| Literature DB >> 32792465 |
Carl W Davis1,2, Katherine J L Jackson3, Megan M McCausland1,2, Jaime Darce4, Cathy Chang1,2, Susanne L Linderman1,2, Chakravarthy Chennareddy1,2, Rebecca Gerkin2,5, Shantoria J Brown2,5, Jens Wrammert1,6, Aneesh K Mehta2,7, Wan Cheung Cheung4, Scott D Boyd3, Edmund K Waller2,5, Rafi Ahmed8,2.
Abstract
A universal vaccine against influenza would ideally generate protective immune responses that are not only broadly reactive against multiple influenza strains but also long-lasting. Because long-term serum antibody levels are maintained by bone marrow plasma cells (BMPCs), we investigated the production and maintenance of these cells after influenza vaccination. We found increased numbers of influenza-specific BMPCs 4 weeks after immunization with the seasonal inactivated influenza vaccine, but numbers returned to near their prevaccination levels after 1 year. This decline was driven by the loss of BMPCs induced by the vaccine, whereas preexisting BMPCs were maintained. Our results suggest that most BMPCs generated by influenza vaccination in adults are short-lived. Designing strategies to enhance their persistence will be a key challenge for the next generation of influenza vaccines.Entities:
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Year: 2020 PMID: 32792465 DOI: 10.1126/science.aaz8432
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728