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T cell immunity following COVID-19 vaccination in adult patients with primary antibody deficiency – a 22-month follow-up

Primary antibody deficiencies, such as common variable immunodeficiency (CVID), are heterogenous disease entities consisting of primary hypogammaglobulinemia and impaired antibody responses to vaccination and natural infection. CVID is the most common primary immunodeficiency in adults, presenting w...

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Autores principales: Hurme, Antti, Jalkanen, Pinja, Marttila-Vaara, Minna, Heroum, Jemna, Jokinen, Heidi, Vara, Saimi, Liedes, Oona, Lempainen, Johanna, Melin, Merit, Julkunen, Ilkka, Kainulainen, Leena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206403/
https://www.ncbi.nlm.nih.gov/pubmed/37234151
http://dx.doi.org/10.3389/fimmu.2023.1146500
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author Hurme, Antti
Jalkanen, Pinja
Marttila-Vaara, Minna
Heroum, Jemna
Jokinen, Heidi
Vara, Saimi
Liedes, Oona
Lempainen, Johanna
Melin, Merit
Julkunen, Ilkka
Kainulainen, Leena
author_facet Hurme, Antti
Jalkanen, Pinja
Marttila-Vaara, Minna
Heroum, Jemna
Jokinen, Heidi
Vara, Saimi
Liedes, Oona
Lempainen, Johanna
Melin, Merit
Julkunen, Ilkka
Kainulainen, Leena
author_sort Hurme, Antti
collection PubMed
description Primary antibody deficiencies, such as common variable immunodeficiency (CVID), are heterogenous disease entities consisting of primary hypogammaglobulinemia and impaired antibody responses to vaccination and natural infection. CVID is the most common primary immunodeficiency in adults, presenting with recurrent bacterial infections, enteropathy, autoimmune disorders, interstitial lung diseases and increased risk of malignancies. Patients with CVID are recommended to be vaccinated against SARS-CoV-2, but there are relatively few studies investigating humoral and cellular responses to immunization. We studied the dynamics of humoral and cell-mediated immunity responses up to 22 months in 28 patients with primary immunodeficiency and three patients with secondary immunodeficiency receiving ChAdOx1, BNT162b2 and mRNA-1273 COVID-19 vaccines. Despite inadequate humoral response to immunization, we demonstrate a robust T cell activation likely protecting from severe COVID-19.
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spelling pubmed-102064032023-05-25 T cell immunity following COVID-19 vaccination in adult patients with primary antibody deficiency – a 22-month follow-up Hurme, Antti Jalkanen, Pinja Marttila-Vaara, Minna Heroum, Jemna Jokinen, Heidi Vara, Saimi Liedes, Oona Lempainen, Johanna Melin, Merit Julkunen, Ilkka Kainulainen, Leena Front Immunol Immunology Primary antibody deficiencies, such as common variable immunodeficiency (CVID), are heterogenous disease entities consisting of primary hypogammaglobulinemia and impaired antibody responses to vaccination and natural infection. CVID is the most common primary immunodeficiency in adults, presenting with recurrent bacterial infections, enteropathy, autoimmune disorders, interstitial lung diseases and increased risk of malignancies. Patients with CVID are recommended to be vaccinated against SARS-CoV-2, but there are relatively few studies investigating humoral and cellular responses to immunization. We studied the dynamics of humoral and cell-mediated immunity responses up to 22 months in 28 patients with primary immunodeficiency and three patients with secondary immunodeficiency receiving ChAdOx1, BNT162b2 and mRNA-1273 COVID-19 vaccines. Despite inadequate humoral response to immunization, we demonstrate a robust T cell activation likely protecting from severe COVID-19. Frontiers Media S.A. 2023-05-09 /pmc/articles/PMC10206403/ /pubmed/37234151 http://dx.doi.org/10.3389/fimmu.2023.1146500 Text en Copyright © 2023 Hurme, Jalkanen, Marttila-Vaara, Heroum, Jokinen, Vara, Liedes, Lempainen, Melin, Julkunen and Kainulainen https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Hurme, Antti
Jalkanen, Pinja
Marttila-Vaara, Minna
Heroum, Jemna
Jokinen, Heidi
Vara, Saimi
Liedes, Oona
Lempainen, Johanna
Melin, Merit
Julkunen, Ilkka
Kainulainen, Leena
T cell immunity following COVID-19 vaccination in adult patients with primary antibody deficiency – a 22-month follow-up
title T cell immunity following COVID-19 vaccination in adult patients with primary antibody deficiency – a 22-month follow-up
title_full T cell immunity following COVID-19 vaccination in adult patients with primary antibody deficiency – a 22-month follow-up
title_fullStr T cell immunity following COVID-19 vaccination in adult patients with primary antibody deficiency – a 22-month follow-up
title_full_unstemmed T cell immunity following COVID-19 vaccination in adult patients with primary antibody deficiency – a 22-month follow-up
title_short T cell immunity following COVID-19 vaccination in adult patients with primary antibody deficiency – a 22-month follow-up
title_sort t cell immunity following covid-19 vaccination in adult patients with primary antibody deficiency – a 22-month follow-up
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206403/
https://www.ncbi.nlm.nih.gov/pubmed/37234151
http://dx.doi.org/10.3389/fimmu.2023.1146500
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