mhc - i限制性HIV表位加工、免疫控制和免疫原设计

HIV therapy Pub Date : 2010-01-01 DOI:10.2217/HIV.09.57
S. Gall
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引用次数: 2

摘要

在发现艾滋病毒超过25年后,尽管进行了几次疫苗试验,但免疫保护的相关因素仍未确定。成功的疫苗战略可能涉及诱导体液和细胞免疫,以预防或限制艾滋病毒感染并刺激艾滋病毒感染者的保护性免疫反应。这一探索的主要困难包括艾滋病毒产生的各种免疫逃逸机制,以及并非所有针对艾滋病毒的免疫反应都具有强大的抗病毒功能。这篇文章将聚焦于任何基于t细胞的疫苗策略的一个被低估的方面:表位加工的机制及其对hiv特异性CD8+ t细胞应答模式的贡献。本文还将介绍目前CD8+ t细胞保护性免疫反应的鉴定和免疫原的设计,这些免疫原旨在选择性地诱导CD8+ t细胞对HIV、HIV和HIV的保护性免疫反应。
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MHC-I-restricted HIV epitope processing, immune control and immunogen design
More than 25 years after the discovery of HIV and despite several vaccine trials, the correlates of immune protection are still not identified. Successful vaccine strategies will likely involve induction of both humoral and cellular immunity in order to prevent or limit HIV infection and to stimulate protective immune responses in HIV-infected individuals. The major difficulties in this quest include the various mechanisms of immune escape developed by HIV and the fact that not all immune responses against HIV have strong antiviral functions. This article will focus on an underestimated aspect of any T-cell-based arm of vaccine strategies: the mechanisms of epitope processing and its contribution to the pattern of HIV-specific CD8+ T-cell responses. This article will also present current complementary research approaches towards the identification of CD8+ T-cell protective immune responses and the design of immunogens aimed at selectively inducing CD8+ T-cell protective immune responses against HIV, one o...
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