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Immune responses against SARS-CoV-2 variants after two and three doses of vaccine in B-cell malignancies: UK PROSECO study

Patients with hematological malignancies are at increased risk of severe COVID-19 outcomes due to compromised immune responses, but the insights of these studies have been compromised due to intrinsic limitations in study design. Here we present the PROSECO prospective observational study (NCT048585...

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Autores principales: Lim, Sean H., Stuart, Beth, Joseph-Pietras, Debora, Johnson, Marina, Campbell, Nicola, Kelly, Adam, Jeffrey, Danielle, Turaj, Anna H., Rolfvondenbaumen, Kate, Galloway, Celine, Wynn, Thomas, Coleman, Adam R., Ward, Benjamin, Long, Karen, Coleman, Helen, Mundy, Carina, Bates, Andrew T., Ayres, Diana, Lown, Robert, Falconer, Janlyn, Brake, Oliver, Batchelor, James, Willimott, Victoria, Bowzyk Al-Naeeb, Anna, Robinson, Lisa, O’Callaghan, Ann, Collins, Graham P., Menne, Tobias, Faust, Saul N., Fox, Christopher P., Ahearne, Matthew, Johnson, Peter W. M., Davies, Andrew J., Goldblatt, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135622/
https://www.ncbi.nlm.nih.gov/pubmed/35332334
http://dx.doi.org/10.1038/s43018-022-00364-3
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author Lim, Sean H.
Stuart, Beth
Joseph-Pietras, Debora
Johnson, Marina
Campbell, Nicola
Kelly, Adam
Jeffrey, Danielle
Turaj, Anna H.
Rolfvondenbaumen, Kate
Galloway, Celine
Wynn, Thomas
Coleman, Adam R.
Ward, Benjamin
Long, Karen
Coleman, Helen
Mundy, Carina
Bates, Andrew T.
Ayres, Diana
Lown, Robert
Falconer, Janlyn
Brake, Oliver
Batchelor, James
Willimott, Victoria
Bowzyk Al-Naeeb, Anna
Robinson, Lisa
O’Callaghan, Ann
Collins, Graham P.
Menne, Tobias
Faust, Saul N.
Fox, Christopher P.
Ahearne, Matthew
Johnson, Peter W. M.
Davies, Andrew J.
Goldblatt, David
author_facet Lim, Sean H.
Stuart, Beth
Joseph-Pietras, Debora
Johnson, Marina
Campbell, Nicola
Kelly, Adam
Jeffrey, Danielle
Turaj, Anna H.
Rolfvondenbaumen, Kate
Galloway, Celine
Wynn, Thomas
Coleman, Adam R.
Ward, Benjamin
Long, Karen
Coleman, Helen
Mundy, Carina
Bates, Andrew T.
Ayres, Diana
Lown, Robert
Falconer, Janlyn
Brake, Oliver
Batchelor, James
Willimott, Victoria
Bowzyk Al-Naeeb, Anna
Robinson, Lisa
O’Callaghan, Ann
Collins, Graham P.
Menne, Tobias
Faust, Saul N.
Fox, Christopher P.
Ahearne, Matthew
Johnson, Peter W. M.
Davies, Andrew J.
Goldblatt, David
author_sort Lim, Sean H.
collection PubMed
description Patients with hematological malignancies are at increased risk of severe COVID-19 outcomes due to compromised immune responses, but the insights of these studies have been compromised due to intrinsic limitations in study design. Here we present the PROSECO prospective observational study (NCT04858568) on 457 patients with lymphoma that received two or three COVID-19 vaccine doses. We show undetectable humoral responses following two vaccine doses in 52% of patients undergoing active anticancer treatment. Moreover, 60% of patients on anti-CD20 therapy had undetectable antibodies following full vaccination within 12 months of receiving their anticancer therapy. However, 70% of individuals with indolent B-cell lymphoma displayed improved antibody responses following booster vaccination. Notably, 63% of all patients displayed antigen-specific T-cell responses, which increased after a third dose irrespective of their cancer treatment status. Our results emphasize the urgency of careful monitoring of COVID-19-specific immune responses to guide vaccination schemes in these vulnerable populations.
