血凝素(流感)
免疫原
免疫
接种疫苗
生物
病毒学
干细胞
表位
A组
抗原漂移
抗原
B组
H5N1亚型流感病毒
免疫学
抗体
遗传学
医学
单克隆抗体
病毒
内科学
作者
Sarah F. Andrews,Michael Joyce,Michael Chambers,Rebecca A. Gillespie,Masaru Kanekiyo,Kwanyee Leung,Eun Sung Yang,Yaroslav Tsybovsky,Adam K. Wheatley,Michelle C. Crank,Jeffrey C. Boyington,Madhu Prabhakaran,Sandeep Narpala,Xuejun Chen,Robert T. Bailer,Grace Chen,Emily E. Coates,Peter D. Kwong,Richard A. Koup,John R. Mascola
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2017-07-21
卷期号:2 (13)
被引量:116
标识
DOI:10.1126/sciimmunol.aan2676
摘要
Antigenic drift and shift of influenza strains underscore the need for broadly protective influenza vaccines. One strategy is to design immunogens that elicit B cell responses against conserved epitopes on the hemagglutinin (HA) stem. To better understand the elicitation of HA stem-targeted B cells to group 1 and group 2 influenza subtypes, we compared the memory B cell response to group 2 H7N9 and group 1 H5N1 vaccines in humans. Upon H7N9 vaccination, almost half of the HA stem-specific response recognized the group 1 and group 2 subtypes, whereas the response to H5N1 was largely group 1-specific. Immunoglobulin repertoire analysis of HA-specific B cells indicated that the H7N9 and H5N1 vaccines induced genetically similar cross-group HA stem-binding B cells, albeit at a much higher frequency upon H7N9 vaccination. These data suggest that a group 2-based stem immunogen could prove more effective than a group 1 immunogen at eliciting broad cross-group protection in humans.
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