Department of Preventive Medicine, Public Health and Microbiology, Universidad Autónoma, Madrid, Spain.
J Virol. 2014 May;88(10):5511-23. doi: 10.1128/JVI.00468-14. Epub 2014 Mar 5.
Due to the essential role macrophages play in antiviral immunity, it is important to understand the intracellular and molecular processes that occur in macrophages following infection with various strains of vaccinia virus, particularly those used as vaccine vectors. Similarities as well as differences were found in macrophages infected with different poxvirus strains, particularly at the level of virus-induced apoptosis and the expression of immunomodulatory genes, as determined by microarray analyses. Interestingly, the attenuated modified vaccinia Ankara virus (MVA) was particularly efficient in triggering apoptosis and beta interferon (IFN-β) secretion and in inducing changes in the expression of genes associated with increased activation of innate immunity, setting it apart from the other five vaccinia virus strains tested. Taken together, these results increase our understanding of how these viruses interact with human macrophages, at the cellular and molecular levels, and suggest mechanisms that may underlie their utility as recombinant vaccine vectors.
Our studies clearly demonstrate that there are substantial biological differences in the patterns of cellular gene expression between macrophages infected with different poxvirus strains and that these changes are due specifically to infection with the distinct viruses. For example, a clear induction in IFN-β mRNA was observed after infection with MVA but not with other poxviruses. Importantly, antiviral bioassays confirmed that MVA-infected macrophages secreted a high level of biologically active type I IFN. Similarly, the phagocytic capacity of macrophages was also specifically increased after infection with MVA. Although the main scope of this study was not to test the vaccine potential of MVA as there are several groups in the field working extensively on this aspect, the characteristics/phenotypes we observed at the in vitro level clearly highlight the inherent advantages that MVA possesses in comparison to other poxvirus strains.
由于巨噬细胞在抗病毒免疫中起着重要作用,因此了解巨噬细胞感染各种痘苗病毒(尤其是用作疫苗载体的那些病毒)后的细胞内和分子过程非常重要。通过微阵列分析发现,感染不同痘苗病毒株的巨噬细胞存在相似之处和差异,特别是在病毒诱导的细胞凋亡和免疫调节基因表达水平上。有趣的是,减毒的改良安卡拉牛痘病毒(MVA)在触发细胞凋亡和β干扰素(IFN-β)分泌以及诱导与固有免疫激活增加相关的基因表达变化方面非常有效,使其有别于测试的其他五种痘苗病毒株。总之,这些结果增加了我们对这些病毒如何在细胞和分子水平上与人巨噬细胞相互作用的理解,并提出了可能是它们作为重组疫苗载体的效用的基础的机制。
我们的研究清楚地表明,感染不同痘苗病毒株的巨噬细胞之间的细胞基因表达模式存在明显的生物学差异,并且这些变化是由特定的病毒感染引起的。例如,在用 MVA 感染后观察到 IFN-β mRNA 的明显诱导,但在用其他痘苗病毒感染后则没有。重要的是,抗病毒生物测定证实,MVA 感染的巨噬细胞分泌高水平的具有生物活性的 I 型 IFN。同样,在用 MVA 感染后,巨噬细胞的吞噬能力也特异性增加。尽管本研究的主要目的不是测试 MVA 的疫苗潜力,因为该领域有几个小组在这方面进行了广泛的研究,但我们在体外水平观察到的特征/表型清楚地突出了 MVA 与其他痘苗病毒株相比所具有的固有优势。