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Anti-coxsackievirus B4 (CV-B4) enhancing activity of serum associated with increased viral load and pathology in mice reinfected with CV-B4

机译:抗柯萨奇病毒B4(CV-B4)在重新感染CV-B4的小鼠中增强血清活性并与病毒载量和病理变化有关

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ABSTRACT In previous studies it was shown that inoculation of Swiss albino mice with CV-B4 E2 resulted in the production of serum IgG capable of enhancing the CV-B4 E2 infection of murine spleen cells cultures. To investigate whether such an enhancing activity of serum can play a role in vivo, we decided to study the CV-B4 E2 infection in mice exposed to successive inoculations of virus. In Swiss albino mice infected with CV-B4 E2 at the age of 21?days, anti-CV-B4 E2 neutralizing and enhancing activities of their serum peaked after 55 d. In contrast, mice inoculated at the age of 55 d expressed much lower activities. Despite the neutralizing activity of serum, CV-B4 E2 inoculated a second time to 55?day-old animals spread into the host. At the age of 72 and 89 d the levels of viral RNA and infectious particles were higher in organs of animals exposed to 2 successive infections compared with animals infected once at the age of 21 d or 55 d. In animals with 2 successive inoculations of CV-B4 E2 there was a relationship between the anti-CV-B4 E2 enhancing activity of serum and the level of viral RNA in organs and an enhancement of pathology was observed as displayed by histological analysis of pancreas and hyperglycaemia. Altogether our data strongly suggest that an anti-CV-B4 E2 enhancing activity in the host can play a role in the outcome of a secondary infection with this virus.
机译:摘要在以前的研究中,发现用CV-B4 E2接种瑞士白化病小鼠会导致血清IgG的产生,该血清IgG可以增强鼠脾细胞培养物中CV-B4 E2的感染。为了研究血清的这种增强活性是否可以在体内发挥作用,我们决定在暴露于连续疫苗的小鼠中研究CV-B4 E2感染。在21天的CV-B4 E2感染的瑞士白化病小鼠中,抗CV-B4 E2的中和和增强血清活性在55天后达到峰值。相反,在55 d龄接种的小鼠表达的活性要低得多。尽管有血清中和活性,CV-B4 E2还是第二次接种到了55日龄的动物身上。与分别在21 d或55 d感染一次的动物相比,在两次连续感染的动物的器官中,72和89 d的病毒RNA和感染性颗粒的水平更高。在连续两次接种CV-B4 E2的动物中,血清抗CV-B4 E2的增强活性与器官中病毒RNA的水平之间存在相关性,并且通过对胰腺和肝脏的组织学分析显示,病理学得到了增强。高血糖症。总体而言,我们的数据强烈表明,宿主体内抗CV-B4 E2的增强活性可在该病毒的继发感染中发挥作用。

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