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SARS-COV-2 antibodies after booster vaccination. Identification of subgroups with poor response
OBJECTIVE: To determine which patients within the high-risk group are most likely to have insufficient post-vaccination immunity. METHODS: Determination of IgG titers against SARS-CoV-2 after the booster dose. Vaccine response was categorized as negative (IgG titers < 34 BAU/ml), indeterminate (t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Espana
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154241/ https://www.ncbi.nlm.nih.gov/pubmed/37146747 http://dx.doi.org/10.1016/j.rceng.2023.04.008 |
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author | Ayuso García, B. Romay Lema, E. Pérez López, A. Suárez Piñera, A. Pereiro Belay, M.C. Gude González, M.J. Rabuñal Rey, R. |
author_facet | Ayuso García, B. Romay Lema, E. Pérez López, A. Suárez Piñera, A. Pereiro Belay, M.C. Gude González, M.J. Rabuñal Rey, R. |
author_sort | Ayuso García, B. |
collection | PubMed |
description | OBJECTIVE: To determine which patients within the high-risk group are most likely to have insufficient post-vaccination immunity. METHODS: Determination of IgG titers against SARS-CoV-2 after the booster dose. Vaccine response was categorized as negative (IgG titers < 34 BAU/ml), indeterminate (titers 34–259 BAU/ml) or positive (≥260 BAU/ml). RESULTS: 765 patients were included (31.25% of those vaccinated). 54 (7.1%) on treatment with biologics, 90 (11.8%) with hematologic disease, 299 (39.1%) with oncologic pathology, 304 (39.7%) with solid organ transplant and 18 (2.4%) with immunosuppression for other reasons. 74 patients (9.7%) had negative serology and 45 (5.9%) had indeterminate titers. By diagnostic group, the patients with the highest proportion of negative or indeterminate serology were patients with biologic treatment (55.6%, mainly at expense of antiCD20), hematologic (35.4%) and transplant patients (17.8%, mainly lung and kidney). Oncology and other immunosuppressed patients had a favorable response to vaccination. CONCLUSION: Patients treated with antiCD20 drugs, hematologic patients and transplanted patients (mainly lung and kidney) have a higher risk of not achieving post-vaccination immunity. It is essential to identify them in order to individualize and optimize their management. |
format | Online Article Text |
id | pubmed-10154241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier Espana |
record_format | MEDLINE/PubMed |
spelling | pubmed-101542412023-05-03 SARS-COV-2 antibodies after booster vaccination. Identification of subgroups with poor response Ayuso García, B. Romay Lema, E. Pérez López, A. Suárez Piñera, A. Pereiro Belay, M.C. Gude González, M.J. Rabuñal Rey, R. Rev Clin Esp (Barc) Brief Original OBJECTIVE: To determine which patients within the high-risk group are most likely to have insufficient post-vaccination immunity. METHODS: Determination of IgG titers against SARS-CoV-2 after the booster dose. Vaccine response was categorized as negative (IgG titers < 34 BAU/ml), indeterminate (titers 34–259 BAU/ml) or positive (≥260 BAU/ml). RESULTS: 765 patients were included (31.25% of those vaccinated). 54 (7.1%) on treatment with biologics, 90 (11.8%) with hematologic disease, 299 (39.1%) with oncologic pathology, 304 (39.7%) with solid organ transplant and 18 (2.4%) with immunosuppression for other reasons. 74 patients (9.7%) had negative serology and 45 (5.9%) had indeterminate titers. By diagnostic group, the patients with the highest proportion of negative or indeterminate serology were patients with biologic treatment (55.6%, mainly at expense of antiCD20), hematologic (35.4%) and transplant patients (17.8%, mainly lung and kidney). Oncology and other immunosuppressed patients had a favorable response to vaccination. CONCLUSION: Patients treated with antiCD20 drugs, hematologic patients and transplanted patients (mainly lung and kidney) have a higher risk of not achieving post-vaccination immunity. It is essential to identify them in order to individualize and optimize their management. Elsevier Espana 2023 2023-05-03 /pmc/articles/PMC10154241/ /pubmed/37146747 http://dx.doi.org/10.1016/j.rceng.2023.04.008 Text en 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 | Brief Original Ayuso García, B. Romay Lema, E. Pérez López, A. Suárez Piñera, A. Pereiro Belay, M.C. Gude González, M.J. Rabuñal Rey, R. SARS-COV-2 antibodies after booster vaccination. Identification of subgroups with poor response |
title | SARS-COV-2 antibodies after booster vaccination. Identification of subgroups with poor response |
title_full | SARS-COV-2 antibodies after booster vaccination. Identification of subgroups with poor response |
title_fullStr | SARS-COV-2 antibodies after booster vaccination. Identification of subgroups with poor response |
title_full_unstemmed | SARS-COV-2 antibodies after booster vaccination. Identification of subgroups with poor response |
title_short | SARS-COV-2 antibodies after booster vaccination. Identification of subgroups with poor response |
title_sort | sars-cov-2 antibodies after booster vaccination. identification of subgroups with poor response |
topic | Brief Original |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154241/ https://www.ncbi.nlm.nih.gov/pubmed/37146747 http://dx.doi.org/10.1016/j.rceng.2023.04.008 |
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