Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, United States.
Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, United States.
Vaccine. 2019 Feb 28;37(10):1284-1292. doi: 10.1016/j.vaccine.2019.01.055. Epub 2019 Feb 7.
Influenza vaccines are important for prevention of influenza-associated hospitalization. However, the effectiveness of influenza vaccines can vary by year and influenza type and subtype and mechanisms underlying this variation are incompletely understood. Assessments of serologic correlates of protection can support interpretation of influenza vaccine effectiveness in hospitalized populations.
We enrolled adults hospitalized for treatment of acute respiratory illnesses during the 2014-2015 and 2015-2016 influenza seasons whose symptoms began <10 days prior to enrollment. Influenza infection status was determined by RT-PCR. Influenza vaccination status was defined by self-report and medical record/registry documentation. Serum specimens collected at hospital admission were tested in hemagglutination-inhibition (HAI) and neuraminidase-inhibition (NAI) assays. We evaluated how well antibody measured in these specimens represented pre-infection immune status, and measured associations between antibody and influenza vaccination and infection.
Serum specimens were retrieved for 315 participants enrolled during the 2014-2015 season and 339 participants during the 2015-2016 season. Specimens were collected within 3 days of illness onset from 65% of participants. Geometric mean titers (GMTs) did not vary by the number of days from illness onset to specimen collection among influenza positive participants suggesting that measured antibody was representative of pre-infection immune status rather than a de novo response to infection. In both seasons, vaccinated participants had higher HAI and NAI GMTs than unvaccinated. HAI titers against the 2014-2015 A(H3N2) vaccine strain did not correlate with protection from infection with antigenically-drifted A(H3N2) viruses that circulated that season. In contrast, higher HAI titers against the A(H1N1)pdm09 vaccine strain were associated with reduced odds of A(H1N1)pdm09 infection in 2015-2016.
Serum collected shortly after illness onset at hospital admission can be used to assess correlates of protection against influenza infection. Broader implementation of similar studies would provide an opportunity to understand the successes and shortcomings of current influenza vaccines.
流感疫苗对预防与流感相关的住院治疗非常重要。然而,流感疫苗的有效性可能因年份和流感类型及亚型而异,其变化的机制尚不完全清楚。血清学保护相关因素的评估可以支持对住院人群中流感疫苗有效性的解释。
我们纳入了在 2014-2015 年和 2015-2016 年流感季节因急性呼吸道疾病住院治疗且症状在入组前<10 天开始的成年人。通过 RT-PCR 确定流感感染状态。通过自我报告和病历/登记处的记录来定义流感疫苗接种状态。在入院时采集的血清标本在血凝抑制(HAI)和神经氨酸酶抑制(NAI)试验中进行检测。我们评估了这些标本中测量的抗体如何代表感染前的免疫状态,并测量了抗体与流感疫苗接种和感染之间的关联。
共检索到 315 名在 2014-2015 年季节和 339 名在 2015-2016 年季节入组的参与者的血清标本。65%的参与者在发病后 3 天内采集了标本。在流感阳性的参与者中,从发病到采集标本的天数与抗体的几何平均滴度(GMT)没有差异,这表明所测量的抗体代表了感染前的免疫状态,而不是对感染的新的反应。在两个季节中,接种疫苗的参与者的 HAI 和 NAI GMT 均高于未接种疫苗的参与者。针对 2014-2015 年 A(H3N2)疫苗株的 HAI 滴度与该季节流行的具有抗原漂移的 A(H3N2)病毒的感染保护无关。相比之下,在 2015-2016 年,针对 A(H1N1)pdm09 疫苗株的较高 HAI 滴度与 A(H1N1)pdm09 感染的几率降低相关。
在发病后不久在医院采集的血清可以用于评估针对流感感染的保护相关因素。更广泛地实施类似的研究将有机会了解当前流感疫苗的成功和不足。