TY - JOUR
T1 - Efficacy and safety of mRNA1273 SARS-CoV-2 vaccination in hematopoietic stem cell transplant recipients
T2 - Single center experience
AU - Huguet, Maria
AU - Boigues, Marc
AU - Sorigué, Marc
AU - Blanco, Julià
AU - Quirant, Bibiana
AU - Ferrà, Christelle
AU - Morgades, Mireia
AU - Torrent, Anna
AU - Abril, Laura
AU - Sancho, Juan Manuel
AU - Pradenas, Edwards
AU - Marfil, Silvia
AU - Trinité, Benjamin
AU - Ferrà, Christelle
AU - Felip, Eudald
AU - Morán, Teresa
N1 - Copyright © 2023 Elsevier España, S.L.U. All rights reserved.
PY - 2024/4/12
Y1 - 2024/4/12
N2 - Background: COVID-19 represents a worldwide pandemic and vaccination remains the most effective preventive strategy. Among hematological patients, COVID-19 has been associated with a high mortality rate. Vaccination against SARS-CoV-2 has shown high efficacy in reducing community transmission, hospitalization and deaths related to severe COVID-19 disease. However, patients with impaired immunity may have lower sero-responsiveness to vaccination. Methods: This study focuses on hematopoietic stem cell transplantation (HSCT) recipients. We performed a unicenter, prospective, observational study of a cohort of 31 allogeneic and 56 autologous-HSCT recipients monitored between March 2021 and May 2021 for serological response after COVID-19 vaccination with two doses of mRNA1273 vaccine (Moderna). In order to determine seroconversion, serological status before vaccination was studied. Results: At a median range of 75 days after the second vaccine dose, seroconversion rates were 84% and 85% for the autologous and allogeneic-HSCT groups, respectively. We confirmed some potential risk factors for a negative serological response, such as receiving anti-CD20 therapy in the previous year before vaccination, a low B-lymphocyte count and hypogammaglobulinemia. Neutralizing antibodies were quantified in 44 patients, with a good correlation with serological tests. Adverse events were minimal. Conclusion: mRNA1273 vaccination is safe and effective in HSCT recipients, especially in those presenting recovered immunity.
AB - Background: COVID-19 represents a worldwide pandemic and vaccination remains the most effective preventive strategy. Among hematological patients, COVID-19 has been associated with a high mortality rate. Vaccination against SARS-CoV-2 has shown high efficacy in reducing community transmission, hospitalization and deaths related to severe COVID-19 disease. However, patients with impaired immunity may have lower sero-responsiveness to vaccination. Methods: This study focuses on hematopoietic stem cell transplantation (HSCT) recipients. We performed a unicenter, prospective, observational study of a cohort of 31 allogeneic and 56 autologous-HSCT recipients monitored between March 2021 and May 2021 for serological response after COVID-19 vaccination with two doses of mRNA1273 vaccine (Moderna). In order to determine seroconversion, serological status before vaccination was studied. Results: At a median range of 75 days after the second vaccine dose, seroconversion rates were 84% and 85% for the autologous and allogeneic-HSCT groups, respectively. We confirmed some potential risk factors for a negative serological response, such as receiving anti-CD20 therapy in the previous year before vaccination, a low B-lymphocyte count and hypogammaglobulinemia. Neutralizing antibodies were quantified in 44 patients, with a good correlation with serological tests. Adverse events were minimal. Conclusion: mRNA1273 vaccination is safe and effective in HSCT recipients, especially in those presenting recovered immunity.
KW - COVID-19
KW - HSCT recipients
KW - Vaccination
UR - http://www.scopus.com/inward/record.url?scp=85183687533&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/42ac88f5-8726-3398-90b8-6dc79bcecba9/
UR - https://portalrecerca.uab.cat/en/publications/cd596f20-8c93-4b36-ac3f-5a16ba8b5e7d
U2 - 10.1016/j.medcli.2023.10.016
DO - 10.1016/j.medcli.2023.10.016
M3 - Article
C2 - 38000941
AN - SCOPUS:85183687533
SN - 0025-7753
VL - 162
SP - 313
EP - 320
JO - Medicina clinica
JF - Medicina clinica
IS - 7
ER -