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Antibody Response to SARS-CoV-2 Vaccination in Patients following Allogeneic Hematopoietic Cell Transplantation
Vaccines against SARS-CoV-2 have been rapidly approved. Although pivotal studies were conducted in healthy volunteers, little information is available on the safety and efficacy of mRNA vaccines in immunocompromised patients, including recipients of allogeneic hematopoietic cell transplantation (all...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802693/ https://www.ncbi.nlm.nih.gov/pubmed/35092892 http://dx.doi.org/10.1016/j.jtct.2022.01.019 |
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author | Huang, Alice Cicin-Sain, Caroline Pasin, Chloe Epp, Selina Audigé, Annette Müller, Nicolas J. Nilsson, Jakob Bankova, Andriyana Wolfensberger, Nathan Vilinovszki, Oliver Nair, Gayathri Hockl, Philipp Schanz, Urs Kouyos, Roger D. Hasse, Barbara Zinkernagel, Annelies S. Trkola, Alexandra Manz, Markus G. Abela, Irene A. Müller, Antonia M.S. |
author_facet | Huang, Alice Cicin-Sain, Caroline Pasin, Chloe Epp, Selina Audigé, Annette Müller, Nicolas J. Nilsson, Jakob Bankova, Andriyana Wolfensberger, Nathan Vilinovszki, Oliver Nair, Gayathri Hockl, Philipp Schanz, Urs Kouyos, Roger D. Hasse, Barbara Zinkernagel, Annelies S. Trkola, Alexandra Manz, Markus G. Abela, Irene A. Müller, Antonia M.S. |
author_sort | Huang, Alice |
collection | PubMed |
description | Vaccines against SARS-CoV-2 have been rapidly approved. Although pivotal studies were conducted in healthy volunteers, little information is available on the safety and efficacy of mRNA vaccines in immunocompromised patients, including recipients of allogeneic hematopoietic cell transplantation (allo-HCT). Here we used a novel assay to analyze patient- and transplantation-related factors and their influence on immune responses to SARS-CoV-2 vaccination over an extended period (up to 6 months) in a large and homogenous group of allo-HCT recipients at a single center in Switzerland. We examined longitudinal antibody responses to SARS-CoV-2 vaccination with BNT162b2 (BioNTech/Pfizer) and mRNA-1273 (Moderna) in 110 allo-HCT recipients and 86 healthy controls. Seroprofiling recording IgG, IgA, and IgM reactivity against SARS-CoV-2 antigens (receptor-binding domain, spike glycoprotein subunits S1 and S2, and nucleocapsid protein) was performed before vaccination, before the second dose, and at 1, 3, and 6 months after the second dose. Patients were stratified to 3 groups: 3 to 6 months post-allo-HCT, 6 to 12 months post-allo-HCT, and >12 months post-allo-HCT. Patients in the 3 to 6 months and 6 to 12 months post-allo-HCT groups developed significantly lower antibody titers after vaccination compared with patients in the >12 months post-allo-HCT group and healthy controls (P < .001). Within the cohort of allo-HCT recipients, patients age >65 years (P = .030), those receiving immunosuppression for prevention or treatment of graft-versus-host disease (GVHD) (P = .033), and patients with relapsed disease (P = .014) displayed low humoral immune responses to the vaccine. In contrast, the intensity of the conditioning regimen, underlying disease (myeloid/lymphoid/other), and presence of chronic GVHD had no impact on antibody levels. Antibody titers achieved the highest levels at 1 month after the second dose of the vaccine but waned substantially in all transplantation groups and healthy controls over time. This analysis of long-term vaccine antibody response is of critical importance to allo-HCT recipients and transplant physicians to guide treatment decisions regarding revaccination and social behavior during the SARS-CoV-2 pandemic. |
format | Online Article Text |
