未免受HPV16 E7阳性TC-1肿瘤的攻击。抗体包被的病毒样颗粒与受体阳性细胞系的结合效率非常低,这表明抗体干扰的机制之一是阻断病毒样颗粒与其受体的结合,从而阻止抗原呈递细胞摄取病毒样颗粒。我们的结果表明,由于首次接种后诱导产生了针对衣壳蛋白的中和抗体,用cVLP重复接种以诱导对掺入抗原的细胞免疫反应可能效果有限。通过用含有掺入其他乳头瘤病毒型病毒样颗粒中的相同靶抗原的cVLPs进行加强免疫,有可能克服这一限制。

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