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SARS-CoV-2 vaccine safety and immunogenicity in patients with hematologic malignancies, transplantation, and cellular therapies
Individuals with hematological malignancies and hematopoietic stem cell transplant (HCT) recipients are immunologically heterogenous groups with varying degrees of immunosuppression at increased risk of severe disease and mortality from SARS-CoV-2 infection. SARS-CoV-2 vaccines are key interventions...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188822/ https://www.ncbi.nlm.nih.gov/pubmed/35752546 http://dx.doi.org/10.1016/j.blre.2022.100984 |
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author | Ni, Bin Yanis, Ahmad Dee, Kevin Chappell, James D. Dulek, Daniel E. Kassim, Adetola A. Kitko, Carrie L. Thomas, Lora D. Halasa, Natasha |
author_facet | Ni, Bin Yanis, Ahmad Dee, Kevin Chappell, James D. Dulek, Daniel E. Kassim, Adetola A. Kitko, Carrie L. Thomas, Lora D. Halasa, Natasha |
author_sort | Ni, Bin |
collection | PubMed |
description | Individuals with hematological malignancies and hematopoietic stem cell transplant (HCT) recipients are immunologically heterogenous groups with varying degrees of immunosuppression at increased risk of severe disease and mortality from SARS-CoV-2 infection. SARS-CoV-2 vaccines are key interventions to preventing severe COVID-19 and its complications. While these individuals were excluded from initial vaccine trials, there is now a growing body of acceptable safety and immunogenicity data among these individuals. A consistent signal for new or worsening graft versus host disease in allogeneic HCT recipients has not been demonstrated post-vaccination. Immunogenicity in these populations is variable depending on disease and treatment factors. However, serological responses may not accurately reflect vaccine protection as correlates of protection within these populations are not yet established. Large-scale studies powered to identify rare serious events, resolve differences in vaccine responses between different vaccination strategies, and identify immune correlates of protection within these populations are needed. |
format | Online Article Text |
id | pubmed-9188822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Authors. Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91888222022-06-13 SARS-CoV-2 vaccine safety and immunogenicity in patients with hematologic malignancies, transplantation, and cellular therapies Ni, Bin Yanis, Ahmad Dee, Kevin Chappell, James D. Dulek, Daniel E. Kassim, Adetola A. Kitko, Carrie L. Thomas, Lora D. Halasa, Natasha Blood Rev Review Individuals with hematological malignancies and hematopoietic stem cell transplant (HCT) recipients are immunologically heterogenous groups with varying degrees of immunosuppression at increased risk of severe disease and mortality from SARS-CoV-2 infection. SARS-CoV-2 vaccines are key interventions to preventing severe COVID-19 and its complications. While these individuals were excluded from initial vaccine trials, there is now a growing body of acceptable safety and immunogenicity data among these individuals. A consistent signal for new or worsening graft versus host disease in allogeneic HCT recipients has not been demonstrated post-vaccination. Immunogenicity in these populations is variable depending on disease and treatment factors. However, serological responses may not accurately reflect vaccine protection as correlates of protection within these populations are not yet established. Large-scale studies powered to identify rare serious events, resolve differences in vaccine responses between different vaccination strategies, and identify immune correlates of protection within these populations are needed. The Authors. Published by Elsevier Ltd. 2022-11 2022-06-12 /pmc/articles/PMC9188822/ /pubmed/35752546 http://dx.doi.org/10.1016/j.blre.2022.100984 Text en © 2022 The Authors 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 | Review Ni, Bin Yanis, Ahmad Dee, Kevin Chappell, James D. Dulek, Daniel E. Kassim, Adetola A. Kitko, Carrie L. Thomas, Lora D. Halasa, Natasha SARS-CoV-2 vaccine safety and immunogenicity in patients with hematologic malignancies, transplantation, and cellular therapies |
title | SARS-CoV-2 vaccine safety and immunogenicity in patients with hematologic malignancies, transplantation, and cellular therapies |
title_full | SARS-CoV-2 vaccine safety and immunogenicity in patients with hematologic malignancies, transplantation, and cellular therapies |
title_fullStr | SARS-CoV-2 vaccine safety and immunogenicity in patients with hematologic malignancies, transplantation, and cellular therapies |
title_full_unstemmed | SARS-CoV-2 vaccine safety and immunogenicity in patients with hematologic malignancies, transplantation, and cellular therapies |
title_short | SARS-CoV-2 vaccine safety and immunogenicity in patients with hematologic malignancies, transplantation, and cellular therapies |
title_sort | sars-cov-2 vaccine safety and immunogenicity in patients with hematologic malignancies, transplantation, and cellular therapies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188822/ https://www.ncbi.nlm.nih.gov/pubmed/35752546 http://dx.doi.org/10.1016/j.blre.2022.100984 |
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