Oka strain of varicella zoster virus (VZV) was isolated from vesicles of a 3-year-boy who had developed typical varicella symptoms. It was passaged 11 times in human embryonic lung fibroblasts (HEL) at a rather low temperature of 34°C and 12 times in guinea pig embryo fibroblasts (GPEF) at 37°C. GPEF was the only susceptible non-primate cells; where in some degree of viral replication was noticed. The resultant virus was somewhat temperature sensitive (virus titer at 38°C is lower than that of parental virus), and showed host dependency (more affinity to GPEF); the ratio of virus titer in GPEF/HEL was higher than parental virus. The passaged virus was used as a candidate varicella vaccine and was found safe and effective in normal children and in immunocompromised children with good protective immunity.
Oka varicella vaccine strain was provided to Merck (USA) and RIT-SKF (currently GSK, UK) and licensed in 1984 for high risk children in several countries in Europe by RIT-SKF, then in Japan in 1986 for normal children as well as high risk children, followed by Korea in 1988 similarly as in Japan. In 1995, universal immunization was approved in the USA. Currently, Oka varicella vaccine is widely approved and used throughout the world.
In follow-up of vaccinated children with acute leukemia, the incidence of zoster was fewer in those with no rash after vaccination as compared with those who were rash positive. (5/247 [2.0%] versus 13/83 [15.7%]). Similar results were noted by the US Study Group on varicella vaccine. Usually, no or few rash appears in normal children. From the viewpoint of pathogenesis of herpes zoster, it may be expected that the incidence of herpes zoster would be lower in vaccine recipients in future as compared with those experieing natural varicella.
In 2003, it was recognized in Japan that immunization of elderly individuals with commercially available varicella vaccine (≥30, 000 PFU/dose) enhanced their immunity against VZV, particularly cell-mediated immunity. Hence elderly patients with decreased cell-mediated immunity against VZV were added as the target subjects of varicella vaccination. It was reported in the USA in 2005 that immunization of older adults with high-titered (mostly 32, 000 PFU/dose) varicella vaccine resulted in 61-66% preventive effect of herpes zoster and postherpetic neuralgia (PHN).
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