id | pubmed-8802693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88026932022-01-31 Antibody Response to SARS-CoV-2 Vaccination in Patients following Allogeneic Hematopoietic Cell Transplantation Huang, Alice Cicin-Sain, Caroline Pasin, Chloe Epp, Selina Audigé, Annette Müller, Nicolas J. Nilsson, Jakob Bankova, Andriyana Wolfensberger, Nathan Vilinovszki, Oliver Nair, Gayathri Hockl, Philipp Schanz, Urs Kouyos, Roger D. Hasse, Barbara Zinkernagel, Annelies S. Trkola, Alexandra Manz, Markus G. Abela, Irene A. Müller, Antonia M.S. Transplant Cell Ther Full Length Article Vaccines against SARS-CoV-2 have been rapidly approved. Although pivotal studies were conducted in healthy volunteers, little information is available on the safety and efficacy of mRNA vaccines in immunocompromised patients, including recipients of allogeneic hematopoietic cell transplantation (allo-HCT). Here we used a novel assay to analyze patient- and transplantation-related factors and their influence on immune responses to SARS-CoV-2 vaccination over an extended period (up to 6 months) in a large and homogenous group of allo-HCT recipients at a single center in Switzerland. We examined longitudinal antibody responses to SARS-CoV-2 vaccination with BNT162b2 (BioNTech/Pfizer) and mRNA-1273 (Moderna) in 110 allo-HCT recipients and 86 healthy controls. Seroprofiling recording IgG, IgA, and IgM reactivity against SARS-CoV-2 antigens (receptor-binding domain, spike glycoprotein subunits S1 and S2, and nucleocapsid protein) was performed before vaccination, before the second dose, and at 1, 3, and 6 months after the second dose. Patients were stratified to 3 groups: 3 to 6 months post-allo-HCT, 6 to 12 months post-allo-HCT, and >12 months post-allo-HCT. Patients in the 3 to 6 months and 6 to 12 months post-allo-HCT groups developed significantly lower antibody titers after vaccination compared with patients in the >12 months post-allo-HCT group and healthy controls (P < .001). Within the cohort of allo-HCT recipients, patients age >65 years (P = .030), those receiving immunosuppression for prevention or treatment of graft-versus-host disease (GVHD) (P = .033), and patients with relapsed disease (P = .014) displayed low humoral immune responses to the vaccine. In contrast, the intensity of the conditioning regimen, underlying disease (myeloid/lymphoid/other), and presence of chronic GVHD had no impact on antibody levels. Antibody titers achieved the highest levels at 1 month after the second dose of the vaccine but waned substantially in all transplantation groups and healthy controls over time. This analysis of long-term vaccine antibody response is of critical importance to allo-HCT recipients and transplant physicians to guide treatment decisions regarding revaccination and social behavior during the SARS-CoV-2 pandemic. The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. 2022-04 2022-01-31 /pmc/articles/PMC8802693/ /pubmed/35092892 http://dx.doi.org/10.1016/j.jtct.2022.01.019 Text en © 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Full Length Article Huang, Alice Cicin-Sain, Caroline Pasin, Chloe Epp, Selina Audigé, Annette Müller, Nicolas J. Nilsson, Jakob Bankova, Andriyana Wolfensberger, Nathan Vilinovszki, Oliver Nair, Gayathri Hockl, Philipp Schanz, Urs Kouyos, Roger D. Hasse, Barbara Zinkernagel, Annelies S. Trkola, Alexandra Manz, Markus G. Abela, Irene A. Müller, Antonia M.S. Antibody Response to SARS-CoV-2 Vaccination in Patients following Allogeneic Hematopoietic Cell Transplantation |
title | Antibody Response to SARS-CoV-2 Vaccination in Patients following Allogeneic Hematopoietic Cell Transplantation |
title_full | Antibody Response to SARS-CoV-2 Vaccination in Patients following Allogeneic Hematopoietic Cell Transplantation |
title_fullStr | Antibody Response to SARS-CoV-2 Vaccination in Patients following Allogeneic Hematopoietic Cell Transplantation |
title_full_unstemmed | Antibody Response to SARS-CoV-2 Vaccination in Patients following Allogeneic Hematopoietic Cell Transplantation |
title_short | Antibody Response to SARS-CoV-2 Vaccination in Patients following Allogeneic Hematopoietic Cell Transplantation |
title_sort | antibody response to sars-cov-2 vaccination in patients following allogeneic hematopoietic cell transplantation |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802693/ https://www.ncbi.nlm.nih.gov/pubmed/35092892 http://dx.doi.org/10.1016/j.jtct.2022.01.019 |
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