Rentier Bernard, Gershon Anne A
Fundamental Virology Unit, University of Liége, Belgium.
Pediatr Infect Dis J. 2004 May;23(5):379-89. doi: 10.1097/01.inf.0000122606.88429.8f.
The seriousness of varicella-zoster virus (VZV) infection as a public health issue is becoming clearer as country-specific epidemiologic and pharmacoeconomic data become available. In Germany, for example, studies have shown that >5.5% of immunologically healthy individuals develop varicella-related complications such as bacterial superinfections, acute neurologic disorders, pneumonia, bronchitis and otitis media; whereas in Italy, 3.5 to 5% of childhood cases of varicella cause complications such as upper respiratory tract and cutaneous infections. Varicella vaccines are now available. These live attenuated Oka strain vaccines have been shown in extensive studies to be highly immunogenic and well-tolerated in immunocompetent and immunocompromised children, with seroconversion rates ranging from 94 to 100% and 53 to 100%, respectively. These vaccines are also highly effective against clinical disease. These considerations led to a reevaluation of varicella vaccination policies. A routine varicella vaccination program targeting healthy children has already been implemented in the US, and data produced are encouraging and valuable. Similar strategies have not yet been adopted across Europe. The European Working Group on Varicella (EuroVar) was formed in 1998 to address the issues surrounding varicella epidemiology in Europe. After a series of meetings, the EuroVar members prepared a consensus statement recommending routine varicella vaccination for all healthy children between 12 and 18 months and to all susceptible children before their 13th birthday, in addition to catch-up vaccination in older children and adults who have no reliable history of varicella and who are at high risk of transmission and exposure. However, such a policy is recommended only if a very high coverage rate can be achieved. This could be reached with a measles-mumps-rubella-varicella combined vaccine.
随着各国具体的流行病学和药物经济学数据不断涌现,水痘带状疱疹病毒(VZV)感染作为一个公共卫生问题的严重性日益凸显。例如,在德国,研究表明,超过5.5%免疫功能正常的个体出现与水痘相关的并发症,如细菌重叠感染、急性神经紊乱、肺炎、支气管炎和中耳炎;而在意大利,3.5%至5%的儿童水痘病例会引发诸如上呼吸道和皮肤感染等并发症。水痘疫苗现已面市。这些减毒活Oka株疫苗在大量研究中已证明,在免疫功能正常和免疫功能低下的儿童中具有高度免疫原性且耐受性良好,血清转化率分别为94%至100%和53%至100%。这些疫苗对临床疾病也具有高度有效性。这些因素促使人们对水痘疫苗接种政策进行重新评估。美国已经实施了针对健康儿童的常规水痘疫苗接种计划,所产生的数据令人鼓舞且很有价值。欧洲尚未采取类似策略。欧洲水痘工作组(EuroVar)于1998年成立,旨在解决欧洲水痘流行病学相关问题。经过一系列会议后,EuroVar成员起草了一份共识声明,建议对所有12至18个月的健康儿童以及所有13岁生日前的易感儿童进行常规水痘疫苗接种,此外,对没有可靠水痘病史且传播和接触风险高的大龄儿童及成人进行补种。然而,只有在能够实现非常高的接种率时,才建议实施这样的政策。这可以通过麻疹-腮腺炎-风疹-水痘联合疫苗来实现。