Münz Christian
Viral Immunobiology, Institute of Experimental Immunology, University of Zürich, Switzerland.
Immunol Lett. 2014 Sep;161(1):118-24. doi: 10.1016/j.imlet.2014.05.012. Epub 2014 Jun 2.
Pathogenic viruses are often difficult to study due to their exclusive tropism for humans. The development of mice with human immune system components opens the possibility to study those human pathogens with a tropism for the human hematopoietic lineage in vivo. These include HCMV, EBV, KSHV, HIV, HTLV-1, dengue virus and JC virus. Furthermore, some human pathogens, like HSV-2, adenovirus, HCV, HBV and influenza A virus, with an additional tropism for somatic mouse tissues or for additional transplanted human tissues, mainly liver, have been explored in these models. The cellular tropism of these viruses, their associated diseases and primarily cell-mediated immune responses to these viral infections will be discussed in this review. Already some exciting information has been gained from these novel chimeric in vivo models and future avenues to gain more insights into the pathology, but also potential therapies, will be outlined. Although the respective in vivo models of human immune responses can still be significantly improved, they already provide preclinical systems for in vivo studies of important viral pathogens of humans.
由于致病病毒对人类具有独特的嗜性,它们往往难以研究。具有人类免疫系统成分的小鼠的开发为在体内研究那些对人类造血谱系具有嗜性的人类病原体提供了可能性。这些病原体包括人巨细胞病毒(HCMV)、爱泼斯坦-巴尔病毒(EBV)、卡波西肉瘤相关疱疹病毒(KSHV)、人类免疫缺陷病毒(HIV)、人类嗜T淋巴细胞病毒1型(HTLV-1)、登革病毒和JC病毒。此外,一些对小鼠体细胞组织或对其他移植的人类组织(主要是肝脏)具有额外嗜性的人类病原体,如单纯疱疹病毒2型(HSV-2)、腺病毒、丙型肝炎病毒(HCV)、乙型肝炎病毒(HBV)和甲型流感病毒,已在这些模型中得到研究。本文将讨论这些病毒的细胞嗜性、它们相关的疾病以及对这些病毒感染主要的细胞介导免疫反应。已经从这些新型嵌合体内模型中获得了一些令人兴奋的信息,并且将概述未来获得更多病理学见解以及潜在治疗方法的途径。尽管人类免疫反应的各自体内模型仍有显著改进的空间,但它们已经为人类重要病毒病原体的体内研究提供了临床前系统。