Major Infectious Disease Control Key Laboratory, The Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
Division of Biostatistics, JC School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong SAR, China; The CUHK Shenzhen Research Institute, Shenzhen, China.
J Infect. 2016 Mar;72(3):369-76. doi: 10.1016/j.jinf.2015.12.013. Epub 2015 Dec 30.
This study aimed to elucidate the antibody response pattern of multiple influenza subtypes through a 4-year serological study of a general population in Shenzhen, Southern China.
A serial cross-sectional serological survey was conducted at eight time points between 2009 and 2012. A total number of 5876 subjects were recruited from all age groups. The influenza subtypes tested were A/H1N1, A/H3N2, B/Yamagata, B/Victoria, and A/H1N1pdm. Genetic sequencing and phylogenetic analysis were performed on 127 H3 genes and 28 H1pdm genes.
We found concurrent epidemics of A/H3N2 and A/H1N1pdm with simultaneous peak times at March 2011. A/H3N2 was the dominant subtype. Ten residue substitutions (S61N, T64I, K78E, K160N, N161S, A214S, T228A, A229V, V239I, N294K, and N328S) were found in the H3 gene that might underlie its epidemic. The elderly group showed an antibody response cycle that was weaker in magnitude and slower in peak time than in younger groups.
The study provides a broad transmission picture and epidemiological characteristics of the major flu subtypes. The findings suggest that it may be necessary to include the A/H1N1pdm strain to the current trivalent or quadrivalent vaccine design. The delayed antibody response cycle in the elderly group indicates the need for better protection of elderly people that might be achieved by an earlier vaccination at a higher dose.
本研究旨在通过对中国南方深圳的一般人群进行为期 4 年的血清学研究,阐明多种流感亚型的抗体反应模式。
在 2009 年至 2012 年期间,我们进行了 8 个时间点的连续横断面血清学调查。共招募了来自所有年龄段的 5876 名受试者。检测的流感亚型为 A/H1N1、A/H3N2、B/Yamagata、B/Victoria 和 A/H1N1pdm。对 127 个 H3 基因和 28 个 H1pdm 基因进行了基因测序和系统进化分析。
我们发现 A/H3N2 和 A/H1N1pdm 同时流行,且在 2011 年 3 月同时达到高峰。A/H3N2 是主要亚型。在 H3 基因中发现了 10 个残基替换(S61N、T64I、K78E、K160N、N161S、A214S、T228A、A229V、V239I、N294K 和 N328S),可能是其流行的基础。老年组的抗体反应周期在幅度和峰值时间上均比年轻组弱。
本研究提供了主要流感亚型的广泛传播情况和流行病学特征。研究结果表明,可能需要在当前的三价或四价疫苗设计中加入 A/H1N1pdm 株。老年组抗体反应周期延迟表明,需要更好地保护老年人,可能通过更高剂量的早期疫苗接种来实现。