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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >The co-speciation of human cytomegalovirus (HCMV) with its human host has enabled this human pathogen to evolve multiple mechanisms to allow it to be carried, generally sub-clinically, for the lifetime of the host in the face of a robust immune response. Preface.
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The co-speciation of human cytomegalovirus (HCMV) with its human host has enabled this human pathogen to evolve multiple mechanisms to allow it to be carried, generally sub-clinically, for the lifetime of the host in the face of a robust immune response. Preface.

机译:人类巨细胞病毒的co-speciation()血巨细胞病毒人类宿主使人类多个机制,使病原体的进化进行,一般肿瘤,主人的生命,面对一个健壮的免疫反应。

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The co-speciation of human cytomegalovirus (HCMV) with its human host has enabled this human pathogen to evolve multiple mechanisms to allow it to be carried, generally sub-clinically, for the lifetime of the host in the face of a robust immune response. This life-long carriage is maintained by low-level persistence as well as by latent infection and involves host/virus interactions which are necessarily diverse and complex. These interactions ensure conditions whereby virus is able to maximise viral carriage and dissemination whilst avoiding immunesurveillance. It must be said that, in the case of HCMV, this generally results in an innocuous balance between the host and the virus unless the balance is upset by, for instance, disruption of host immunity.
机译:人类巨细胞病毒的co-speciation()血巨细胞病毒人类宿主使人类多个机制,使病原体的进化进行,一般肿瘤,主人的生命,面对一个健壮的免疫反应。由低级的持久性以及维护潜伏性感染,包括主机/病毒必然是多元化和相互作用复杂。,病毒能够最大化病毒马车和传播而避免immunesurveillance。血巨细胞病毒案例,这通常导致一个无伤大雅的宿主和病毒之间的平衡例如,除非这种平衡被打破了破坏宿主免疫力。

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