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Predictors of Covid-19 Vaccination Response After In-Vivo T-Cell–Depleted Stem Cell Transplantation

Covid-19 vaccination is recommended in allogeneic transplant recipients, but many questions remain regarding its efficacy. Here we studied serologic responses in 145 patients who had undergone allogeneic transplantation using in vivo T-cell depletion. Median age was 57 (range 21-79) at transplantati...

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Autores principales: Chaekal, Ok-kyong, Gomez-Arteaga, Alexandra, Chen, Zhengming, Soave, Rosemary, Shore, Tsiporah, Mayer, Sebastian, Phillips, Adrienne, Hsu, Jing Mei, Drelick, Alexander, Kodiyanplakkal, Rosy Priya L., Plate, Markus, Satlin, Michael J., van Besien, Koen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213029/
https://www.ncbi.nlm.nih.gov/pubmed/35724850
http://dx.doi.org/10.1016/j.jtct.2022.06.012
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author Chaekal, Ok-kyong
Gomez-Arteaga, Alexandra
Chen, Zhengming
Soave, Rosemary
Shore, Tsiporah
Mayer, Sebastian
Phillips, Adrienne
Hsu, Jing Mei
Drelick, Alexander
Kodiyanplakkal, Rosy Priya L.
Plate, Markus
Satlin, Michael J.
van Besien, Koen
author_facet Chaekal, Ok-kyong
Gomez-Arteaga, Alexandra
Chen, Zhengming
Soave, Rosemary
Shore, Tsiporah
Mayer, Sebastian
Phillips, Adrienne
Hsu, Jing Mei
Drelick, Alexander
Kodiyanplakkal, Rosy Priya L.
Plate, Markus
Satlin, Michael J.
van Besien, Koen
author_sort Chaekal, Ok-kyong
collection PubMed
description Covid-19 vaccination is recommended in allogeneic transplant recipients, but many questions remain regarding its efficacy. Here we studied serologic responses in 145 patients who had undergone allogeneic transplantation using in vivo T-cell depletion. Median age was 57 (range 21-79) at transplantation and 61 (range 24-80) at vaccination. Sixty-nine percent were Caucasian. One third each received transplants from HLA-identical related (MRD), adult unrelated (MUD), or haploidentical-cord blood donors. Graft-versus-host disease (GVHD) prophylaxis involved in-vivo T-cell depletion using alemtuzumab for MRD or MUD transplants and anti-thymocyte globulin for haplo-cord transplants. Patients were vaccinated between January 2021 and January 2022, an average of 31 months (range 3-111 months) after transplantation. Sixty-one percent received the BNT162b2 (bioNtech/Pfizer) vaccine, 34% received mRNA-1273 (Moderna), and 5% received JNJ-78436735 (Johnson & Johnson). After the initial vaccinations (2 doses for BNT162b2 and mRNA-1273, 1 dose for JNJ-7843673), 124 of the 145 (85%) patients had a detectable SARS-CoV-2 spike protein (S) antibody, and 21 (15%) did not respond. Ninety-nine (68%) had high-level responses (≥100 binding antibody units [BAU]/mL)m and 25 (17%) had a low-level response (<100 BAU/mL). In multivariable analysis, lymphocyte count less than 1 × 10(9)/ mL, having chronic GVHD, and being vaccinated in the first year after transplantation emerged as independent predictors for poor response. Neither donor source nor prior exposure to rituximab was predictive of antibody response. SARS-CoV-2 vaccination induced generally high response rates in recipients of allogeneic transplants including recipients of umbilical cord blood transplants and after in-vivo T cell depletion. Responses are less robust in those vaccinated in the first year after transplantation, those with low lymphocyte counts, and those with chronic GVHD.
