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SARS-CoV-2 Vaccine-Induced Immune Responses Among Hematopoietic Stem Cell Transplant Recipients

BACKGROUND: Although severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination reduces the risk and severity of coronavirus disease 2019 (COVID-19), several variables may impact the humoral response among patients undergoing hematopoietic stem cell transplantation (HSCT). METHODS: A r...

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Autores principales: Kokogho, Afoke, Crowell, Trevor A, Aleissa, Muneerah, Lupan, Ana-Mihaela, Davey, Sonya, Park Chang, Jun Bai, Baden, Lindsey R, Walsh, Stephen R, Sherman, Amy C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372870/
https://www.ncbi.nlm.nih.gov/pubmed/37520415
http://dx.doi.org/10.1093/ofid/ofad349
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author Kokogho, Afoke
Crowell, Trevor A
Aleissa, Muneerah
Lupan, Ana-Mihaela
Davey, Sonya
Park Chang, Jun Bai
Baden, Lindsey R
Walsh, Stephen R
Sherman, Amy C
author_facet Kokogho, Afoke
Crowell, Trevor A
Aleissa, Muneerah
Lupan, Ana-Mihaela
Davey, Sonya
Park Chang, Jun Bai
Baden, Lindsey R
Walsh, Stephen R
Sherman, Amy C
author_sort Kokogho, Afoke
collection PubMed
description BACKGROUND: Although severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination reduces the risk and severity of coronavirus disease 2019 (COVID-19), several variables may impact the humoral response among patients undergoing hematopoietic stem cell transplantation (HSCT). METHODS: A retrospective chart review was conducted among SARS-CoV-2-vaccinated HSCT recipients between 2020 and 2022 at a single center in Boston, Massachusetts. Patients age ≥18 years who received doses of Pfizer, Moderna, or J&J vaccines were included. Anti-spike (S) immunoglobulin G (IgG) titer levels were measured using the Roche assay. Responders (≥0.8 U/mL) and nonresponders (<0.8 U/mL) were categorized and analyzed. Multivariable linear and logistic regression were used to estimate the correlation coefficient and odds ratio of response magnitude and status. RESULTS: Of 152 HSCT recipients, 141 (92.8%) were responders, with a median (interquartile range [IQR]) anti-S IgG titer of 2500 (107.9–2500) U/mL at a median (IQR) of 80.5 (36–153.5) days from last dose, regardless of the number of doses received. Higher quantitative titers were associated with receipt of more vaccine doses (coeff, 205.79; 95% CI, 30.10 to 381.47; P = .022), being female (coeff, 343.5; 95% CI, −682.6 to −4.4; P = .047), being younger (<65 years; coeff, 365.2; 95% CI, −711.3 to 19.1; P = .039), and not being on anti-CD20 therapy (coeff, −1163.7; 95% CI, −1717.7 to −609.7; P = .001). Being male (odds ratio [OR], 0.11; 95% CI, 0.01 to 0.93; P = .04) and being on anti-CD20 therapy (OR, 0.16; 95% CI, 0.03 to 0.70; P = .016) were associated with nonresponse. CONCLUSIONS: Overall, most HSCT recipients had high SARS-CoV-2 antibody responses. More vaccine doses improved the magnitude of immune responses. Anti-S IgG monitoring may be useful for identifying attenuated vaccine-induced responses.
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spelling pubmed-103728702023-07-28 SARS-CoV-2 Vaccine-Induced Immune Responses Among Hematopoietic Stem Cell Transplant Recipients Kokogho, Afoke Crowell, Trevor A Aleissa, Muneerah Lupan, Ana-Mihaela Davey, Sonya Park Chang, Jun Bai Baden, Lindsey R Walsh, Stephen R Sherman, Amy C Open Forum Infect Dis Major Article BACKGROUND: Although severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination reduces the risk and severity of coronavirus disease 2019 (COVID-19), several variables may impact the humoral response among patients undergoing hematopoietic stem cell transplantation (HSCT). METHODS: A retrospective chart review was conducted among SARS-CoV-2-vaccinated HSCT recipients between 2020 and 2022 at a single center in Boston, Massachusetts. Patients age ≥18 years who received doses of Pfizer, Moderna, or J&J vaccines were included. Anti-spike (S) immunoglobulin G (IgG) titer levels were measured using the Roche assay. Responders (≥0.8 U/mL) and nonresponders (<0.8 U/mL) were categorized and analyzed. Multivariable linear and logistic regression were used to estimate the correlation coefficient and odds ratio of response magnitude and status. RESULTS: Of 152 HSCT recipients, 141 (92.8%) were responders, with a median (interquartile range [IQR]) anti-S IgG titer of 2500 (107.9–2500) U/mL at a median (IQR) of 80.5 (36–153.5) days from last dose, regardless of the number of doses received. Higher quantitative titers were associated with receipt of more vaccine doses (coeff, 205.79; 95% CI, 30.10 to 381.47; P = .022), being female (coeff, 343.5; 95% CI, −682.6 to −4.4; P = .047), being younger (<65 years; coeff, 365.2; 95% CI, −711.3 to 19.1; P = .039), and not being on anti-CD20 therapy (coeff, −1163.7; 95% CI, −1717.7 to −609.7; P = .001). Being male (odds ratio [OR], 0.11; 95% CI, 0.01 to 0.93; P = .04) and being on anti-CD20 therapy (OR, 0.16; 95% CI, 0.03 to 0.70; P = .016) were associated with nonresponse. CONCLUSIONS: Overall, most HSCT recipients had high SARS-CoV-2 antibody responses. More vaccine doses improved the magnitude of immune responses. Anti-S IgG monitoring may be useful for identifying attenuated vaccine-induced responses. Oxford University Press 2023-07-10 /pmc/articles/PMC10372870/ /pubmed/37520415 http://dx.doi.org/10.1093/ofid/ofad349 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Kokogho, Afoke
Crowell, Trevor A
Aleissa, Muneerah
Lupan, Ana-Mihaela
Davey, Sonya
Park Chang, Jun Bai
Baden, Lindsey R
Walsh, Stephen R
Sherman, Amy C
SARS-CoV-2 Vaccine-Induced Immune Responses Among Hematopoietic Stem Cell Transplant Recipients
title SARS-CoV-2 Vaccine-Induced Immune Responses Among Hematopoietic Stem Cell Transplant Recipients
title_full SARS-CoV-2 Vaccine-Induced Immune Responses Among Hematopoietic Stem Cell Transplant Recipients
title_fullStr SARS-CoV-2 Vaccine-Induced Immune Responses Among Hematopoietic Stem Cell Transplant Recipients
title_full_unstemmed SARS-CoV-2 Vaccine-Induced Immune Responses Among Hematopoietic Stem Cell Transplant Recipients
title_short SARS-CoV-2 Vaccine-Induced Immune Responses Among Hematopoietic Stem Cell Transplant Recipients
title_sort sars-cov-2 vaccine-induced immune responses among hematopoietic stem cell transplant recipients
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372870/
https://www.ncbi.nlm.nih.gov/pubmed/37520415
http://dx.doi.org/10.1093/ofid/ofad349
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