Poxvirus and Rabies Branch, Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30329, USA; Chronic Viral Diseases Branch, Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30329, USA.
Poxvirus and Rabies Branch, Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30329, USA.
Virus Res. 2018 Mar 15;248:39-43. doi: 10.1016/j.virusres.2018.02.012. Epub 2018 Feb 19.
This study investigates the production of rabies virus (RABV) neutralizing antibody after virus infection through a mouse model. The BALB/c mice from different age groups (three, five, seven week old) were intramuscularly inoculated with live rabies virus (TX coyote 323R). Without pre-exposure or post-exposure prophylaxis (PEP), we found there is a decreased fatality with increased age of animals, the mortalities are 60%, 50%, and 30%, respectively. Interestingly, through assay of rapid fluorescent focus inhibition test (RFFIT), direct fluorescent antibody (DFA) and quantitative Polymerase Chain Reaction (qPCR), the results showed that all the animals that succumbed to rabies challenge, except one, developed circulating neutralizing antibodies, and all the healthy animals, except two, did not generate virus neutralizing antibodies (VNA). Our animal study suggests that the induction of VNA was an indicator of infection progression in the central nervous system (CNS) and speculate that RABV neutralizing antibodies did not cross the blood-brain barrier of the CNS for those diseased animals. We hypothesize that early release of viral antigens from damaged nerve tissue might potentially be a benefit for survivors, and we also discuss several other aspects of the interaction of RABV and its neutralizing antibodies.
本研究通过小鼠模型探究了病毒感染后狂犬病毒(RABV)中和抗体的产生。将来自不同年龄组(3、5、7 周龄)的 BALB/c 小鼠通过肌肉内接种活狂犬病毒(TX 郊狼 323R)。未经预先暴露或暴露后预防(PEP),我们发现动物的年龄越大,死亡率越低,分别为 60%、50%和 30%。有趣的是,通过快速荧光灶抑制试验(RFFIT)、直接荧光抗体(DFA)和定量聚合酶链反应(qPCR)检测,结果表明,除 1 只外,所有死于狂犬病挑战的动物均产生了循环中和抗体,除 2 只外,所有健康动物均未产生病毒中和抗体(VNA)。我们的动物研究表明,VNA 的诱导是中枢神经系统(CNS)感染进展的一个指标,并推测 RABV 中和抗体没有穿过 CNS 的血脑屏障。我们假设受损神经组织中病毒抗原的早期释放可能对幸存者有益,我们还讨论了 RABV 及其中和抗体相互作用的几个其他方面。