Antibody avidity, persistence, and response to antigen recall: comparison of vaccine adjuvants
Abstract Differences in innate immune ‘imprinting’ between vaccine adjuvants may mediate dissimilar effects on the quantity/quality of persisting adaptive responses. We compared antibody avidity maturation, antibody/memory B cell/CD4+ T cell response durability, and recall responses to non-adjuvante...
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2021
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oai:doaj.org-article:44c6adaabe024a3786359666e5ee13fc2021-12-02T15:52:54ZAntibody avidity, persistence, and response to antigen recall: comparison of vaccine adjuvants10.1038/s41541-021-00337-02059-0105https://doaj.org/article/44c6adaabe024a3786359666e5ee13fc2021-05-01T00:00:00Zhttps://doi.org/10.1038/s41541-021-00337-0https://doaj.org/toc/2059-0105Abstract Differences in innate immune ‘imprinting’ between vaccine adjuvants may mediate dissimilar effects on the quantity/quality of persisting adaptive responses. We compared antibody avidity maturation, antibody/memory B cell/CD4+ T cell response durability, and recall responses to non-adjuvanted fractional-dose antigen administered 1-year post-immunization (Day [D]360), between hepatitis B vaccines containing Adjuvant System (AS)01B, AS01E, AS03, AS04, or Alum (NCT00805389). Both the antibody and B cell levels ranked similarly (AS01B/E/AS03 > AS04 > Alum) at peak response, at D360, and following their increases post-antigen recall (D390). Proportions of high-avidity antibodies increased post-dose 2 across all groups and persisted at D360, but avidity maturation appeared to be more strongly promoted by AS vs. Alum. Post-antigen recall, frequencies of subjects with high-avidity antibodies increased only markedly in the AS groups. Among the AS, total antibody responses were lowest for AS04. However, proportions of high-avidity antibodies were similar between groups, suggesting that MPL in AS04 contributes to avidity maturation. Specific combinations of immunoenhancers in the AS, regardless of their individual nature, increase antibody persistence and avidity maturation.Sonia BudroniFrancesca BuricchiAndrea CavallonePatricia BourguignonMagalie CaubetVincent DewarUgo D’OroOretta FincoNathalie GarçonMohamed El IdrissiMichel JanssensGeert Leroux-RoelsArnaud MarchantTino SchwarzPierre Van DammeGianfranco VolpiniRobbert van der MostArnaud M. DidierlaurentWivine BurnyNature PortfolioarticleImmunologic diseases. AllergyRC581-607Neoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENnpj Vaccines, Vol 6, Iss 1, Pp 1-11 (2021) |
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Immunologic diseases. Allergy RC581-607 Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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Immunologic diseases. Allergy RC581-607 Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Sonia Budroni Francesca Buricchi Andrea Cavallone Patricia Bourguignon Magalie Caubet Vincent Dewar Ugo D’Oro Oretta Finco Nathalie Garçon Mohamed El Idrissi Michel Janssens Geert Leroux-Roels Arnaud Marchant Tino Schwarz Pierre Van Damme Gianfranco Volpini Robbert van der Most Arnaud M. Didierlaurent Wivine Burny Antibody avidity, persistence, and response to antigen recall: comparison of vaccine adjuvants |
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Abstract Differences in innate immune ‘imprinting’ between vaccine adjuvants may mediate dissimilar effects on the quantity/quality of persisting adaptive responses. We compared antibody avidity maturation, antibody/memory B cell/CD4+ T cell response durability, and recall responses to non-adjuvanted fractional-dose antigen administered 1-year post-immunization (Day [D]360), between hepatitis B vaccines containing Adjuvant System (AS)01B, AS01E, AS03, AS04, or Alum (NCT00805389). Both the antibody and B cell levels ranked similarly (AS01B/E/AS03 > AS04 > Alum) at peak response, at D360, and following their increases post-antigen recall (D390). Proportions of high-avidity antibodies increased post-dose 2 across all groups and persisted at D360, but avidity maturation appeared to be more strongly promoted by AS vs. Alum. Post-antigen recall, frequencies of subjects with high-avidity antibodies increased only markedly in the AS groups. Among the AS, total antibody responses were lowest for AS04. However, proportions of high-avidity antibodies were similar between groups, suggesting that MPL in AS04 contributes to avidity maturation. Specific combinations of immunoenhancers in the AS, regardless of their individual nature, increase antibody persistence and avidity maturation. |
format |
article |
author |
Sonia Budroni Francesca Buricchi Andrea Cavallone Patricia Bourguignon Magalie Caubet Vincent Dewar Ugo D’Oro Oretta Finco Nathalie Garçon Mohamed El Idrissi Michel Janssens Geert Leroux-Roels Arnaud Marchant Tino Schwarz Pierre Van Damme Gianfranco Volpini Robbert van der Most Arnaud M. Didierlaurent Wivine Burny |
author_facet |
Sonia Budroni Francesca Buricchi Andrea Cavallone Patricia Bourguignon Magalie Caubet Vincent Dewar Ugo D’Oro Oretta Finco Nathalie Garçon Mohamed El Idrissi Michel Janssens Geert Leroux-Roels Arnaud Marchant Tino Schwarz Pierre Van Damme Gianfranco Volpini Robbert van der Most Arnaud M. Didierlaurent Wivine Burny |
author_sort |
Sonia Budroni |
title |
Antibody avidity, persistence, and response to antigen recall: comparison of vaccine adjuvants |
title_short |
Antibody avidity, persistence, and response to antigen recall: comparison of vaccine adjuvants |
title_full |
Antibody avidity, persistence, and response to antigen recall: comparison of vaccine adjuvants |
title_fullStr |
Antibody avidity, persistence, and response to antigen recall: comparison of vaccine adjuvants |
title_full_unstemmed |
Antibody avidity, persistence, and response to antigen recall: comparison of vaccine adjuvants |
title_sort |
antibody avidity, persistence, and response to antigen recall: comparison of vaccine adjuvants |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/44c6adaabe024a3786359666e5ee13fc |
work_keys_str_mv |
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