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Antibody response to COVID-19 vaccine in 130 recipients of hematopoietic stem cell transplantation

We evaluated anti-spike protein antibody (anti-S) production in 130 hematopoietic stem cell transplant (HSCT) recipients who received the coronavirus disease-2019 vaccine. Sixty-five received allo-HSCT and 65 received auto-HSCT. Disease-specific treatments were being administered to 43.1% of allo-HS...

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Autores principales: Tsushima, Takafumi, Terao, Toshiki, Narita, Kentaro, Fukumoto, Ami, Ikeda, Daisuke, Kamura, Yuya, Kuzume, Ayumi, Tabata, Rikako, Miura, Daisuke, Takeuchi, Masami, Matsue, Kosei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011370/
https://www.ncbi.nlm.nih.gov/pubmed/35426579
http://dx.doi.org/10.1007/s12185-022-03325-9
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author Tsushima, Takafumi
Terao, Toshiki
Narita, Kentaro
Fukumoto, Ami
Ikeda, Daisuke
Kamura, Yuya
Kuzume, Ayumi
Tabata, Rikako
Miura, Daisuke
Takeuchi, Masami
Matsue, Kosei
author_facet Tsushima, Takafumi
Terao, Toshiki
Narita, Kentaro
Fukumoto, Ami
Ikeda, Daisuke
Kamura, Yuya
Kuzume, Ayumi
Tabata, Rikako
Miura, Daisuke
Takeuchi, Masami
Matsue, Kosei
author_sort Tsushima, Takafumi
collection PubMed
description We evaluated anti-spike protein antibody (anti-S) production in 130 hematopoietic stem cell transplant (HSCT) recipients who received the coronavirus disease-2019 vaccine. Sixty-five received allo-HSCT and 65 received auto-HSCT. Disease-specific treatments were being administered to 43.1% of allo-HSCT and 69.2% of auto-HSCT patients. Seropositivity was observed in 87.7% of allo-HSCT and 89.2% in auto-HSCT patients. Anti-S antibody production was significantly impaired in auto-HSCT patients compared with controls (178U/mL [0.4–4990.0] vs. 669 U/mL [40.3–4377.0], p < 0.001), but not in allo-HSCT patients (900 U/mL [0.4–12,893.0] vs. 860 U/mL [40.3–8988.0], P = 0.659). Clinically relevant anti-S antibody levels (> 264 U/mL) were achieved in 59.2% of patients (76.9% in allo-HSCT and 41.5% in auto-HSCT). The main factors influencing the protective level of the antibody response were the CD19 + cell count and serum immunoglobulin G levels, and these were significant in both allo-HSCT and auto-HSCT patients. Other factors included time since HSCT, complete remission status, use of immunosuppressive drugs, and levels of lymphocyte subsets including CD4, CD8 and CD56 positive cells, but these were only significant in allo-HSCT patients. Allo-HSCT patients had a relatively favorable antibody response, while auto-HSCT patients had poorer results. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12185-022-03325-9.
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spelling pubmed-90113702022-04-15 Antibody response to COVID-19 vaccine in 130 recipients of hematopoietic stem cell transplantation Tsushima, Takafumi Terao, Toshiki Narita, Kentaro Fukumoto, Ami Ikeda, Daisuke Kamura, Yuya Kuzume, Ayumi Tabata, Rikako Miura, Daisuke Takeuchi, Masami Matsue, Kosei Int J Hematol Rapid Communication We evaluated anti-spike protein antibody (anti-S) production in 130 hematopoietic stem cell transplant (HSCT) recipients who received the coronavirus disease-2019 vaccine. Sixty-five received allo-HSCT and 65 received auto-HSCT. Disease-specific treatments were being administered to 43.1% of allo-HSCT and 69.2% of auto-HSCT patients. Seropositivity was observed in 87.7% of allo-HSCT and 89.2% in auto-HSCT patients. Anti-S antibody production was significantly impaired in auto-HSCT patients compared with controls (178U/mL [0.4–4990.0] vs. 669 U/mL [40.3–4377.0], p < 0.001), but not in allo-HSCT patients (900 U/mL [0.4–12,893.0] vs. 860 U/mL [40.3–8988.0], P = 0.659). Clinically relevant anti-S antibody levels (> 264 U/mL) were achieved in 59.2% of patients (76.9% in allo-HSCT and 41.5% in auto-HSCT). The main factors influencing the protective level of the antibody response were the CD19 + cell count and serum immunoglobulin G levels, and these were significant in both allo-HSCT and auto-HSCT patients. Other factors included time since HSCT, complete remission status, use of immunosuppressive drugs, and levels of lymphocyte subsets including CD4, CD8 and CD56 positive cells, but these were only significant in allo-HSCT patients. Allo-HSCT patients had a relatively favorable antibody response, while auto-HSCT patients had poorer results. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12185-022-03325-9. Springer Nature Singapore 2022-04-15 2022 /pmc/articles/PMC9011370/ /pubmed/35426579 http://dx.doi.org/10.1007/s12185-022-03325-9 Text en © Japanese Society of Hematology 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Rapid Communication
Tsushima, Takafumi
Terao, Toshiki
Narita, Kentaro
Fukumoto, Ami
Ikeda, Daisuke
Kamura, Yuya
Kuzume, Ayumi
Tabata, Rikako
Miura, Daisuke
Takeuchi, Masami
Matsue, Kosei
Antibody response to COVID-19 vaccine in 130 recipients of hematopoietic stem cell transplantation
title Antibody response to COVID-19 vaccine in 130 recipients of hematopoietic stem cell transplantation
title_full Antibody response to COVID-19 vaccine in 130 recipients of hematopoietic stem cell transplantation
title_fullStr Antibody response to COVID-19 vaccine in 130 recipients of hematopoietic stem cell transplantation
title_full_unstemmed Antibody response to COVID-19 vaccine in 130 recipients of hematopoietic stem cell transplantation
title_short Antibody response to COVID-19 vaccine in 130 recipients of hematopoietic stem cell transplantation
title_sort antibody response to covid-19 vaccine in 130 recipients of hematopoietic stem cell transplantation
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011370/
https://www.ncbi.nlm.nih.gov/pubmed/35426579
http://dx.doi.org/10.1007/s12185-022-03325-9
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