Jackson Ronald J, Boyle David B, Ranasinghe Charani
Molecular Mucosal Vaccine Immunology group, Department of Immunology, The John Curtin School of Medical Research, The Australian National University, Canberra, ACT, 2601, Australia.
Methods Mol Biol. 2014;1143:61-90. doi: 10.1007/978-1-4939-0410-5_5.
Although recombinant DNA and recombinant viral vectors expressing HIV antigens have yielded positive outcomes in animal models, these vaccines have not been effectively translated to humans. Despite this, there is still a high level of optimism that poxviral-based vaccine strategies could offer the best hope for developing an effective vaccine against not only HIV-1 but also other chronic diseases where good-quality T and B cell immunity is needed for protection. In this chapter we discuss step by step (1) how recombinant poxviral vectors co-expressing HIV antigens and promising mucosal/systemic adjuvants (e.g., IL-13Rα2) are constructed, (2) how these vectors can be used in alternative heterologous prime-boost immunization strategies, (3) how systemic and mucosal samples are prepared for analysis, followed by (4) two immunological assays: multicolor intracellular cytokine staining and tetramer/homing maker analysis that are used to evaluate effective systemic and mucosal T cell immunity.
尽管表达HIV抗原的重组DNA和重组病毒载体在动物模型中已产生了积极成果,但这些疫苗尚未有效地转化应用于人类。尽管如此,人们仍然高度乐观地认为,基于痘病毒的疫苗策略不仅有望开发出针对HIV-1的有效疫苗,还能为其他需要高质量T细胞和B细胞免疫来提供保护的慢性疾病带来最大希望。在本章中,我们将逐步讨论:(1)如何构建共表达HIV抗原和有前景的黏膜/全身佐剂(如IL-13Rα2)的重组痘病毒载体;(2)如何将这些载体用于替代性异源初免-加强免疫策略;(3)如何制备用于分析的全身和黏膜样本;随后是(4)两种免疫学检测方法:多色细胞内细胞因子染色和四聚体/归巢标志物分析,用于评估有效的全身和黏膜T细胞免疫。