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Prospective Evaluation of Coronavirus Disease 2019 (COVID-19) Vaccine Responses Across a Broad Spectrum of Immunocompromising Conditions: the COVID-19 Vaccination in the Immunocompromised Study (COVICS)

BACKGROUND: We studied humoral responses after coronavirus disease 2019 (COVID-19) vaccination across varying causes of immunodeficiency. METHODS: Prospective study of fully vaccinated immunocompromised adults (solid organ transplant [SOT], hematologic malignancy, solid cancers, autoimmune condition...

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Autores principales: Haidar, Ghady, Agha, Mounzer, Bilderback, Andrew, Lukanski, Amy, Linstrum, Kelsey, Troyan, Rachel, Rothenberger, Scott, McMahon, Deborah K, Crandall, Melissa D, Sobolewksi, Michele D, Nathan Enick, P, Jacobs, Jana L, Collins, Kevin, Klamar-Blain, Cynthia, Macatangay, Bernard J C, Parikh, Urvi M, Heaps, Amy, Coughenour, Lindsay, Schwartz, Marc B, Dueker, Jeffrey M, Silveira, Fernanda P, Keebler, Mary E, Humar, Abhinav, Luketich, James D, Morrell, Matthew R, Pilewski, Joseph M, McDyer, John F, Pappu, Bhanu, Ferris, Robert L, Marks, Stanley M, Mahon, John, Mulvey, Katie, Hariharan, Sundaram, Updike, Glenn M, Brock, Lorraine, Edwards, Robert, Beigi, Richard H, Kip, Paula L, Wells, Alan, Minnier, Tami, Angus, Derek C, Mellors, John W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903515/
https://www.ncbi.nlm.nih.gov/pubmed/35179197
http://dx.doi.org/10.1093/cid/ciac103
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author Haidar, Ghady
Agha, Mounzer
Bilderback, Andrew
Lukanski, Amy
Linstrum, Kelsey
Troyan, Rachel
Rothenberger, Scott
McMahon, Deborah K
Crandall, Melissa D
Sobolewksi, Michele D
Nathan Enick, P
Jacobs, Jana L
Collins, Kevin
Klamar-Blain, Cynthia
Macatangay, Bernard J C
Parikh, Urvi M
Heaps, Amy
Coughenour, Lindsay
Schwartz, Marc B
Dueker, Jeffrey M
Silveira, Fernanda P
Keebler, Mary E
Humar, Abhinav
Luketich, James D
Morrell, Matthew R
Pilewski, Joseph M
McDyer, John F
Pappu, Bhanu
Ferris, Robert L
Marks, Stanley M
Mahon, John
Mulvey, Katie
Hariharan, Sundaram
Updike, Glenn M
Brock, Lorraine
Edwards, Robert
Beigi, Richard H
Kip, Paula L
Wells, Alan
Minnier, Tami
Angus, Derek C
Mellors, John W
author_facet Haidar, Ghady
Agha, Mounzer
Bilderback, Andrew
Lukanski, Amy
Linstrum, Kelsey
Troyan, Rachel
Rothenberger, Scott
McMahon, Deborah K
Crandall, Melissa D
Sobolewksi, Michele D
Nathan Enick, P
Jacobs, Jana L
Collins, Kevin
Klamar-Blain, Cynthia
Macatangay, Bernard J C
Parikh, Urvi M
Heaps, Amy
Coughenour, Lindsay
Schwartz, Marc B
Dueker, Jeffrey M
Silveira, Fernanda P
Keebler, Mary E
Humar, Abhinav
Luketich, James D
Morrell, Matthew R
Pilewski, Joseph M
McDyer, John F
Pappu, Bhanu
Ferris, Robert L
Marks, Stanley M
Mahon, John
Mulvey, Katie
Hariharan, Sundaram
Updike, Glenn M
Brock, Lorraine
Edwards, Robert
Beigi, Richard H
Kip, Paula L
Wells, Alan
Minnier, Tami
Angus, Derek C
Mellors, John W
author_sort Haidar, Ghady
collection PubMed
description BACKGROUND: We studied humoral responses after coronavirus disease 2019 (COVID-19) vaccination across varying causes of immunodeficiency. METHODS: Prospective study of fully vaccinated immunocompromised adults (solid organ transplant [SOT], hematologic malignancy, solid cancers, autoimmune conditions, human immunodeficiency virus [HIV]) versus nonimmunocompromised healthcare workers (HCWs). The primary outcome was the proportion with a reactive test (seropositive) for immunoglobulin G to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) receptor-binding domain. Secondary outcomes were comparisons of antibody levels and their correlation with pseudovirus neutralization