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spelling pubmed-91356222022-05-28 Immune responses against SARS-CoV-2 variants after two and three doses of vaccine in B-cell malignancies: UK PROSECO study Lim, Sean H. Stuart, Beth Joseph-Pietras, Debora Johnson, Marina Campbell, Nicola Kelly, Adam Jeffrey, Danielle Turaj, Anna H. Rolfvondenbaumen, Kate Galloway, Celine Wynn, Thomas Coleman, Adam R. Ward, Benjamin Long, Karen Coleman, Helen Mundy, Carina Bates, Andrew T. Ayres, Diana Lown, Robert Falconer, Janlyn Brake, Oliver Batchelor, James Willimott, Victoria Bowzyk Al-Naeeb, Anna Robinson, Lisa O’Callaghan, Ann Collins, Graham P. Menne, Tobias Faust, Saul N. Fox, Christopher P. Ahearne, Matthew Johnson, Peter W. M. Davies, Andrew J. Goldblatt, David Nat Cancer Article Patients with hematological malignancies are at increased risk of severe COVID-19 outcomes due to compromised immune responses, but the insights of these studies have been compromised due to intrinsic limitations in study design. Here we present the PROSECO prospective observational study (NCT04858568) on 457 patients with lymphoma that received two or three COVID-19 vaccine doses. We show undetectable humoral responses following two vaccine doses in 52% of patients undergoing active anticancer treatment. Moreover, 60% of patients on anti-CD20 therapy had undetectable antibodies following full vaccination within 12 months of receiving their anticancer therapy. However, 70% of individuals with indolent B-cell lymphoma displayed improved antibody responses following booster vaccination. Notably, 63% of all patients displayed antigen-specific T-cell responses, which increased after a third dose irrespective of their cancer treatment status. Our results emphasize the urgency of careful monitoring of COVID-19-specific immune responses to guide vaccination schemes in these vulnerable populations. Nature Publishing Group US 2022-03-24 2022 /pmc/articles/PMC9135622/ /pubmed/35332334 http://dx.doi.org/10.1038/s43018-022-00364-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lim, Sean H.
Stuart, Beth
Joseph-Pietras, Debora
Johnson, Marina
Campbell, Nicola
Kelly, Adam
Jeffrey, Danielle
Turaj, Anna H.
Rolfvondenbaumen, Kate
Galloway, Celine
Wynn, Thomas
Coleman, Adam R.
Ward, Benjamin
Long, Karen
Coleman, Helen
Mundy, Carina
Bates, Andrew T.
Ayres, Diana
Lown, Robert
Falconer, Janlyn
Brake, Oliver
Batchelor, James
Willimott, Victoria
Bowzyk Al-Naeeb, Anna
Robinson, Lisa
O’Callaghan, Ann
Collins, Graham P.
Menne, Tobias
Faust, Saul N.
Fox, Christopher P.
Ahearne, Matthew
Johnson, Peter W. M.
Davies, Andrew J.
Goldblatt, David
Immune responses against SARS-CoV-2 variants after two and three doses of vaccine in B-cell malignancies: UK PROSECO study
title Immune responses against SARS-CoV-2 variants after two and three doses of vaccine in B-cell malignancies: UK PROSECO study
title_full Immune responses against SARS-CoV-2 variants after two and three doses of vaccine in B-cell malignancies: UK PROSECO study
title_fullStr Immune responses against SARS-CoV-2 variants after two and three doses of vaccine in B-cell malignancies: UK PROSECO study
title_full_unstemmed Immune responses against SARS-CoV-2 variants after two and three doses of vaccine in B-cell malignancies: UK PROSECO study
title_short Immune responses against SARS-CoV-2 variants after two and three doses of vaccine in B-cell malignancies: UK PROSECO study
title_sort immune responses against sars-cov-2 variants after two and three doses of vaccine in b-cell malignancies: uk proseco study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135622/
https://www.ncbi.nlm.nih.gov/pubmed/35332334
http://dx.doi.org/10.1038/s43018-022-00364-3
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