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Plasmablast, Memory B Cell, CD4+ T Cell, and Circulating Follicular Helper T Cell Responses to a Non-Replicating Modified Vaccinia Ankara Vaccine

Background: Vaccinia is known to induce antibody and cellular responses. Plasmablast, circulating follicular helper T (cT(FH)) cells, cytokine-expressing CD4 T cells, and memory B cells were compared between subcutaneous (SC) and needle-free jet injection (JI) recipients of non-replicating modified...

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Autores principales: Anderson, Evan J., Lai, Lilin, Wrammert, Jens, Kabbani, Sarah, Xu, Yongxian, Priyamvada, Lalita, Hill, Heather, Goll, Johannes B., Jensen, Travis L., Kao, Carol, Yildirim, Inci, Rouphael, Nadine, Jackson, Lisa, Mulligan, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158692/
https://www.ncbi.nlm.nih.gov/pubmed/32041104
http://dx.doi.org/10.3390/vaccines8010069
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author Anderson, Evan J.
Lai, Lilin
Wrammert, Jens
Kabbani, Sarah
Xu, Yongxian
Priyamvada, Lalita
Hill, Heather
Goll, Johannes B.
Jensen, Travis L.
Kao, Carol
Yildirim, Inci
Rouphael, Nadine
Jackson, Lisa
Mulligan, Mark J.
author_facet Anderson, Evan J.
Lai, Lilin
Wrammert, Jens
Kabbani, Sarah
Xu, Yongxian
Priyamvada, Lalita
Hill, Heather
Goll, Johannes B.
Jensen, Travis L.
Kao, Carol
Yildirim, Inci
Rouphael, Nadine
Jackson, Lisa
Mulligan, Mark J.
author_sort Anderson, Evan J.
collection PubMed
description Background: Vaccinia is known to induce antibody and cellular responses. Plasmablast, circulating follicular helper T (cT(FH)) cells, cytokine-expressing CD4 T cells, and memory B cells were compared between subcutaneous (SC) and needle-free jet injection (JI) recipients of non-replicating modified vaccinia Ankara (MVA) vaccine. Methods: Vaccinia-naïve adults received MVA SC or by JI on Days 1 and 29. Vaccinia-specific antibodies were quantified by plaque reduction neutralization test (PRNT) and enzyme-linked immunosorbent assay. Plasmablast, cT(FH), and cytokine-expressing CD4 T cells were assessed on Days 1, 8, 15, 29, 36, 43 (cT(FH) and CD4+ only) and 57. Memory B cells were measured on Days 1 and 57. Results: Of the 36 enrolled subjects, only 22 received both vaccinations and had evaluable specimens after the second vaccine. Plasmablasts peaked one week after each vaccine. Day 15 plasmablasts correlated with peak PRNT titers. cT(FH) peaked on Days 8 and 36 and correlated with Day 36 plasmablasts. CD4+ peaked at Day 29 and one-third produced ≥2 cytokines. Day 57 memory B cells ranged from 0.1% to 0.17% of IgG-secreting B cells. Conclusions: This study provides insights into the cellular responses to non-replicating MVA, currently used as a vector for a variety of novel vaccines.
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spelling pubmed-71586922020-04-21 Plasmablast, Memory B Cell, CD4+ T Cell, and Circulating Follicular Helper T Cell Responses to a Non-Replicating Modified Vaccinia Ankara Vaccine Anderson, Evan J. Lai, Lilin Wrammert, Jens Kabbani, Sarah Xu, Yongxian Priyamvada, Lalita Hill, Heather Goll, Johannes B. Jensen, Travis L. Kao, Carol Yildirim, Inci Rouphael, Nadine Jackson, Lisa Mulligan, Mark J. Vaccines (Basel) Article Background: Vaccinia is known to induce antibody and cellular responses. Plasmablast, circulating follicular helper T (cT(FH)) cells, cytokine-expressing CD4 T cells, and memory B cells were compared between subcutaneous (SC) and needle-free jet injection (JI) recipients of non-replicating modified vaccinia Ankara (MVA) vaccine. Methods: Vaccinia-naïve adults received MVA SC or by JI on Days 1 and 29. Vaccinia-specific antibodies were quantified by plaque reduction neutralization test (PRNT) and enzyme-linked immunosorbent assay. Plasmablast, cT(FH), and cytokine-expressing CD4 T cells were assessed on Days 1, 8, 15, 29, 36, 43 (cT(FH) and CD4+ only) and 57. Memory B cells were measured on Days 1 and 57. Results: Of the 36 enrolled subjects, only 22 received both vaccinations and had evaluable specimens after the second vaccine. Plasmablasts peaked one week after each vaccine. Day 15 plasmablasts correlated with peak PRNT titers. cT(FH) peaked on Days 8 and 36 and correlated with Day 36 plasmablasts. CD4+ peaked at Day 29 and one-third produced ≥2 cytokines. Day 57 memory B cells ranged from 0.1% to 0.17% of IgG-secreting B cells. Conclusions: This study provides insights into the cellular responses to non-replicating MVA, currently used as a vector for a variety of novel vaccines. MDPI 2020-02-06 /pmc/articles/PMC7158692/ /pubmed/32041104 http://dx.doi.org/10.3390/vaccines8010069 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Anderson, Evan J.
Lai, Lilin
Wrammert, Jens
Kabbani, Sarah
Xu, Yongxian
Priyamvada, Lalita
Hill, Heather
Goll, Johannes B.
Jensen, Travis L.
Kao, Carol
Yildirim, Inci
Rouphael, Nadine
Jackson, Lisa
Mulligan, Mark J.
Plasmablast, Memory B Cell, CD4+ T Cell, and Circulating Follicular Helper T Cell Responses to a Non-Replicating Modified Vaccinia Ankara Vaccine
title Plasmablast, Memory B Cell, CD4+ T Cell, and Circulating Follicular Helper T Cell Responses to a Non-Replicating Modified Vaccinia Ankara Vaccine
title_full Plasmablast, Memory B Cell, CD4+ T Cell, and Circulating Follicular Helper T Cell Responses to a Non-Replicating Modified Vaccinia Ankara Vaccine
title_fullStr Plasmablast, Memory B Cell, CD4+ T Cell, and Circulating Follicular Helper T Cell Responses to a Non-Replicating Modified Vaccinia Ankara Vaccine
title_full_unstemmed Plasmablast, Memory B Cell, CD4+ T Cell, and Circulating Follicular Helper T Cell Responses to a Non-Replicating Modified Vaccinia Ankara Vaccine
title_short Plasmablast, Memory B Cell, CD4+ T Cell, and Circulating Follicular Helper T Cell Responses to a Non-Replicating Modified Vaccinia Ankara Vaccine
title_sort plasmablast, memory b cell, cd4+ t cell, and circulating follicular helper t cell responses to a non-replicating modified vaccinia ankara vaccine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158692/
https://www.ncbi.nlm.nih.gov/pubmed/32041104
http://dx.doi.org/10.3390/vaccines8010069
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