titers. Stepwise logistic regression was used to identify factors associated with seropositivity. RESULTS: A total of 1271 participants enrolled: 1099 immunocompromised and 172 HCW. Compared with HCW (92.4% seropositive), seropositivity was lower among participants with SOT (30.7%), hematological malignancies (50.0%), autoimmune conditions (79.1%), solid tumors (78.7%), and HIV (79.8%) (P < .01). Factors associated with poor seropositivity included age, greater immunosuppression, time since vaccination, anti-CD20 monoclonal antibodies, and vaccination with BNT162b2 (Pfizer) or adenovirus vector vaccines versus messenger RNA (mRNA)-1273 (Moderna). mRNA-1273 was associated with higher antibody levels than BNT162b2 or adenovirus vector vaccines after adjusting for time since vaccination, age, and underlying condition. Antibody levels were strongly correlated with pseudovirus neutralization titers (Spearman r = 0.89, P < .0001), but in seropositive participants with intermediate antibody levels, neutralization titers were significantly lower in immunocompromised individuals versus HCW. CONCLUSIONS: Antibody responses to COVID-19 vaccines were lowest among SOT and anti-CD20 monoclonal recipients, and recipients of vaccines other than mRNA-1273. Among those with intermediate antibody levels, pseudovirus neutralization titers were lower in immunocompromised patients than HCWs. Additional SARS-CoV-2 preventive approaches are needed for immunocompromised persons, which may need to be tailored to the cause of immunodeficiency.
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spelling pubmed-89035152022-03-09 Prospective Evaluation of Coronavirus Disease 2019 (COVID-19) Vaccine Responses Across a Broad Spectrum of Immunocompromising Conditions: the COVID-19 Vaccination in the Immunocompromised Study (COVICS) Haidar, Ghady Agha, Mounzer Bilderback, Andrew Lukanski, Amy Linstrum, Kelsey Troyan, Rachel Rothenberger, Scott McMahon, Deborah K Crandall, Melissa D Sobolewksi, Michele D Nathan Enick, P Jacobs, Jana L Collins, Kevin Klamar-Blain, Cynthia Macatangay, Bernard J C Parikh, Urvi M Heaps, Amy Coughenour, Lindsay Schwartz, Marc B Dueker, Jeffrey M Silveira, Fernanda P Keebler, Mary E Humar, Abhinav Luketich, James D Morrell, Matthew R Pilewski, Joseph M McDyer, John F Pappu, Bhanu Ferris, Robert L Marks, Stanley M Mahon, John Mulvey, Katie Hariharan, Sundaram Updike, Glenn M Brock, Lorraine Edwards, Robert Beigi, Richard H Kip, Paula L Wells, Alan Minnier, Tami Angus, Derek C Mellors, John W Clin Infect Dis Major Article BACKGROUND: We studied humoral responses after coronavirus disease 2019 (COVID-19) vaccination across varying causes of immunodeficiency. METHODS: Prospective study of fully vaccinated immunocompromised adults (solid organ transplant [SOT], hematologic malignancy, solid cancers, autoimmune conditions, human immunodeficiency virus [HIV]) versus nonimmunocompromised healthcare workers (HCWs). The primary outcome was the proportion with a reactive test (seropositive) for immunoglobulin G to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) receptor-binding domain. Secondary outcomes were comparisons of antibody levels and their correlation with pseudovirus neutralization titers. Stepwise logistic regression was used to identify factors associated with seropositivity. RESULTS: A total of 1271 participants enrolled: 1099 immunocompromised and 172 HCW. Compared with HCW (92.4% seropositive), seropositivity was lower among participants with SOT (30.7%), hematological malignancies (50.0%), autoimmune conditions (79.1%), solid tumors (78.7%), and HIV (79.8%) (P < .01). Factors associated with poor seropositivity included age, greater immunosuppression, time