Kim Walter M, Sigalov Alexander B
Department of Pathology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA.
Adv Exp Med Biol. 2008;640:325-49. doi: 10.1007/978-0-387-09789-3_22.
During the co-evolution of viruses and their hosts, the latter have equipped themselves with an elaborate immune system to defend themselves from the invading viruses. In order to establish a successful infection, replicate and persist in the host, viruses have evolved numerous strategies to counter and evade host antiviral immune responses as well as exploit them for productive viral replication. These strategies include those that target immune receptor transmembrane signaling. Uncovering the exact molecular mechanisms underlying these critical points in viral pathogenesis will not only help us understand strategies used by viruses to escape from the host immune surveillance but also reveal new therapeutic targets for antiviral as well as immunomodulatory therapy. In this chapter, based on our current understanding of transmembrane signal transduction mediated by multichain immune recognition receptors (MIRRs) and the results of sequence analysis, we discuss the MIRR-targetingviral strategies of immune evasion and suggest their possible mechanisms that, in turn, reveal new points of antiviral intervention. We also show how two unrelated enveloped viruses, human immunodeficiency virus and human cytomegalovirus, use a similar mechanism to modulate the host immune response mediated by two functionally different MIRRs-T-cell antigen receptor and natural killer cell receptor, NKp30. This suggests that it is very likely that similar general mechanisms can be or are used by other viral and possibly nonviral pathogens.
在病毒与其宿主的共同进化过程中,宿主构建了一套复杂的免疫系统来抵御入侵的病毒。为了在宿主体内成功感染、复制并持续存在,病毒进化出了多种策略来对抗和逃避宿主的抗病毒免疫反应,同时利用这些反应进行有效的病毒复制。这些策略包括针对免疫受体跨膜信号传导的策略。揭示病毒发病机制中这些关键点背后的确切分子机制,不仅有助于我们理解病毒逃避宿主免疫监视所采用的策略,还能揭示抗病毒及免疫调节治疗的新靶点。在本章中,基于我们目前对多链免疫识别受体(MIRRs)介导的跨膜信号转导的理解以及序列分析结果,我们讨论了病毒针对MIRRs的免疫逃逸策略,并提出其可能的机制,这些机制反过来揭示了抗病毒干预的新靶点。我们还展示了两种不相关的包膜病毒,即人类免疫缺陷病毒和人类巨细胞病毒,如何利用相似的机制调节由两种功能不同的MIRRs——T细胞抗原受体和自然杀伤细胞受体NKp30介导的宿主免疫反应。这表明其他病毒以及可能的非病毒病原体很可能能够或正在使用类似的通用机制。