Department of Pediatrics, Konan Kosei Hospital, 137 Ohmatsubara, Takaya-cho, Konan, Aichi, Japan.
J Infect Chemother. 2013 Apr;19(2):188-95. doi: 10.1007/s10156-013-0577-x. Epub 2013 Mar 13.
Varicella-zoster virus (VZV) is the causative agent of varicella (chickenpox). It shows extremely high infectivity and is spread by airborne, droplet, and contact transmission. After a person is infected with VZV, the virus remains dormant in the dorsal root ganglia, but can be reactivated under circumstances where specific immunity declines, leading to the development of herpes zoster (shingles). Although varicella is a disease that usually resolves after about 1 week, it can cause various complications such as secondary bacterial skin infection, pneumonia, and encephalitis. In addition, varicella can become severe in immunocompromised persons, whereas VZV infection transmitted from an infected mother can cause the congenital varicella syndrome or serious neonatal varicella. In 1974, a live varicella vaccine (Oka strain) was developed in Japan for the prevention of varicella, and clinical trials performed during the development were mainly focused on high-risk children. In 1985, the Oka strain was recognized as the best varicella vaccine strain by the World Health Organization (WHO). Today, all the varicella vaccines used worldwide to immunize approximately 32 million people annually contain the Oka strain. In Japan, it has been commercially available since 1987 for the voluntary vaccination program, in which children over the age of 1 year with no history of previous varicella infection receive a single dose. In addition to healthy children, this vaccine can be used for immunocompromised children, and vaccination of elderly persons can also be done to enhance their immunity against VZV. Varicella vaccine is a highly safe vaccine with sufficient immunogenicity. The preventive effect of single-dose vaccination is believed to be approximately 80 % for all types of varicella, including mild cases; it is 95 % or greater for moderate to severe disease. Implementation of a two-dose vaccination schedule has proved to be effective against breakthrough varicella, which is observed in approximately 20-30 % of children vaccinated with a single dose. Because it is administered as part of the voluntary vaccination program, the varicella vaccination coverage rate in Japan has remained low until recently at around 20-30 %, with no sign of a decrease in the number of varicella patients. It is necessary to maintain a vaccination rate of 90 % or higher to prevent varicella epidemics. To achieve this goal, implementation of a routine vaccination program for varicella and introduction of a two-dose vaccination schedule, which is more effective than a single-dose schedule, would be highly desirable.
水痘-带状疱疹病毒(VZV)是水痘(带状疱疹)的病原体。它具有极高的传染性,通过空气飞沫、飞沫和接触传播。人感染 VZV 后,病毒潜伏在背根神经节,但在特定免疫力下降的情况下会被重新激活,导致带状疱疹(带状疱疹)的发生。虽然水痘通常在大约 1 周后自行痊愈,但它可能导致各种并发症,如继发细菌皮肤感染、肺炎和脑炎。此外,免疫功能低下者的水痘可能会变得严重,而从受感染母亲传播的 VZV 感染可导致先天性水痘综合征或严重的新生儿水痘。1974 年,日本开发了一种活水痘疫苗(Oka 株)用于预防水痘,开发过程中的临床试验主要针对高危儿童。1985 年,世界卫生组织(WHO)将 Oka 株确认为最佳水痘疫苗株。如今,全世界用于免疫接种约 3200 万人的所有水痘疫苗均含有 Oka 株。在日本,自 1987 年以来,该疫苗一直作为自愿接种计划中的商业产品供应,1 岁以上无既往水痘感染史的儿童接种一剂。除了健康儿童,该疫苗也可用于免疫功能低下的儿童,为增强老年人对 VZV 的免疫力也可对其进行接种。水痘疫苗是一种具有足够免疫原性的高度安全疫苗。单剂接种的预防效果被认为对所有类型的水痘(包括轻症)约为 80%;对中重度疾病的预防效果为 95%或更高。两剂接种方案的实施已被证明可有效预防突破性水痘,约 20-30%接种一剂的儿童会出现突破性水痘。由于它是作为自愿接种计划的一部分接种的,因此直到最近,日本的水痘疫苗接种率一直保持在 20-30%左右,没有下降的迹象。要预防水痘流行,需要保持 90%或更高的疫苗接种率。为实现这一目标,实施水痘常规疫苗接种计划并引入比单剂接种方案更有效的两剂接种方案将是非常理想的。