Bundeswehr Institute of Microbiology, German National Reference Laboratory for TBEV, Munich, Germany.
Institute of Medical Biometry and Statistics, Faculty of Medicine and Medical Centre - University of Freiburg, Freiburg, Germany.
Clin Microbiol Infect. 2020 Aug;26(8):1090.e7-1090.e13. doi: 10.1016/j.cmi.2019.12.001. Epub 2019 Dec 13.
There are few data available regarding the clinical course of tick-borne encephalitis virus (TBEV) vaccination breakthrough infections. The published studies suggest that vaccination breakthrough infections may have a more severe course than native TBEV infection in unvaccinated individuals-potentially due to antibody-dependent enhancement. Here we report a large analysis of vaccination breakthrough infections.
This retrospective analysis was based on a national surveillance dataset spanning the years 2001-2018. Variables reflecting disease severity, such as 'CNS symptoms', 'myelitis', 'fatal outcome' and 'hospitalization' were analysed as well as general epidemiological variables. Cases were categorized as 'unvaccinated' or 'ever vaccinated', the latter category including cases with at least one dose of a TBEV vaccine.
A total of 6073 notified TBEV infection cases were included in our analysis. Sufficient data on vaccination status were available for 95.1% of patients (5777/6073); of these, 5298 presented with a native infection. A total of (334/5777) cases developed an infection despite having been vaccinated at least once. Comparing unvaccinated patients with those with at least one vaccination, we find an odds ratio (OR) 2.73, (95% confidence interval (CI) 0.79-9.50) regarding the variable fatal outcome that did not reach statistical significance. Analysing the clinical variables 'CNS symptoms' and 'myelitis', there is no difference between these groups (OR 0.86, 95% CI 0.68-1.08; and OR 1.30, 95% CI 0.74-2.27 respectively). Patients who were vaccinated and had an assumed protection at symptom onset (n = 100) had a higher risk for the development of myelitic symptoms (OR 2.21, 95% CI 1.01-4.86]) than unvaccinated patients.
Our findings could neither verify that vaccination breakthrough infections might cause a more severe disease than native infections nor prove a clear antibody-dependent enhancement phenomenon. It remains unclear whether the increased myelitis risk in a subgroup of vaccinated patients is a true effect or confounded.
关于蜱传脑炎病毒(TBEV)疫苗突破性感染的临床病程,目前数据有限。已发表的研究表明,疫苗突破性感染可能比未接种疫苗的个体中的原生 TBEV 感染更严重-可能是由于抗体依赖性增强作用所致。在这里,我们报告了一项对疫苗突破性感染的大型分析。
这项回顾性分析基于 2001-2018 年的国家监测数据集。分析了反映疾病严重程度的变量,例如“CNS 症状”、“脊髓炎”、“致命结局”和“住院”,以及一般流行病学变量。病例分为“未接种”或“曾接种”,后者包括至少接种过一剂 TBEV 疫苗的病例。
我们的分析共纳入了 6073 例通报的 TBEV 感染病例。有足够数据可用于 95.1%(5777/6073)的患者接种状态;其中,5298 例为原生感染。在 5777 例中,共有 334 例尽管至少接种过一次疫苗,但仍发生了感染。与未接种疫苗的患者相比,我们发现有统计学意义的致命结局变量的比值比(OR)为 2.73(95%置信区间(CI)为 0.79-9.50)。分析“CNS 症状”和“脊髓炎”这两个临床变量,两组之间没有差异(OR 0.86,95%CI 0.68-1.08;和 OR 1.30,95%CI 0.74-2.27)。在症状发作时假定具有保护作用而接种疫苗的患者(n=100)发生脊髓炎症状的风险更高(OR 2.21,95%CI 1.01-4.86)。
我们的发现既不能证实疫苗突破性感染可能比原生感染引起更严重的疾病,也不能证明明确的抗体依赖性增强现象。在接种疫苗的患者亚组中,髓炎风险增加是否是真正的影响还是混杂因素仍不清楚。