Immunity after COVID-19 Recovery and Vaccination: Similarities and Differences

The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is associated with a robust immune response. The development of systemic inflammation leads to a hyperinflammatory state due to cytokine release syndrome during severe COVID-19....

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Main Authors: Dorota Kamińska, Dominika Dęborska-Materkowska, Katarzyna Kościelska-Kasprzak, Oktawia Mazanowska, Agata Remiorz, Paweł Poznański, Magdalena Durlik, Magdalena Krajewska
Format: Article
Language:English
Published: MDPI AG 2022-07-01
Series:Vaccines
Subjects:
Online Access:https://www.mdpi.com/2076-393X/10/7/1068
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author Dorota Kamińska
Dominika Dęborska-Materkowska
Katarzyna Kościelska-Kasprzak
Oktawia Mazanowska
Agata Remiorz
Paweł Poznański
Magdalena Durlik
Magdalena Krajewska
author_facet Dorota Kamińska
Dominika Dęborska-Materkowska
Katarzyna Kościelska-Kasprzak
Oktawia Mazanowska
Agata Remiorz
Paweł Poznański
Magdalena Durlik
Magdalena Krajewska
author_sort Dorota Kamińska
collection DOAJ
description The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is associated with a robust immune response. The development of systemic inflammation leads to a hyperinflammatory state due to cytokine release syndrome during severe COVID-19. The emergence of many new SARS-CoV-2 variants across the world deteriorates the protective antiviral immunity induced after infection or vaccination. The innate immune response to SARS-CoV-2 is crucial for determining the fate of COVID-19 symptomatology. T cell-mediated immunity is the main factor of the antiviral immune response; moreover, SARS-CoV-2 infection initiates a rapid B-cell response. In this paper, we present the current state of knowledge on immunity after COVID-19 infection and vaccination. We discuss the mechanisms of immune response to various types of vaccines (nucleoside-modified, adenovirus-vectored, inactivated virus vaccines and recombinant protein adjuvanted formulations). This includes specific aspects of vaccination in selected patient populations with altered immune activity (the elderly, children, pregnant women, solid organ transplant recipients, patients with systemic rheumatic diseases or malignancies). We also present diagnostic and research tools available to study the anti-SARS-CoV-2 cellular and humoral immune responses.
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spelling doaj.art-3cae1374614b423b805aec3df65ffb272023-12-03T12:22:26ZengMDPI AGVaccines2076-393X2022-07-01107106810.3390/vaccines10071068Immunity after COVID-19 Recovery and Vaccination: Similarities and DifferencesDorota Kamińska0Dominika Dęborska-Materkowska1Katarzyna Kościelska-Kasprzak2Oktawia Mazanowska3Agata Remiorz4Paweł Poznański5Magdalena Durlik6Magdalena Krajewska7Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, PolandDepartment of Transplantation Medicine, Nephrology and Internal Diseases, Medical University of Warsaw, Nowogrodzka 59, 02-006 Warsaw, PolandDepartment of Nephrology and Transplantation Medicine, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, PolandDepartment of Nephrology and Transplantation Medicine, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, PolandDepartment of Nephrology and Transplantation Medicine, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, PolandDepartment of Nephrology and Transplantation Medicine, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, PolandDepartment of Transplantation Medicine, Nephrology and Internal Diseases, Medical University of Warsaw, Nowogrodzka 59, 02-006 Warsaw, PolandDepartment of Nephrology and Transplantation Medicine, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, PolandThe coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is associated with a robust immune response. The development of systemic inflammation leads to a hyperinflammatory state due to cytokine release syndrome during severe COVID-19. The emergence of many new SARS-CoV-2 variants across the world deteriorates the protective antiviral immunity induced after infection or vaccination. The innate immune response to SARS-CoV-2 is crucial for determining the fate of COVID-19 symptomatology. T cell-mediated immunity is the main factor of the antiviral immune response; moreover, SARS-CoV-2 infection initiates a rapid B-cell response. In this paper, we present the current state of knowledge on immunity after COVID-19 infection and vaccination. We discuss the mechanisms of immune response to various types of vaccines (nucleoside-modified, adenovirus-vectored, inactivated virus vaccines and recombinant protein adjuvanted formulations). This includes specific aspects of vaccination in selected patient populations with altered immune activity (the elderly, children, pregnant women, solid organ transplant recipients, patients with systemic rheumatic diseases or malignancies). We also present diagnostic and research tools available to study the anti-SARS-CoV-2 cellular and humoral immune responses.https://www.mdpi.com/2076-393X/10/7/1068COVID-19vaccineimmune response
spellingShingle Dorota Kamińska
Dominika Dęborska-Materkowska
Katarzyna Kościelska-Kasprzak
Oktawia Mazanowska
Agata Remiorz
Paweł Poznański
Magdalena Durlik
Magdalena Krajewska
Immunity after COVID-19 Recovery and Vaccination: Similarities and Differences
Vaccines
COVID-19
vaccine
immune response
title Immunity after COVID-19 Recovery and Vaccination: Similarities and Differences
title_full Immunity after COVID-19 Recovery and Vaccination: Similarities and Differences
title_fullStr Immunity after COVID-19 Recovery and Vaccination: Similarities and Differences
title_full_unstemmed Immunity after COVID-19 Recovery and Vaccination: Similarities and Differences
title_short Immunity after COVID-19 Recovery and Vaccination: Similarities and Differences
title_sort immunity after covid 19 recovery and vaccination similarities and differences
topic COVID-19
vaccine
immune response
url https://www.mdpi.com/2076-393X/10/7/1068
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AT oktawiamazanowska immunityaftercovid19recoveryandvaccinationsimilaritiesanddifferences
AT agataremiorz immunityaftercovid19recoveryandvaccinationsimilaritiesanddifferences
AT pawełpoznanski immunityaftercovid19recoveryandvaccinationsimilaritiesanddifferences
AT magdalenadurlik immunityaftercovid19recoveryandvaccinationsimilaritiesanddifferences
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