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Factors associated with cytomegalovirus infection in children undergoing allogeneic hematopoietic stem-cell transplantation

While preemptive therapy with ganciclovir (GCV) for cytomegalovirus (CMV) infection is used following allogeneic hematopoietic stem-cell transplantation (HSCT), risk factors for CMV infection in children undergoing HSCT are poorly understood. We studied CMV reactivation following allogeneic HSCT by...

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Autores principales: Jaing, Tang-Her, Chang, Tsung-Yen, Chen, Shih-Hsiang, Wen, Yu-Chuan, Yu, Ting-Jiuan, Lee, Ching-Fen, Yang, Chao-Ping, Tsay, Pei-Kwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358375/
https://www.ncbi.nlm.nih.gov/pubmed/30681583
http://dx.doi.org/10.1097/MD.0000000000014172
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author Jaing, Tang-Her
Chang, Tsung-Yen
Chen, Shih-Hsiang
Wen, Yu-Chuan
Yu, Ting-Jiuan
Lee, Ching-Fen
Yang, Chao-Ping
Tsay, Pei-Kwei
author_facet Jaing, Tang-Her
Chang, Tsung-Yen
Chen, Shih-Hsiang
Wen, Yu-Chuan
Yu, Ting-Jiuan
Lee, Ching-Fen
Yang, Chao-Ping
Tsay, Pei-Kwei
author_sort Jaing, Tang-Her
collection PubMed
description While preemptive therapy with ganciclovir (GCV) for cytomegalovirus (CMV) infection is used following allogeneic hematopoietic stem-cell transplantation (HSCT), risk factors for CMV infection in children undergoing HSCT are poorly understood. We studied CMV reactivation following allogeneic HSCT by retrospectively analyzing pediatric patients who received allogeneic HSCT and preemptive GCV therapy between 1998 and 2016. The level of viremia requiring preemptive GCV therapy was >1 CMV antigen-positive cells per 5 × 10(5) leukocytes during the antigenemia assay era and >1000 copies/mL in the polymerase chain reaction era. Among 290 at-risk patients, 54 (18.6%) patients had primary CMV infection or CMV reactivation occurring at a median of 76 days (range, 7–234) following HSCT. CMV reactivation occurred in 28.2% (44/156) of CMV-seropositive transplant recipients at a median of 26 days posttransplant. Univariate and multivariate analyses revealed statistically significant relationships between CMV infection and grade III–IV acute graft-vs-host disease, seronegative donor/seropositive recipient combination, and unrelated/mismatched donors. The remaining demographic factors were not predictive of CMV infection. The seronegative donor/seropositive recipient combination for HSCT was associated with an incomplete response to antiviral therapy. Human leukocyte antigen identical donors were the best choice for patients undergoing allogeneic HSCT to reduce the incidence of CMV disease and mortality.
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spelling pubmed-63583752019-02-15 Factors associated with cytomegalovirus infection in children undergoing allogeneic hematopoietic stem-cell transplantation Jaing, Tang-Her Chang, Tsung-Yen Chen, Shih-Hsiang Wen, Yu-Chuan Yu, Ting-Jiuan Lee, Ching-Fen Yang, Chao-Ping Tsay, Pei-Kwei Medicine (Baltimore) Research Article While preemptive therapy with ganciclovir (GCV) for cytomegalovirus (CMV) infection is used following allogeneic hematopoietic stem-cell transplantation (HSCT), risk factors for CMV infection in children undergoing HSCT are poorly understood. We studied CMV reactivation following allogeneic HSCT by retrospectively analyzing pediatric patients who received allogeneic HSCT and preemptive GCV therapy between 1998 and 2016. The level of viremia requiring preemptive GCV therapy was >1 CMV antigen-positive cells per 5 × 10(5) leukocytes during the antigenemia assay era and >1000 copies/mL in the polymerase chain reaction era. Among 290 at-risk patients, 54 (18.6%) patients had primary CMV infection or CMV reactivation occurring at a median of 76 days (range, 7–234) following HSCT. CMV reactivation occurred in 28.2% (44/156) of CMV-seropositive transplant recipients at a median of 26 days posttransplant. Univariate and multivariate analyses revealed statistically significant relationships between CMV infection and grade III–IV acute graft-vs-host disease, seronegative donor/seropositive recipient combination, and unrelated/mismatched donors. The remaining demographic factors were not predictive of CMV infection. The seronegative donor/seropositive recipient combination for HSCT was associated with an incomplete response to antiviral therapy. Human leukocyte antigen identical donors were the best choice for patients undergoing allogeneic HSCT to reduce the incidence of CMV disease and mortality. Wolters Kluwer Health 2019-01-25 /pmc/articles/PMC6358375/ /pubmed/30681583 http://dx.doi.org/10.1097/MD.0000000000014172 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle Research Article
Jaing, Tang-Her
Chang, Tsung-Yen
Chen, Shih-Hsiang
Wen, Yu-Chuan
Yu, Ting-Jiuan
Lee, Ching-Fen
Yang, Chao-Ping
Tsay, Pei-Kwei
Factors associated with cytomegalovirus infection in children undergoing allogeneic hematopoietic stem-cell transplantation
title Factors associated with cytomegalovirus infection in children undergoing allogeneic hematopoietic stem-cell transplantation
title_full Factors associated with cytomegalovirus infection in children undergoing allogeneic hematopoietic stem-cell transplantation
title_fullStr Factors associated with cytomegalovirus infection in children undergoing allogeneic hematopoietic stem-cell transplantation
title_full_unstemmed Factors associated with cytomegalovirus infection in children undergoing allogeneic hematopoietic stem-cell transplantation
title_short Factors associated with cytomegalovirus infection in children undergoing allogeneic hematopoietic stem-cell transplantation
title_sort factors associated with cytomegalovirus infection in children undergoing allogeneic hematopoietic stem-cell transplantation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358375/
https://www.ncbi.nlm.nih.gov/pubmed/30681583
http://dx.doi.org/10.1097/MD.0000000000014172
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