Recombinant Chimeric Virus-like Particles of Human Papillomavirus Produced by Distinct Cell Lineages: Potential as Prophylactic Nanovaccine and Therapeutic Drug Nanocarriers.

IF 3.5 3区 医学 Q2 VIROLOGY
Viruses-Basel Pub Date : 2025-09-04 DOI:10.3390/v17091209
Cyntia Silva Oliveira, Dirce Sakauchi, Érica Akemi Kavati Sasaki, Aurora Marques Cianciarullo
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引用次数: 0

Abstract

Antigenicity and immunogenicity define a potent immunogen in vaccinology. Nowadays, there are simplified platforms to produce nanocarriers for small-peptide antigen delivery, derived from various infectious agents for the treatment of a variety of diseases, based on virus-like particles (VLPs). They have good cell-penetrating properties and protective action for target molecules from degradation. Human papillomavirus (HPV) causes anogenital warts and six types of cancer in infected women, men, or children, posing a challenge to global public health. The HPV capsid is composed of viral type-specific L1 and evolutionarily conserved L2 proteins. Produced in heterologous systems, the L1 protein can self-assemble into VLPs, nanoparticles sized around 50-60 nm, used as prophylactic vaccines. Devoid of the viral genome, they are safe for users, offering no risk of infection because VLPs do not replicate. The immune response induced by HPV VLPs is promoted by conformational viral epitopes, generating effective T- and B-cell responses. Produced in different cell systems, HPV16 L1 VLPs can be obtained on a large scale for use in mass immunization programs, which are well established nowadays. The expression of heterologous proteins was evaluated at various transfection times by transfecting cells with vectors encoding codon-optimized HPV16L1 and HPV16L2 genes. Immunological response induced by chimeric HPV16 L1/L2 VLP was evaluated through preclinical assays by antibody production, suggesting the potential of broad-spectrum protection against HPV as a prophylactic nanovaccine. These platforms can also offer promising therapeutic strategies, covering the various possibilities for complementary studies to develop potential preventive and therapeutic vaccines with broad-spectrum protection, using in silico new epitope selection and innovative nanotechnologies to obtain more effective immunobiologicals in combating HPV-associated cancers, influenza, hepatitis B and C, tuberculosis, human immunodeficiency virus (HIV), and many other illnesses.

不同细胞系产生的人乳头瘤病毒重组嵌合病毒样颗粒:作为预防性纳米疫苗和治疗性药物纳米载体的潜力
抗原原性和免疫原性在疫苗学中定义了一种有效的免疫原。如今,基于病毒样颗粒(vlp),有简化的平台来生产用于小肽抗原递送的纳米载体,这些纳米载体来自于治疗各种疾病的各种感染因子。它们具有良好的细胞穿透性能和对靶分子降解的保护作用。人乳头瘤病毒(HPV)在受感染的女性、男性或儿童中引起肛门生殖器疣和六种癌症,对全球公共卫生构成挑战。HPV衣壳由病毒类型特异性L1和进化保守的L2蛋白组成。在异源系统中产生的L1蛋白可以自组装成vlp,一种大小约为50-60纳米的纳米颗粒,用于预防性疫苗。由于没有病毒基因组,它们对使用者来说是安全的,没有感染的风险,因为vlp不会复制。由HPV VLPs诱导的免疫应答由构象病毒表位促进,产生有效的T细胞和b细胞应答。在不同的细胞系统中产生,HPV16 L1 VLPs可以大规模获得,用于目前已建立的大规模免疫规划。通过编码密码子优化的HPV16L1和HPV16L2基因的载体转染细胞,在不同的转染时间评估异种蛋白的表达。嵌合HPV16 L1/L2 VLP诱导的免疫应答通过抗体生产的临床前试验进行评估,表明作为预防性纳米疫苗具有广谱保护HPV的潜力。这些平台还可以提供有希望的治疗策略,涵盖各种可能性进行补充性研究,以开发具有广谱保护的潜在预防性和治疗性疫苗,在计算机上使用新的表位选择和创新纳米技术,以获得更有效的免疫生物制剂,以对抗hpv相关的癌症、流感、乙型和丙型肝炎、结核病、人类免疫缺陷病毒(艾滋病毒)和许多其他疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Viruses-Basel
Viruses-Basel VIROLOGY-
CiteScore
7.30
自引率
12.80%
发文量
2445
审稿时长
1 months
期刊介绍: Viruses (ISSN 1999-4915) is an open access journal which provides an advanced forum for studies of viruses. It publishes reviews, regular research papers, communications, conference reports and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. We also encourage the publication of timely reviews and commentaries on topics of interest to the virology community and feature highlights from the virology literature in the ''News and Views'' section. Electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
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