| Literature DB >> 29625056 |
Yao-Qing Chen1, Teddy John Wohlbold2, Nai-Ying Zheng1, Min Huang1, Yunping Huang1, Karlynn E Neu3, Jiwon Lee4, Hongquan Wan5, Karla Thatcher Rojas1, Ericka Kirkpatrick2, Carole Henry1, Anna-Karin E Palm1, Christopher T Stamper3, Linda Yu-Ling Lan3, David J Topham6, John Treanor7, Jens Wrammert8, Rafi Ahmed8, Maryna C Eichelberger5, George Georgiou4, Florian Krammer9, Patrick C Wilson10.
Abstract
Antibodies to the hemagglutinin (HA) and neuraminidase (NA) glycoproteins are the major mediators of protection against influenza virus infection. Here, we report that current influenza vaccines poorly display key NA epitopes and rarely induce NA-reactive B cells. Conversely, influenza virus infection induces NA-reactive B cells at a frequency that approaches (H1N1) or exceeds (H3N2) that of HA-reactive B cells. NA-reactive antibodies display broad binding activity spanning the entire history of influenza A virus circulation in humans, including the original pandemic strains of both H1N1 and H3N2 subtypes. The antibodies robustly inhibit the enzymatic activity of NA, including oseltamivir-resistant variants, and provide robust prophylactic protection, including against avian H5N1 viruses, in vivo. When used therapeutically, NA-reactive antibodies protected mice from lethal influenza virus challenge even 48 hr post infection. These findings strongly suggest that influenza vaccines should be optimized to improve targeting of NA for durable and broad protection against divergent influenza strains.Entities:
Keywords: B cell; human immunology; humoral immune response; influenza; monoclonal antibody; neuraminidase; therapeutics; vaccine; virus infection
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Year: 2018 PMID: 29625056 PMCID: PMC5890936 DOI: 10.1016/j.cell.2018.03.030
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582