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一种基于人乳头瘤病毒16型和18型癌蛋白E6和E7的新型治疗性多表位疫苗:一种方法。

A novel therapeutic multiepitope vaccine based on oncoprotein E6 and E7 of HPV 16 and 18: An approach.

作者信息

Pratiwi Sari Eka, Ysrafil Ysrafil, Mardhia Mardhia, Mahyarudin Mahyarudin, Ilmiawan Muhammad Inam, Trianto Heru Fajar, Liana Delima Fajar, Amia Yuri

机构信息

Department of Biology and Pathobiology, Faculty of Medicine, Universitas Tanjungpura, ‎Pontianak, Indonesia.

Department of Pharmacology, Faculty of Medicine, Universitas Palangka Raya, Palangka ‎Raya, Indonesia.

出版信息

Bioimpacts. 2024;14(5):27846. doi: 10.34172/bi.2024.27846. Epub 2024 Feb 6.

Abstract

INTRODUCTION

The current vaccine strategies to prevent cervical cancer are effective only for individuals unexposed to HPV, lacking therapeutic effects against pre-existing infections. Multiepitope vaccines, using an immunoinformatic approach, are promising against tumors and viral infections because of their high specificity, safety, and stability, as well as the cheap cost of development.

METHODS

This study employed computer-based immunoinformatic analysis to design therapeutic multiepitope vaccines against cervical cancer using oncoproteins E6 and E7 of HPV 16 and 18. Several immunoinformatic tools were applied to analyze potential vaccine constructs capable of stimulating immune responses against both oncoproteins.

RESULTS

The constructed vaccine exhibited antigenic, immunogenic, nonallergenic, nontoxic, stable, and soluble characteristics. Additionally, it effectively interacted with TLR2 and TLR4, showing high binding capacity. Computational analysis indicated the vaccine could induce immune responses through the elevation of cytokine levels after the third injection, antibody production, activation of memory B and T cells, and promotion of increased dendritic cell counts.

CONCLUSION

The novel multiepitope vaccine based on E6 and E7 presented as a promising candidate for combating HPV infections and associated cervical cancer. Further and studies were essential to validate the efficacy and safety of the vaccine.

摘要

引言

目前预防宫颈癌的疫苗策略仅对未感染人乳头瘤病毒(HPV)的个体有效,对已存在的感染缺乏治疗效果。多表位疫苗采用免疫信息学方法,因其具有高特异性、安全性和稳定性,以及开发成本低廉,在对抗肿瘤和病毒感染方面具有广阔前景。

方法

本研究采用基于计算机的免疫信息学分析方法,利用HPV 16和18的癌蛋白E6和E7设计针对宫颈癌的治疗性多表位疫苗。应用多种免疫信息学工具分析能够刺激针对这两种癌蛋白的免疫反应的潜在疫苗构建体。

结果

构建的疫苗具有抗原性、免疫原性、无致敏性、无毒性、稳定性和可溶性等特性。此外,它能与Toll样受体2(TLR2)和Toll样受体4(TLR4)有效相互作用,显示出高结合能力。计算分析表明,该疫苗在第三次注射后可通过提高细胞因子水平、产生抗体、激活记忆B细胞和T细胞以及促进树突状细胞数量增加来诱导免疫反应。

结论

基于E6和E7的新型多表位疫苗有望成为对抗HPV感染及相关宫颈癌的候选疫苗。进一步的研究对于验证该疫苗的有效性和安全性至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf55/11406424/e95133c0165e/bi-14-27846-g001.jpg

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