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Tytuł pozycji:

Recalling the Future: Immunological Memory Toward Unpredictable Influenza Viruses

Tytuł:
Recalling the Future: Immunological Memory Toward Unpredictable Influenza Viruses
Autorzy:
Maria Auladell
Xiaoxiao Jia
Luca Hensen
Brendon Chua
Annette Fox
Thi H. O. Nguyen
Peter C. Doherty
Katherine Kedzierska
Temat:
T cells
B cells
influenza
immunological memory
vaccine
Immunologic diseases. Allergy
RC581-607
Źródło:
Frontiers in Immunology, Vol 10 (2019)
Wydawca:
Frontiers Media S.A., 2019.
Rok publikacji:
2019
Kolekcja:
LCC:Immunologic diseases. Allergy
Typ dokumentu:
article
Opis pliku:
electronic resource
Język:
English
ISSN:
1664-3224
Relacje:
https://www.frontiersin.org/article/10.3389/fimmu.2019.01400/full; https://doaj.org/toc/1664-3224
DOI:
10.3389/fimmu.2019.01400
Dostęp URL:
https://doaj.org/article/9ae90ff6752c4f95ab3ee7623a0080bd  Link otwiera się w nowym oknie
Numer akcesji:
edsdoj.9ae90ff6752c4f95ab3ee7623a0080bd
Czasopismo naukowe
Persistent and durable immunological memory forms the basis of any successful vaccination protocol. Generation of pre-existing memory B cell and T cell pools is thus the key for maintaining protective immunity to seasonal, pandemic and avian influenza viruses. Long-lived antibody secreting cells (ASCs) are responsible for maintaining antibody levels in peripheral blood. Generated with CD4+ T help after naïve B cell precursors encounter their cognate antigen, the linked processes of differentiation (including Ig class switching) and proliferation also give rise to memory B cells, which then can change rapidly to ASC status after subsequent influenza encounters. Given that influenza viruses evolve rapidly as a consequence of antibody-driven mutational change (antigenic drift), the current influenza vaccines need to be reformulated frequently and annual vaccination is recommended. Without that process of regular renewal, they provide little protection against “drifted” (particularly H3N2) variants and are mainly ineffective when a novel pandemic (2009 A/H1N1 “swine” flu) strain suddenly emerges. Such limitation of antibody-mediated protection might be circumvented, at least in part, by adding a novel vaccine component that promotes cross-reactive CD8+ T cells specific for conserved viral peptides, presented by widely distributed HLA types. Such “memory” cytotoxic T lymphocytes (CTLs) can rapidly be recalled to CTL effector status. Here, we review how B cells and follicular T cells are elicited following influenza vaccination and how they survive into a long-term memory. We describe how CD8+ CTL memory is established following influenza virus infection, and how a robust CTL recall response can lead to more rapid virus elimination by destroying virus-infected cells, and recovery. Exploiting long-term, cross-reactive CTL against the continuously evolving and unpredictable influenza viruses provides a possible mechanism for preventing a disastrous pandemic comparable to the 1918-1919 H1N1 “Spanish flu,” which killed more than 50 million people worldwide.

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