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Humoral and Cellular Vaccination Responses against SARS-CoV-2 in Hematopoietic Stem Cell Transplant Recipients

The cellular response to SARS-CoV-2 vaccination and infection in allogeneic hematopoietic stem cell transplant (HSCT) recipients is not yet clear. In the current study, HSCT recipients prior to and post vaccination were tested for SARS-CoV-2-specific humoral and cellular immunity. Antibodies against...

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Autores principales: Lindemann, Monika, Klisanin, Vesna, Thümmler, Laura, Fisenkci, Neslinur, Tsachakis-Mück, Nikolaos, Ditschkowski, Markus, Schwarzkopf, Sina, Klump, Hannes, Reinhardt, Hans Christian, Horn, Peter A., Koldehoff, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537291/
https://www.ncbi.nlm.nih.gov/pubmed/34696183
http://dx.doi.org/10.3390/vaccines9101075
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author Lindemann, Monika
Klisanin, Vesna
Thümmler, Laura
Fisenkci, Neslinur
Tsachakis-Mück, Nikolaos
Ditschkowski, Markus
Schwarzkopf, Sina
Klump, Hannes
Reinhardt, Hans Christian
Horn, Peter A.
Koldehoff, Michael
author_facet Lindemann, Monika
Klisanin, Vesna
Thümmler, Laura
Fisenkci, Neslinur
Tsachakis-Mück, Nikolaos
Ditschkowski, Markus
Schwarzkopf, Sina
Klump, Hannes
Reinhardt, Hans Christian
Horn, Peter A.
Koldehoff, Michael
author_sort Lindemann, Monika
collection PubMed
description The cellular response to SARS-CoV-2 vaccination and infection in allogeneic hematopoietic stem cell transplant (HSCT) recipients is not yet clear. In the current study, HSCT recipients prior to and post vaccination were tested for SARS-CoV-2-specific humoral and cellular immunity. Antibodies against spike (S) 1 were assessed by Anti-SARS-CoV-2 IgG ELISA (Euroimmun). Cellular immunity was analyzed by an in house interferon-gamma ELISpot and T-SPOT.COVID (Oxford Immunotec), using altogether seven SARS-CoV-2-specific antigens. In 117 HSCT patients vaccinated twice, SARS-CoV-2 IgG antibodies were significantly higher than in HSCT controls pre vaccination (p < 0.0001). After the second vaccination, we observed a median antibody ratio of 4.7 and 68% positive results, whereas 35 healthy controls reached a median ratio of 9.0 and 100% positivity. ELISpot responses in patients were significantly (p < 0.001) reduced to ≤33% of the controls. After the second vaccination, female HSCT patients and female healthy controls showed significantly higher antibody responses than males (6.0 vs. 2.1 and 9.2 vs. 8.2, respectively; p < 0.05). Cellular immunity was diminished in patients irrespective of sex. In conclusion, especially male HSCT recipients showed impaired antibody responses after SARS-CoV-2 vaccination. Changing the vaccine schedule or composition could help increase vaccine responses.
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spelling pubmed-85372912021-10-24 Humoral and Cellular Vaccination Responses against SARS-CoV-2 in Hematopoietic Stem Cell Transplant Recipients Lindemann, Monika Klisanin, Vesna Thümmler, Laura Fisenkci, Neslinur Tsachakis-Mück, Nikolaos Ditschkowski, Markus Schwarzkopf, Sina Klump, Hannes Reinhardt, Hans Christian Horn, Peter A. Koldehoff, Michael Vaccines (Basel) Article The cellular response to SARS-CoV-2 vaccination and infection in allogeneic hematopoietic stem cell transplant (HSCT) recipients is not yet clear. In the current study, HSCT recipients prior to and post vaccination were tested for SARS-CoV-2-specific humoral and cellular immunity. Antibodies against spike (S) 1 were assessed by Anti-SARS-CoV-2 IgG ELISA (Euroimmun). Cellular immunity was analyzed by an in house interferon-gamma ELISpot and T-SPOT.COVID (Oxford Immunotec), using altogether seven SARS-CoV-2-specific antigens. In 117 HSCT patients vaccinated twice, SARS-CoV-2 IgG antibodies were significantly higher than in HSCT controls pre vaccination (p < 0.0001). After the second vaccination, we observed a median antibody ratio of 4.7 and 68% positive results, whereas 35 healthy controls reached a median ratio of 9.0 and 100% positivity. ELISpot responses in patients were significantly (p < 0.001) reduced to ≤33% of the controls. After the second vaccination, female HSCT patients and female healthy controls showed significantly higher antibody responses than males (6.0 vs. 2.1 and 9.2 vs. 8.2, respectively; p < 0.05). Cellular immunity was diminished in patients irrespective of sex. In conclusion, especially male HSCT recipients showed impaired antibody responses after SARS-CoV-2 vaccination. Changing the vaccine schedule or composition could help increase vaccine responses. MDPI 2021-09-25 /pmc/articles/PMC8537291/ /pubmed/34696183 http://dx.doi.org/10.3390/vaccines9101075 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lindemann, Monika
Klisanin, Vesna
Thümmler, Laura
Fisenkci, Neslinur
Tsachakis-Mück, Nikolaos
Ditschkowski, Markus
Schwarzkopf, Sina
Klump, Hannes
Reinhardt, Hans Christian
Horn, Peter A.
Koldehoff, Michael
Humoral and Cellular Vaccination Responses against SARS-CoV-2 in Hematopoietic Stem Cell Transplant Recipients
title Humoral and Cellular Vaccination Responses against SARS-CoV-2 in Hematopoietic Stem Cell Transplant Recipients
title_full Humoral and Cellular Vaccination Responses against SARS-CoV-2 in Hematopoietic Stem Cell Transplant Recipients
title_fullStr Humoral and Cellular Vaccination Responses against SARS-CoV-2 in Hematopoietic Stem Cell Transplant Recipients
title_full_unstemmed Humoral and Cellular Vaccination Responses against SARS-CoV-2 in Hematopoietic Stem Cell Transplant Recipients
title_short Humoral and Cellular Vaccination Responses against SARS-CoV-2 in Hematopoietic Stem Cell Transplant Recipients
title_sort humoral and cellular vaccination responses against sars-cov-2 in hematopoietic stem cell transplant recipients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537291/
https://www.ncbi.nlm.nih.gov/pubmed/34696183
http://dx.doi.org/10.3390/vaccines9101075
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