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spelling pubmed-92130292022-06-22 Predictors of Covid-19 Vaccination Response After In-Vivo T-Cell–Depleted Stem Cell Transplantation Chaekal, Ok-kyong Gomez-Arteaga, Alexandra Chen, Zhengming Soave, Rosemary Shore, Tsiporah Mayer, Sebastian Phillips, Adrienne Hsu, Jing Mei Drelick, Alexander Kodiyanplakkal, Rosy Priya L. Plate, Markus Satlin, Michael J. van Besien, Koen Transplant Cell Ther Full Length Article Covid-19 vaccination is recommended in allogeneic transplant recipients, but many questions remain regarding its efficacy. Here we studied serologic responses in 145 patients who had undergone allogeneic transplantation using in vivo T-cell depletion. Median age was 57 (range 21-79) at transplantation and 61 (range 24-80) at vaccination. Sixty-nine percent were Caucasian. One third each received transplants from HLA-identical related (MRD), adult unrelated (MUD), or haploidentical-cord blood donors. Graft-versus-host disease (GVHD) prophylaxis involved in-vivo T-cell depletion using alemtuzumab for MRD or MUD transplants and anti-thymocyte globulin for haplo-cord transplants. Patients were vaccinated between January 2021 and January 2022, an average of 31 months (range 3-111 months) after transplantation. Sixty-one percent received the BNT162b2 (bioNtech/Pfizer) vaccine, 34% received mRNA-1273 (Moderna), and 5% received JNJ-78436735 (Johnson & Johnson). After the initial vaccinations (2 doses for BNT162b2 and mRNA-1273, 1 dose for JNJ-7843673), 124 of the 145 (85%) patients had a detectable SARS-CoV-2 spike protein (S) antibody, and 21 (15%) did not respond. Ninety-nine (68%) had high-level responses (≥100 binding antibody units [BAU]/mL)m and 25 (17%) had a low-level response (<100 BAU/mL). In multivariable analysis, lymphocyte count less than 1 × 10(9)/ mL, having chronic GVHD, and being vaccinated in the first year after transplantation emerged as independent predictors for poor response. Neither donor source nor prior exposure to rituximab was predictive of antibody response. SARS-CoV-2 vaccination induced generally high response rates in recipients of allogeneic transplants including recipients of umbilical cord blood transplants and after in-vivo T cell depletion. Responses are less robust in those vaccinated in the first year after transplantation, those with low lymphocyte counts, and those with chronic GVHD. The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. 2022-09 2022-06-18 /pmc/articles/PMC9213029/ /pubmed/35724850 http://dx.doi.org/10.1016/j.jtct.2022.06.012 Text en © 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved. 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 Full Length Article
Chaekal, Ok-kyong
Gomez-Arteaga, Alexandra
Chen, Zhengming
Soave, Rosemary
Shore, Tsiporah
Mayer, Sebastian
Phillips, Adrienne
Hsu, Jing Mei
Drelick, Alexander
Kodiyanplakkal, Rosy Priya L.
Plate, Markus
Satlin, Michael J.
van Besien, Koen
Predictors of Covid-19 Vaccination Response After In-Vivo T-Cell–Depleted Stem Cell Transplantation
title Predictors of Covid-19 Vaccination Response After In-Vivo T-Cell–Depleted Stem Cell Transplantation
title_full Predictors of Covid-19 Vaccination Response After In-Vivo T-Cell–Depleted Stem Cell Transplantation
title_fullStr Predictors of Covid-19 Vaccination Response After In-Vivo T-Cell–Depleted Stem Cell Transplantation
title_full_unstemmed Predictors of Covid-19 Vaccination Response After In-Vivo T-Cell–Depleted Stem Cell Transplantation
title_short Predictors of Covid-19 Vaccination Response After In-Vivo T-Cell–Depleted Stem Cell Transplantation
title_sort predictors of covid-19 vaccination response after in-vivo t-cell–depleted stem cell transplantation
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213029/
https://www.ncbi.nlm.nih.gov/pubmed/35724850
http://dx.doi.org/10.1016/j.jtct.2022.06.012
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