Virology Unit, Department of Biomedical Sciences, Institute of Tropical Medicine of Antwerp, Nationalestraat 155, B-2000, Antwerpen, Belgium.
Retrovirology. 2012 Sep 7;9:72. doi: 10.1186/1742-4690-9-72.
Immunotherapy aims to assist the natural immune system in achieving control over viral infection. Various immunotherapy formats have been evaluated in either therapy-naive or therapy-experienced HIV-infected patients over the last 20 years. These formats included non-antigen specific strategies such as cytokines that stimulate immunity or suppress the viral replication, as well as antibodies that block negative regulatory pathways. A number of HIV-specific therapeutic vaccinations have also been proposed, using in vivo injection of inactivated virus, plasmid DNA encoding HIV antigens, or recombinant viral vectors containing HIV genes. A specific format of therapeutic vaccines consists of ex vivo loading of autologous dendritic cells with one of the above mentioned antigenic formats or mRNA encoding HIV antigens.This review provides an extensive overview of the background and rationale of these different therapeutic attempts and discusses the results of trials in the SIV macaque model and in patients. To date success has been limited, which could be explained by insufficient quality or strength of the induced immune responses, incomplete coverage of HIV variability and/or inappropriate immune activation, with ensuing increased susceptibility of target cells.Future attempts at therapeutic vaccination should ideally be performed under the protection of highly active antiretroviral drugs in patients with a recovered immune system. Risks for immune escape should be limited by a better coverage of the HIV variability, using either conserved or mosaic sequences. Appropriate molecular adjuvants should be included to enhance the quality and strength of the responses, without inducing inappropriate immune activation. Finally, to achieve a long-lasting effect on viral control (i.e. a "functional cure") it is likely that these immune interventions should be combined with anti-latency drugs and/or gene therapy.
免疫疗法旨在帮助人体自然免疫系统控制病毒感染。在过去的 20 年中,针对未经治疗或已治疗的 HIV 感染者,已经评估了多种免疫疗法。这些方法包括非抗原特异性策略,如刺激免疫或抑制病毒复制的细胞因子,以及阻断负调节途径的抗体。还提出了许多 HIV 特异性治疗性疫苗,包括体内注射灭活病毒、编码 HIV 抗原的质粒 DNA 或含有 HIV 基因的重组病毒载体。一种特定形式的治疗性疫苗包括用上述抗原形式之一或编码 HIV 抗原的 mRNA 对自体树突状细胞进行体外加载。本综述广泛概述了这些不同治疗尝试的背景和原理,并讨论了 SIV 猕猴模型和患者试验的结果。迄今为止,成功有限,这可以用诱导的免疫反应质量或强度不足、HIV 变异性不完全覆盖和/或免疫激活不当来解释,从而导致靶细胞易感性增加。在免疫系统恢复的患者中,在高效抗逆转录病毒药物的保护下,治疗性疫苗的未来尝试应理想地进行。通过使用保守或镶嵌序列,风险应通过更好地覆盖 HIV 变异性来限制免疫逃逸。应包含适当的分子佐剂,以增强反应的质量和强度,而不会引起不当的免疫激活。最后,为了实现对病毒控制的持久影响(即“功能性治愈”),这些免疫干预可能需要与抗潜伏药物和/或基因治疗相结合。