since vaccination, anti-CD20 monoclonal antibodies, and vaccination with BNT162b2 (Pfizer) or adenovirus vector vaccines versus messenger RNA (mRNA)-1273 (Moderna). mRNA-1273 was associated with higher antibody levels than BNT162b2 or adenovirus vector vaccines after adjusting for time since vaccination, age, and underlying condition. Antibody levels were strongly correlated with pseudovirus neutralization titers (Spearman r = 0.89, P < .0001), but in seropositive participants with intermediate antibody levels, neutralization titers were significantly lower in immunocompromised individuals versus HCW. CONCLUSIONS: Antibody responses to COVID-19 vaccines were lowest among SOT and anti-CD20 monoclonal recipients, and recipients of vaccines other than mRNA-1273. Among those with intermediate antibody levels, pseudovirus neutralization titers were lower in immunocompromised patients than HCWs. Additional SARS-CoV-2 preventive approaches are needed for immunocompromised persons, which may need to be tailored to the cause of immunodeficiency. Oxford University Press 2022-02-18 /pmc/articles/PMC8903515/ /pubmed/35179197 http://dx.doi.org/10.1093/cid/ciac103 Text en © The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_modelThis article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)
spellingShingle Major Article
Haidar, Ghady
Agha, Mounzer
Bilderback, Andrew
Lukanski, Amy
Linstrum, Kelsey
Troyan, Rachel
Rothenberger, Scott
McMahon, Deborah K
Crandall, Melissa D
Sobolewksi, Michele D
Nathan Enick, P
Jacobs, Jana L
Collins, Kevin
Klamar-Blain, Cynthia
Macatangay, Bernard J C
Parikh, Urvi M
Heaps, Amy
Coughenour, Lindsay
Schwartz, Marc B
Dueker, Jeffrey M
Silveira, Fernanda P
Keebler, Mary E
Humar, Abhinav
Luketich, James D
Morrell, Matthew R
Pilewski, Joseph M
McDyer, John F
Pappu, Bhanu
Ferris, Robert L
Marks, Stanley M
Mahon, John
Mulvey, Katie
Hariharan, Sundaram
Updike, Glenn M
Brock, Lorraine
Edwards, Robert
Beigi, Richard H
Kip, Paula L
Wells, Alan
Minnier, Tami
Angus, Derek C
Mellors, John W
Prospective Evaluation of Coronavirus Disease 2019 (COVID-19) Vaccine Responses Across a Broad Spectrum of Immunocompromising Conditions: the COVID-19 Vaccination in the Immunocompromised Study (COVICS)
title Prospective Evaluation of Coronavirus Disease 2019 (COVID-19) Vaccine Responses Across a Broad Spectrum of Immunocompromising Conditions: the COVID-19 Vaccination in the Immunocompromised Study (COVICS)
title_full Prospective Evaluation of Coronavirus Disease 2019 (COVID-19) Vaccine Responses Across a Broad Spectrum of Immunocompromising Conditions: the COVID-19 Vaccination in the Immunocompromised Study (COVICS)
title_fullStr Prospective Evaluation of Coronavirus Disease 2019 (COVID-19) Vaccine Responses Across a Broad Spectrum of Immunocompromising Conditions: the COVID-19 Vaccination in the Immunocompromised Study (COVICS)
title_full_unstemmed Prospective Evaluation of Coronavirus Disease 2019 (COVID-19) Vaccine Responses Across a Broad Spectrum of Immunocompromising Conditions: the COVID-19 Vaccination in the Immunocompromised Study (COVICS)
title_short Prospective Evaluation of Coronavirus Disease 2019 (COVID-19) Vaccine Responses Across a Broad Spectrum of Immunocompromising Conditions: the COVID-19 Vaccination in the Immunocompromised Study (COVICS)
title_sort prospective evaluation of coronavirus disease 2019 (covid-19) vaccine responses across a broad spectrum of immunocompromising conditions: the covid-19 vaccination in the immunocompromised study (covics)
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903515/
https://www.ncbi.nlm.nih.gov/pubmed/35179197
http://dx.doi.org/10.1093/cid/ciac103
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