[利用动物模型阐明病毒-宿主相互作用用于疫苗开发]。

Uirusu Pub Date : 2025-01-01 DOI:10.2222/jsv.75.51
Hiroshi Ishii
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引用次数: 0

摘要

HIV复制与宿主免疫高度相互作用,在适应性免疫反应的存在下导致终生持续的病毒复制。开发有效的疫苗是控制全球艾滋病毒流行的关键,但诱导有效的抗艾滋病毒免疫反应的免疫方法尚未建立。我们一直专注于利用动物模型分析病毒-宿主免疫相互作用,并将研究结果应用于疫苗的开发。我们开发了一种新的免疫原,选择性地诱导病毒特异性CD8+ t细胞反应,并显示出疫苗对直肠内SIV攻击的保护作用。我们还研究了抗体反应,并确定了猕猴种系免疫球蛋白基因的多态性及其与诱导一类特定的抗siv中和抗体的关系。我们将HIV研究的知识应用于HTLV和COVID-19,在猕猴模型中显示了疫苗诱导的HTLV中和抗体对HTLV感染的保护作用以及疫苗诱导的CD8+ t细胞对SARS-CoV-2的病毒抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Elucidation of virus-host interaction using animal models towards vaccine development].

HIV replication highly interacts with host immunity resulting in life-long persistent virus replication in the presence of adaptive immune responses. Development of an effective vaccine is a key for control of global HIV epidemic, but immunization methods to induce effective anti-HIV immune responses have not been established. We have been focusing on analyzing virus-host immune interaction in vivo using animal models and applying findings to the development of vaccines. We have developed a novel immunogen selectively inducing virus-specific CD8+ T-cell responses and showed protective efficacy of vaccines against intrarectal SIV challenge. We have also worked on antibody responses, and determined the polymorphism in germline immunoglobulin genes in macaques and its association with induction of a particular class of anti-SIV neutralizing antibody. We applied the knowledge in HIV research to HTLV and COVID-19, showing protective efficacy of vaccine-induced neutralizing antibody against HTLV infection and viral suppression by vaccine-induced CD8+ T-cell responses against SARS-CoV-2 in macaque models.

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