| Literature DB >> 31231764 |
Sarah Leach1,2, Ryo Shinnakasu2, Yu Adachi3, Masatoshi Momota4, Chieko Makino-Okamura5, Takuya Yamamoto6, Ken J Ishii4, Hidehiro Fukuyama5, Yoshimasa Takahashi3, Tomohiro Kurosaki1,2,5.
Abstract
While two memory compartments, memory B cells and long-lived plasma cells, are thought to contribute to the successful establishment of memory recall responses, the unique roles of each cellular compartment are still unclear. Herein, by tracing influenza anti-hemagglutinin (HA)-specific antibodies in mice, we demonstrate that pre-existing antibodies secreted by long-lived plasma cells are essential for protection from reinfection with the same influenza virus, whereas protection from secondary infection with an antigenically distinct influenza virus requires memory B-cell activation. These activated memory B cells were largely specific for the conserved HA stem region, and generated sufficient levels of antibodies for protection from heterologous reinfection. Given that the anti-stem plasmablasts derived from the memory B cells were higher affinity than those from naive B cells, our results suggest that maturation of anti-stem memory B cells during primary influenza infection and their subsequent activation are required for protection from reinfection by mutant viruses. © The Japanese Society for Immunology. 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.Entities:
Keywords: antibody; cross-reactive; immunity; infection; virus
Mesh:
Year: 2019 PMID: 31231764 DOI: 10.1093/intimm/dxz049
Source DB: PubMed Journal: Int Immunol ISSN: 0953-8178 Impact factor: 4.823