Virus-induced humoral immunity: on how B cell responses are initiated.

Most antiviral vaccines are based on viral particles, which are efficient inducers of B cell responses. In addition to their ability to replicate, several features associated with the structure and content of the viral particles are responsible for this high immunogenicity. First, viral particles us...

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Main Authors: Zabel, F, Kündig, T, Bachmann, M
Format: Journal article
Language:English
Published: 2013
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author Zabel, F
Kündig, T
Bachmann, M
author_facet Zabel, F
Kündig, T
Bachmann, M
author_sort Zabel, F
collection OXFORD
description Most antiviral vaccines are based on viral particles, which are efficient inducers of B cell responses. In addition to their ability to replicate, several features associated with the structure and content of the viral particles are responsible for this high immunogenicity. First, viral particles usually have dimensions between 20 and 200 nm, a size optimal for drainage to lymph nodes and direct interaction with B cells. Second, the surface of most viral particles is highly repetitive, causing efficient cross-linking of B cell receptors, an early and key step of B cell activation. In addition, such repetitive structures bind natural antibodies and fix complement, further enhancing B cell activation as well as transport to and deposition on follicular dendritic cells. Third, viral particles carry ligands for toll-like receptor 7/8 or 9 which activate B cells directly for isotype switching as well as dendritic cells for T cell priming. In this review, we will highlight recent insights in these mechanisms and discuss their impact on antiviral antibody responses.
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spelling oxford-uuid:4156059c-8ae6-4712-a978-929e8ac237b82022-03-26T14:43:09ZVirus-induced humoral immunity: on how B cell responses are initiated.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:4156059c-8ae6-4712-a978-929e8ac237b8EnglishSymplectic Elements at Oxford2013Zabel, FKündig, TBachmann, MMost antiviral vaccines are based on viral particles, which are efficient inducers of B cell responses. In addition to their ability to replicate, several features associated with the structure and content of the viral particles are responsible for this high immunogenicity. First, viral particles usually have dimensions between 20 and 200 nm, a size optimal for drainage to lymph nodes and direct interaction with B cells. Second, the surface of most viral particles is highly repetitive, causing efficient cross-linking of B cell receptors, an early and key step of B cell activation. In addition, such repetitive structures bind natural antibodies and fix complement, further enhancing B cell activation as well as transport to and deposition on follicular dendritic cells. Third, viral particles carry ligands for toll-like receptor 7/8 or 9 which activate B cells directly for isotype switching as well as dendritic cells for T cell priming. In this review, we will highlight recent insights in these mechanisms and discuss their impact on antiviral antibody responses.
spellingShingle Zabel, F
Kündig, T
Bachmann, M
Virus-induced humoral immunity: on how B cell responses are initiated.
title Virus-induced humoral immunity: on how B cell responses are initiated.
title_full Virus-induced humoral immunity: on how B cell responses are initiated.
title_fullStr Virus-induced humoral immunity: on how B cell responses are initiated.
title_full_unstemmed Virus-induced humoral immunity: on how B cell responses are initiated.
title_short Virus-induced humoral immunity: on how B cell responses are initiated.
title_sort virus induced humoral immunity on how b cell responses are initiated
work_keys_str_mv AT zabelf virusinducedhumoralimmunityonhowbcellresponsesareinitiated
AT kundigt virusinducedhumoralimmunityonhowbcellresponsesareinitiated
AT bachmannm virusinducedhumoralimmunityonhowbcellresponsesareinitiated