Irsicaixa - AIDS Research Institute, Badalona.
Universitat de Vic-Universitat Central de Catalunya (UVic-UCC), Vic.
Curr Opin HIV AIDS. 2022 Nov 1;17(6):333-337. doi: 10.1097/COH.0000000000000765. Epub 2022 Sep 19.
Not all T-cell responses against HIV are created equally and responses of certain epitope specificities have been associated with superior control of infection. These insights have spurred the development of a wide range of immunogen sequences, each with particular advantages and limitations.
We review some of the most advanced designs that have reached or are close to reaching human clinical trials, with a special focus on T-cell immunogen developed for therapeutic use. We also touch upon the importance of how immunogens are delivered and point out the lamentable fact that there is essentially no alignment between different designs and vaccine regimens, which is a major hindrance to accelerated advances in the field.
The design of an immunogen able to induce T-cell responses of adequate specificity and functionality is subject of a wide range of preclinical and clinical studies. Few designs have shown promise to date, but emerging data highlight the critical contribution of specificity to effective antiviral activity in vivo .
并非所有针对 HIV 的 T 细胞反应都是平等产生的,某些表位特异性的反应与更好地控制感染有关。这些见解促使人们开发了广泛的免疫原序列,每种序列都有其特定的优点和局限性。
我们回顾了一些已经进入或接近人体临床试验的最先进的设计,特别关注为治疗用途开发的 T 细胞免疫原。我们还谈到了免疫原传递的重要性,并指出一个可悲的事实,即不同的设计和疫苗方案之间基本上没有一致性,这是该领域加速进展的主要障碍。
能够诱导具有足够特异性和功能的 T 细胞反应的免疫原的设计是广泛的临床前和临床研究的主题。迄今为止,少数设计显示出了希望,但新出现的数据强调了特异性对体内有效抗病毒活性的关键贡献。