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J Child Neurol. 2019 Jan 10:883073818821498. doi: 10.1177/0883073818821498. [Epub ahead of print]

Severe Herpes Zoster Following Varicella Vaccination in Immunocompetent Young Children.

Author information

1
1 Division of Infectious Diseases, Blank Children's Hospital, Des Moines, IA, USA.
2
2 Department of Pediatrics, McFarland Clinic, Ames, IA, USA.
3
3 Division of Infectious Diseases/Virology, Children's Hospital, University of Iowa, Iowa City, IA, USA.
4
4 Division of Child Neurology, Children's Hospital, University of Iowa, Iowa City, IA, USA.

Abstract

Varicella vaccination is now virtually universal in North America, as well as in some European and Asian countries. Since varicella vaccine is a live attenuated virus, the virus replicates in the skin after administration and can travel via sensory nerves or viremia to become latent in the dorsal root ganglia. In some immunized children, virus reactivates within a few months to a few years to cause the dermatomal exanthem known as herpes zoster (shingles). Herpes zoster caused by vaccine virus often reactivates within the same dermatome as the site of the original varicella vaccine injection. We present evidence that occasional cases of herpes zoster following varicella vaccination in immunocompetent children can be as severe as herpes zoster following wild-type varicella. Analysis of the virus in one case disclosed that the vaccine virus causing herpes zoster was a wild-type variant with a mutation in ORF0. With regard to dermatomal localization of the viral eruption, we predict that herpes zoster of the lumbar dermatomes in children is likely to be caused by vaccine virus, because herpes zoster in those dermatomes is rare in children after wild-type varicella. One of the children with herpes zoster subsequently developed asthma, a known risk factor for herpes zoster, but none of the children had an autoimmune disease. Although postherpetic neuralgia is exceedingly rare, children who develop herpes zoster following varicella vaccination are at risk (albeit low) of developing meningoencephalitis and should be carefully observed for a few weeks.

KEYWORDS:

Oka vaccine; acyclovir; asthma; encephalitis; open reading frame 0; sequencing; shingles; varicella-zoster virus

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