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建立一个队列,用于对从普通人群中招募的老年人的流感疫苗免疫反应进行深度表型分析。

Establishment of a cohort for deep phenotyping of the immune response to influenza vaccination among elderly individuals recruited from the general population.

作者信息

Akmatov Manas K, Riese Peggy, May Marcus, Jentsch Leonhard, Ahmed Malik W, Werner Damaris, Rösel Anja, Tyler Megan, Pessler Kevin, Prokein Jana, Bernemann Inga, Klopp Norman, Prochnow Blair, Trittel Stephanie, Tallam Aravind, Illig Thomas, Schindler Christoph, Guzmán Carlos A, Pessler Frank

机构信息

a TWINCORE, Centre for Experimental and Clinical Infection Research , Hannover , Germany.

b Helmholtz Centre for Infection Research , Braunschweig , Germany.

出版信息

Hum Vaccin Immunother. 2017 Jul 3;13(7):1630-1639. doi: 10.1080/21645515.2017.1299300. Epub 2017 Apr 10.

Abstract

Elderly individuals have the highest burden of disease from influenza infection but also the lowest immune response to influenza vaccination. A better understanding of the host response to influenza vaccination in the elderly is therefore urgently needed. We conducted a biphasic prospective, population-based study from Dec. 2014 to May 2015 (pilot study) and Sept. 2015 to May 2016 (main study). Individuals 65-80 y of age were randomly selected from the residents' registration office in Hannover, Germany, for the pilot (n = 34) and main study (n = 200). The pilot study tested recruitment for study arms featuring 2, 4, or 5 visits/blood draws. The 5-visit (day 0, 1/3, 7, 21, 70 with respect to vaccination) study arm was selected for the main study. Both studies featured vaccination with Fluad™ (Novartis, Italy), a detailed medical history, a physical exam, recording of adverse events, completion of a questionnaire on common infections and an end-of-study questionnaire, and blood samples. Response rates in the pilot and main studies were 3.7% and 4.0%, respectively. Willingness to participate did not differ among the study arms (Fisher's exact test, p = 0.44). In both studies, there were no losses to follow-up. Compliance with study visits, blood sampling and completion of the questionnaires was very high (100%, >97%, 100%, respectively), as were participants' acceptance of and satisfaction with both phases of the study. The low response rates indicate the need for optimized recruitment strategies if the study population is to be representative of the general population. Nonetheless, the complex prospective study design proved to be highly feasible.

摘要

老年人感染流感后的疾病负担最重,但对流感疫苗的免疫反应也最低。因此,迫切需要更好地了解老年人对流感疫苗接种的宿主反应。我们在2014年12月至2015年5月(试点研究)以及2015年9月至2016年5月(主要研究)进行了一项双阶段前瞻性、基于人群的研究。从德国汉诺威居民登记办公室随机选取65至80岁的个体参与试点研究(n = 34)和主要研究(n = 200)。试点研究测试了不同访视/采血次数(2次、4次或5次)的研究组招募情况。主要研究选取了5次访视(相对于疫苗接种的第0天、第1/3天、第7天、第21天、第70天)的研究组。两项研究均采用Fluad™(意大利诺华公司)进行疫苗接种,记录详细病史、进行体格检查、记录不良事件、完成关于常见感染的问卷和研究结束时的问卷,并采集血样。试点研究和主要研究的应答率分别为3.7%和4.0%。各研究组的参与意愿无差异(Fisher精确检验,p = 0.44)。两项研究均无失访情况。对研究访视、采血和问卷完成情况的依从性非常高(分别为100%、>97%、100%),参与者对研究两个阶段的接受度和满意度也很高。低应答率表明,如果研究人群要代表一般人群,就需要优化招募策略。尽管如此,复杂的前瞻性研究设计证明是高度可行的。

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