Patterson Steven, Papagatsias Timos, Benlahrech Adel
Department of Immunology, Imperial College, Chelsea and Westminster Hospital, London, UK.
Handb Exp Pharmacol. 2009(188):275-93. doi: 10.1007/978-3-540-71029-5_13.
The best hope of controlling the HIV pandemic is the development of an effective vaccine. In addition to the stimulation of virus neutralising antibodies, a vaccine will need an effective T-cell response against the virus. Vaccines based on recombinant adenoviruses (rAd) are promising candidates to stimulate anti-HIV T-cell responses. This review discusses the different rAd vector types, problems raised by host immune responses against them and strategies that are being adopted to overcome this problem. Vaccines need to target and stimulate dendritic cells and thus the tropism and interaction of rAd-based vaccines with these cells is covered. Different rAd vaccination regimes and the need to stimulate mucosal responses are discussed together with data from animal studies on immunogenicity and virus challenge experiments. The review ends with a discussion of the recent disappointing Merck HIV vaccine trial.
控制艾滋病大流行的最大希望在于研发出一种有效的疫苗。除了刺激病毒中和抗体外,疫苗还需要对病毒产生有效的T细胞应答。基于重组腺病毒(rAd)的疫苗是刺激抗HIV T细胞应答的有前景的候选疫苗。本文综述讨论了不同类型的rAd载体、宿主针对它们的免疫反应所引发的问题以及为克服这一问题而采用的策略。疫苗需要靶向并刺激树突状细胞,因此本文涵盖了基于rAd的疫苗与这些细胞的嗜性和相互作用。文中讨论了不同的rAd疫苗接种方案以及刺激黏膜反应的必要性,并结合了动物免疫原性研究和病毒攻击实验的数据。本文最后讨论了默克公司近期令人失望的HIV疫苗试验。