Key result
Passive immunization with hyperimmune sera before or after EV71 infection in mice significantly reduced brainstem viral titers, delayed disease onset, and reduced disease severity and mortality.
Why the study?
Does passive immunization with hyperimmune sera reduce brainstem infection and mortality in a mouse model of Enterovirus 71?
Does passive immunization with hyperimmune sera reduce brainstem infection and mortality in a mouse model of Enterovirus 71?
Passive immunization with hyperimmune sera can ameliorate EV71 brainstem infection and reduce mortality in a mouse model, suggesting potential therapeutic benefit for patients with neurologic complications.
Should not yet change EV71 practice; hypothesis-generating for passive immunization in neurologic disease.
Enterovirus 71 (EV71)-associated hand, foot, and mouth disease may be complicated by encephalomyelitis. We investigated EV71 brainstem infection and whether this infection could be ameliorated by passive immunization in a mouse model. Enterovirus 71 was injected into unilateral jaw/facial muscles of 2-week-old mice, and hyperimmune sera were given before or after infection. Harvested tissues were studied by light microscopy, immunohistochemistry, in situ hybridization, and viral titration. In unimmunized mice, viral antigen and RNA were detected within 24 hours after infection only in ipsilateral cranial nerves, motor trigeminal nucleus, reticular formation, and facial nucleus; viral titers were significantly higher in the brainstem than in the spinal cord samples. Mice given preinfection hyperimmune serum showed a marked reduction of ipsilateral viral antigen/RNA and viral titers in the brainstem in a dose-dependent manner. With optimum hyperimmune serum given after infection, brainstem infection was significantly reduced in a time-dependent manner. A delay in disease onset and a reduction of disease severity and mortality were also observed. Thus, EV71 can directly infect the brainstem, including the medulla, via cranial nerves, most likely by retrograde axonal transport. This may explain the sudden cardiorespiratory collapse in human patients with fatal encephalomyelitis. Moreover, our results suggest that passive immunization may still benefit EV71-infected patients who have neurologic complications.
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Tan et al. (2014) studied Enterovirus 71 (EV71) brainstem infection. Hyperimmune sera (passive immunization) vs. Unimmunized mice was evaluated on Brainstem viral antigen/RNA, viral titers, disease onset, severity, and mortality. Passive immunization with hyperimmune sera before or after EV71 infection in mice significantly reduced brainstem viral titers, delayed disease onset, and reduced disease severity and mortality.
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