British Columbia Centre for Disease Control, Canada.
J Infect Dis. 2012 Jun 15;205(12):1858-68. doi: 10.1093/infdis/jis283. Epub 2012 Apr 9.
To estimate influenza vaccine effectiveness (VE) for the 2007-2008 season and assess the sentinel surveillance system in Canada for monitoring virus evolution and impact on VE.
Nasal/nasopharyngeal swabs and epidemiologic details were collected from patients presenting to a sentinel physician within 7 days of influenza-like illness onset. Cases tested positive for influenza A/B virus by real-time polymerase chain reaction; controls tested negative. Hemagglutination inhibition (HI) and gene sequencing explored virus relatedness to vaccine. VE was calculated as 1 minus the odds ratio for influenza in vaccinated versus nonvaccinated participants, with adjustment for confounders.
Of 1425 participants, 21% were vaccinated. Influenza virus was detected in 689 (48%), of which isolates from 663 were typed/subtyped: 189 (29%) were A/H1, 210 (32%) were A/H3, and 264 (40%) were B. Of A/H1N1 isolates, 6% showed minor HI antigenic mismatch to vaccine, with greater variation based on genetic identity. All A/H3N2 isolates showed moderate antigenic mismatch, and 98% of influenza B virus isolates showed major lineage-level mismatch to vaccine. Adjusted VE for A/H1N1, A/H3N2, and B components was 69% (95% confidence interval [CI], 44%-83%), 57% (95% CI, 32%-73%), and 55% (95% CI, 32%-70%), respectively, with an overall VE of 60% (95% CI, 45%-71%).
Detailed antigenic and genotypic analysis of influenza viruses was consistent with epidemiologic estimates of VE showing cross-protection. A routine sentinel surveillance system that combines detailed virus and VE monitoring annually, as modeled in Canada, may guide improved vaccine selection and protection.
评估 2007-2008 年流感疫苗的有效性(VE),并评估加拿大的哨点监测系统,以监测病毒的演变及其对 VE 的影响。
从流感样疾病发病后 7 天内就诊于哨点医生的患者中采集鼻/鼻咽拭子和流行病学详细信息。通过实时聚合酶链反应检测患者的流感 A/B 病毒呈阳性;对照组检测结果为阴性。血凝抑制(HI)和基因测序用于探索病毒与疫苗的相关性。VE 计算为接种组与未接种组中流感的比值的倒数,调整混杂因素。
在 1425 名参与者中,21%的参与者接种了疫苗。在 689 名(48%)参与者中检测到流感病毒,其中 663 个分离株被分型/亚型:189 个(29%)为 A/H1,210 个(32%)为 A/H3,264 个(40%)为 B。A/H1N1 分离株中,6%的分离株与疫苗存在轻微的 HI 抗原错配,而基于遗传同一性的差异更大。所有 A/H3N2 分离株均显示中度抗原错配,98%的流感 B 病毒分离株与疫苗主要谱系水平不匹配。A/H1N1、A/H3N2 和 B 成分的调整 VE 分别为 69%(95%置信区间[CI],44%-83%)、57%(95% CI,32%-73%)和 55%(95% CI,32%-70%),总体 VE 为 60%(95% CI,45%-71%)。
对流感病毒的详细抗原和基因型分析与 VE 的流行病学估计一致,表明存在交叉保护。如加拿大所建模的,一种常规的哨点监测系统,每年结合详细的病毒和 VE 监测,可以指导改进疫苗选择和保护。