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Augmented humoral and cellular immunity against severe acute respiratory syndrome coronavirus 2 after breakthrough infection in kidney transplant recipients who received 3 doses of coronavirus disease 2019 vaccine
Diminished immune response to coronavirus disease 2019 (COVID-19) vaccines and breakthrough infection (BI) is a major concern for solid organ transplant recipients. Humoral and cellular immune responses of kidney transplant (KT) recipients after a third COVID-19 vaccination were investigated compare...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc. on behalf of American Society of Transplantation & American Society of Transplant Surgeons.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807455/ https://www.ncbi.nlm.nih.gov/pubmed/36739177 http://dx.doi.org/10.1016/j.ajt.2022.12.022 |
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author | Yang, Jinyoung Lee, Kyo Won Baek, Jin Yang Bae, Seongman Lee, Young Ho Kim, Haein Huh, Kyungmin Cho, Sun Young Kang, Cheol-In Chung, Doo Ryeon Peck, Kyong Ran Park, Jae Berm Kim, Sung-Han Kim, Tae-Jong Kim, Dong-Min Ko, Jae-Hoon |
author_facet | Yang, Jinyoung Lee, Kyo Won Baek, Jin Yang Bae, Seongman Lee, Young Ho Kim, Haein Huh, Kyungmin Cho, Sun Young Kang, Cheol-In Chung, Doo Ryeon Peck, Kyong Ran Park, Jae Berm Kim, Sung-Han Kim, Tae-Jong Kim, Dong-Min Ko, Jae-Hoon |
author_sort | Yang, Jinyoung |
collection | PubMed |
description | Diminished immune response to coronavirus disease 2019 (COVID-19) vaccines and breakthrough infection (BI) is a major concern for solid organ transplant recipients. Humoral and cellular immune responses of kidney transplant (KT) recipients after a third COVID-19 vaccination were investigated compared to matched health care workers. Anti–severe acute respiratory syndrome coronavirus 2 spike protein antibody and severe acute respiratory syndrome coronavirus 2 specific interferon-gamma releasing assay (IGRA) were assessed. A total of 38 KT recipients, including 20 BI and 18 noninfection, were evaluated. In the KT BI group, antibody titers were significantly increased (median 5 to 724, binding antibody units/mL (P = 0.002) after the third vaccination, but IGRA responses were negligible. After BI, antibody titers increased (median 11 355 binding antibody unit/mL; P < 0.001) and there was a significant increase of IGRA responses to spike proteins (Spike(1)-Nil, median 0.05 to 0.41 IU/mL; P = 0.009). Antibody titers and IGRA responses were significantly higher in the BI than in the noninfection group after 6 months. Immune responses were stronger in the health care worker than in the KT cohort, but the gap became narrower after BI. In conclusion, KT recipients who experienced BI after 3 COVID-19 vaccinations acquired augmented humoral and cellular immune responses. |
format | Online Article Text |
id | pubmed-9807455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Published by Elsevier Inc. on behalf of American Society of Transplantation & American Society of Transplant Surgeons. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98074552023-01-04 Augmented humoral and cellular immunity against severe acute respiratory syndrome coronavirus 2 after breakthrough infection in kidney transplant recipients who received 3 doses of coronavirus disease 2019 vaccine Yang, Jinyoung Lee, Kyo Won Baek, Jin Yang Bae, Seongman Lee, Young Ho Kim, Haein Huh, Kyungmin Cho, Sun Young Kang, Cheol-In Chung, Doo Ryeon Peck, Kyong Ran Park, Jae Berm Kim, Sung-Han Kim, Tae-Jong Kim, Dong-Min Ko, Jae-Hoon Am J Transplant Brief Communication Diminished immune response to coronavirus disease 2019 (COVID-19) vaccines and breakthrough infection (BI) is a major concern for solid organ transplant recipients. Humoral and cellular immune responses of kidney transplant (KT) recipients after a third COVID-19 vaccination were investigated compared to matched health care workers. Anti–severe acute respiratory syndrome coronavirus 2 spike protein antibody and severe acute respiratory syndrome coronavirus 2 specific interferon-gamma releasing assay (IGRA) were assessed. A total of 38 KT recipients, including 20 BI and 18 noninfection, were evaluated. In the KT BI group, antibody titers were significantly increased (median 5 to 724, binding antibody units/mL (P = 0.002) after the third vaccination, but IGRA responses were negligible. After BI, antibody titers increased (median 11 355 binding antibody unit/mL; P < 0.001) and there was a significant increase of IGRA responses to spike proteins (Spike(1)-Nil, median 0.05 to 0.41 IU/mL; P = 0.009). Antibody titers and IGRA responses were significantly higher in the BI than in the noninfection group after 6 months. Immune responses were stronger in the health care worker than in the KT cohort, but the gap became narrower after BI. In conclusion, KT recipients who experienced BI after 3 COVID-19 vaccinations acquired augmented humoral and cellular immune responses. Published by Elsevier Inc. on behalf of American Society of Transplantation & American Society of Transplant Surgeons. 2023-04 2023-01-03 /pmc/articles/PMC9807455/ /pubmed/36739177 http://dx.doi.org/10.1016/j.ajt.2022.12.022 Text en © 2022 Published by Elsevier Inc. on behalf of American Society of Transplantation & American Society of Transplant Surgeons. 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 Communication Yang, Jinyoung Lee, Kyo Won Baek, Jin Yang Bae, Seongman Lee, Young Ho Kim, Haein Huh, Kyungmin Cho, Sun Young Kang, Cheol-In Chung, Doo Ryeon Peck, Kyong Ran Park, Jae Berm Kim, Sung-Han Kim, Tae-Jong Kim, Dong-Min Ko, Jae-Hoon Augmented humoral and cellular immunity against severe acute respiratory syndrome coronavirus 2 after breakthrough infection in kidney transplant recipients who received 3 doses of coronavirus disease 2019 vaccine |
title | Augmented humoral and cellular immunity against severe acute respiratory syndrome coronavirus 2 after breakthrough infection in kidney transplant recipients who received 3 doses of coronavirus disease 2019 vaccine |
title_full | Augmented humoral and cellular immunity against severe acute respiratory syndrome coronavirus 2 after breakthrough infection in kidney transplant recipients who received 3 doses of coronavirus disease 2019 vaccine |
title_fullStr | Augmented humoral and cellular immunity against severe acute respiratory syndrome coronavirus 2 after breakthrough infection in kidney transplant recipients who received 3 doses of coronavirus disease 2019 vaccine |
title_full_unstemmed | Augmented humoral and cellular immunity against severe acute respiratory syndrome coronavirus 2 after breakthrough infection in kidney transplant recipients who received 3 doses of coronavirus disease 2019 vaccine |
title_short | Augmented humoral and cellular immunity against severe acute respiratory syndrome coronavirus 2 after breakthrough infection in kidney transplant recipients who received 3 doses of coronavirus disease 2019 vaccine |
title_sort | augmented humoral and cellular immunity against severe acute respiratory syndrome coronavirus 2 after breakthrough infection in kidney transplant recipients who received 3 doses of coronavirus disease 2019 vaccine |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807455/ https://www.ncbi.nlm.nih.gov/pubmed/36739177 http://dx.doi.org/10.1016/j.ajt.2022.12.022 |
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