School of Molecular and Biomedical Science, University of Adelaide , Adelaide, South Australia, Australia ; SA Pathology , Adelaide, South Australia, Australia.
School of Molecular and Biomedical Science, University of Adelaide , Adelaide, South Australia, Australia.
Clin Transl Immunology. 2014 Sep 26;3(9):e24. doi: 10.1038/cti.2014.22. eCollection 2014 Sep.
Broadly neutralizing antibodies (bNAbs) are a consistent protective immune correlate in human immunodeficiency virus (HIV) patients as well as in passive immunotherapy studies. The inability to elicit bNAbs is the core reason underlining the repeated failures in traditional HIV vaccine research. Rare monoclonal bNAbs against HIV, however, have been produced. The significance of producing and studying more monoclonal bNAbs against HIV is underlined by its capability of defining critical epitopes for antigen designs aimed at the development of a serum-neutralizing HIV vaccine. In this regard, traditional antigen preparations have failed. There is a need to clearly advocate the concept, and systematic study, of more sophisticated 'designer antigens' (DAGs), which carry epitopes that can lead to the elicitation of bNAbs. Using an extremely efficient cell-to-cell HIV infection model for the preparation of HIV prefusion intermediates, we have investigated a novel and systematic approach to produce (not screen for) potential bNAbs against HIV. We have established the concept and the experimental system for producing formaldehyde-fixed HIV DAGs that carry temperature-arrested prefusion intermediates. These prefusion intermediates are structures on the cell surface after viral attachment and receptor engagement but before fully functional viral entry. Using defined HIV prefusion DAGs, we have produced monoclonal antibodies (mAbs) specific to novel epitopes on HIV prefusion intermediates. These mAbs do not react with the static/native surface HIV or cellular antigens, but react with the DAGs. This is a paradigm shift from the current mainstream approach of screening elite patients' bNAbs.
广谱中和抗体(bNAbs)是人类免疫缺陷病毒(HIV)患者以及被动免疫治疗研究中的一致保护性免疫相关物。不能诱导 bNAbs 是传统 HIV 疫苗研究反复失败的核心原因。然而,已经产生了针对 HIV 的稀有单克隆 bNAbs。产生和研究更多针对 HIV 的单克隆 bNAbs 的重要性在于其能够定义针对开发血清中和 HIV 疫苗的抗原设计的关键表位。在这方面,传统的抗原制剂已经失败。需要明确提倡更复杂的“设计抗原”(DAG)的概念和系统研究,这些抗原带有可以诱导 bNAbs 的表位。我们使用一种极其有效的细胞间 HIV 感染模型来制备 HIV 融合前中间体,以研究一种新的、系统的方法来产生(而不是筛选)针对 HIV 的潜在 bNAbs。我们已经建立了概念和实验系统,用于生产携带温度捕获融合前中间体的甲醛固定 HIV DAG。这些融合前中间体是病毒附着和受体结合后但在完全功能性病毒进入之前在细胞表面上的结构。使用定义的 HIV 融合前 DAG,我们产生了针对 HIV 融合前中间体上新型表位的单克隆抗体(mAbs)。这些 mAbs 与静态/天然表面 HIV 或细胞抗原不反应,但与 DAG 反应。这是从当前筛选精英患者 bNAbs 的主流方法的范式转变。