{"title":"The SCHOOL of nature: IV. Learning from viruses.","authors":"Alexander B Sigalov","doi":"10.4161/self.1.4.13279","DOIUrl":null,"url":null,"abstract":"<p><p>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 modulate signaling mediated by cell surface receptors. Despite tremendous advancement in recent years, the exact molecular mechanisms underlying these critical points in viral pathogenesis remain unknown. In this work, based on a novel platform of receptor signaling, the Signaling Chain HOmoOLigomerization (SCHOOL) platform, I suggest specific mechanisms used by different viruses such as human immunodeficiency virus (HIV), cytomegalovirus (CMV), severe acute respiratory syndrome coronavirus, human herpesvirus 6 and others, to modulate receptor signaling. I also use the example of HIV and CMV to illustrate how two unrelated enveloped viruses use a similar SCHOOL mechanism to modulate the host immune response mediated by two functionally different receptors: 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 non-viral pathogens. Learning from viruses how to target cell surface receptors not only helps us understand viral strategies to escape from the host immune surveillance, but also provides novel avenues in rational drug design and the development of new therapies for immune disorders.</p>","PeriodicalId":89270,"journal":{"name":"Self/nonself","volume":"1 4","pages":"282-298"},"PeriodicalIF":0.0000,"publicationDate":"2010-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062383/pdf/self0104_0282.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Self/nonself","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4161/self.1.4.13279","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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 modulate signaling mediated by cell surface receptors. Despite tremendous advancement in recent years, the exact molecular mechanisms underlying these critical points in viral pathogenesis remain unknown. In this work, based on a novel platform of receptor signaling, the Signaling Chain HOmoOLigomerization (SCHOOL) platform, I suggest specific mechanisms used by different viruses such as human immunodeficiency virus (HIV), cytomegalovirus (CMV), severe acute respiratory syndrome coronavirus, human herpesvirus 6 and others, to modulate receptor signaling. I also use the example of HIV and CMV to illustrate how two unrelated enveloped viruses use a similar SCHOOL mechanism to modulate the host immune response mediated by two functionally different receptors: 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 non-viral pathogens. Learning from viruses how to target cell surface receptors not only helps us understand viral strategies to escape from the host immune surveillance, but also provides novel avenues in rational drug design and the development of new therapies for immune disorders.
在病毒与宿主共同进化的过程中,宿主为自己配备了复杂的免疫系统,以抵御病毒的入侵。为了在宿主体内成功感染、复制和存活,病毒进化出了许多策略来对抗和躲避宿主的抗病毒免疫反应,并利用这些反应进行富有成效的病毒复制。这些策略包括调节由细胞表面受体介导的信号传导。尽管近年来取得了巨大进步,但病毒致病过程中这些关键点的确切分子机制仍然未知。在这项研究中,我基于一个新颖的受体信号平台--信号链HOmoOLigomerization(SCHOOL)平台,提出了人类免疫缺陷病毒(HIV)、巨细胞病毒(CMV)、严重急性呼吸系统综合征冠状病毒、人类疱疹病毒6等不同病毒用于调节受体信号的具体机制。我还以艾滋病毒和巨细胞病毒为例,说明两种不相关的包膜病毒是如何利用类似的 SCHOOL 机制来调节由两种功能不同的受体介导的宿主免疫反应的:T细胞抗原受体和自然杀伤细胞受体NKp30。这表明,其他病毒病原体和可能的非病毒病原体也可能或正在使用类似的一般机制。从病毒身上学习如何以细胞表面受体为靶标,不仅有助于我们了解病毒逃避宿主免疫监视的策略,还为合理的药物设计和免疫疾病新疗法的开发提供了新的途径。