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The association of conditioning regimen with cytomegalovirus reactivation after allogeneic hematopoietic stem cell transplantation

BACKGROUND AND OBJECTIVES: Infections is yet one of the life-threatening complications of the hematopoietic stem cell transplantation (HSCT). The myeloablative and immunosuppressive conditioning regimens, which are administered before HSCT, dampen the defense capacity of the recipients’ immune syste...

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Autores principales: Mardani, Masoud, Abolghasemi, Sara, Shabani, Shiva, Tavakoli, Farzaneh, Saeedi, Anahita, Parkhideh, Sayeh, Hajifathali, Abbas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884275/
https://www.ncbi.nlm.nih.gov/pubmed/33613920
http://dx.doi.org/10.18502/ijm.v12i6.5040
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author Mardani, Masoud
Abolghasemi, Sara
Shabani, Shiva
Tavakoli, Farzaneh
Saeedi, Anahita
Parkhideh, Sayeh
Hajifathali, Abbas
author_facet Mardani, Masoud
Abolghasemi, Sara
Shabani, Shiva
Tavakoli, Farzaneh
Saeedi, Anahita
Parkhideh, Sayeh
Hajifathali, Abbas
author_sort Mardani, Masoud
collection PubMed
description BACKGROUND AND OBJECTIVES: Infections is yet one of the life-threatening complications of the hematopoietic stem cell transplantation (HSCT). The myeloablative and immunosuppressive conditioning regimens, which are administered before HSCT, dampen the defense capacity of the recipients’ immune systems. In this condition, opportunistic infections, especially viral infections such as cytomegalovirus (CMV) can be reactivated and cause morbidity and mortality in HSCT patients. Here, we aimed to find out any possible relationship between types of conditioning regimen and CMV reactivation in allogeneic HSCT patients. MATERIALS AND METHODS: We retrospectively analyzed the data of 145 CMV-seropositive cases out of total 201 allo-HSCT patients, including age, gender, underlying disease, conditioning regimen, prophylaxis regimen and occurrence of acute graft-versus-host disease (aGVHD) to evaluate their roles in CMV reactivation. RESULTS: Our result showed that conditioning regimen containing Busulfan and Fludarabine (P=0.003) or Cyclophospha-mide (P=0.02) significantly decrease the early CMV reactivation. Patients who developed aGVHD (P=0.003) and those who received anti-thymocyte globulin (ATG) as prophylaxis regimen (P=0.002), had 1.84 and 2.63 times higher risks of CMV reactivation, respectively. CONCLUSION: Our findings suggest the conditioning regimen, aGVHD and ATG as influencing factors for early CMV reactivation post-HSCT which should be considered in the future studies.
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spelling pubmed-78842752021-02-19 The association of conditioning regimen with cytomegalovirus reactivation after allogeneic hematopoietic stem cell transplantation Mardani, Masoud Abolghasemi, Sara Shabani, Shiva Tavakoli, Farzaneh Saeedi, Anahita Parkhideh, Sayeh Hajifathali, Abbas Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: Infections is yet one of the life-threatening complications of the hematopoietic stem cell transplantation (HSCT). The myeloablative and immunosuppressive conditioning regimens, which are administered before HSCT, dampen the defense capacity of the recipients’ immune systems. In this condition, opportunistic infections, especially viral infections such as cytomegalovirus (CMV) can be reactivated and cause morbidity and mortality in HSCT patients. Here, we aimed to find out any possible relationship between types of conditioning regimen and CMV reactivation in allogeneic HSCT patients. MATERIALS AND METHODS: We retrospectively analyzed the data of 145 CMV-seropositive cases out of total 201 allo-HSCT patients, including age, gender, underlying disease, conditioning regimen, prophylaxis regimen and occurrence of acute graft-versus-host disease (aGVHD) to evaluate their roles in CMV reactivation. RESULTS: Our result showed that conditioning regimen containing Busulfan and Fludarabine (P=0.003) or Cyclophospha-mide (P=0.02) significantly decrease the early CMV reactivation. Patients who developed aGVHD (P=0.003) and those who received anti-thymocyte globulin (ATG) as prophylaxis regimen (P=0.002), had 1.84 and 2.63 times higher risks of CMV reactivation, respectively. CONCLUSION: Our findings suggest the conditioning regimen, aGVHD and ATG as influencing factors for early CMV reactivation post-HSCT which should be considered in the future studies. Tehran University of Medical Sciences 2020-12 /pmc/articles/PMC7884275/ /pubmed/33613920 http://dx.doi.org/10.18502/ijm.v12i6.5040 Text en Copyright© 2020 The Authors. This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license, (https://creativecommons.org/licenses/by-nc/4.0/) Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Article
Mardani, Masoud
Abolghasemi, Sara
Shabani, Shiva
Tavakoli, Farzaneh
Saeedi, Anahita
Parkhideh, Sayeh
Hajifathali, Abbas
The association of conditioning regimen with cytomegalovirus reactivation after allogeneic hematopoietic stem cell transplantation
title The association of conditioning regimen with cytomegalovirus reactivation after allogeneic hematopoietic stem cell transplantation
title_full The association of conditioning regimen with cytomegalovirus reactivation after allogeneic hematopoietic stem cell transplantation
title_fullStr The association of conditioning regimen with cytomegalovirus reactivation after allogeneic hematopoietic stem cell transplantation
title_full_unstemmed The association of conditioning regimen with cytomegalovirus reactivation after allogeneic hematopoietic stem cell transplantation
title_short The association of conditioning regimen with cytomegalovirus reactivation after allogeneic hematopoietic stem cell transplantation
title_sort association of conditioning regimen with cytomegalovirus reactivation after allogeneic hematopoietic stem cell transplantation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884275/
https://www.ncbi.nlm.nih.gov/pubmed/33613920
http://dx.doi.org/10.18502/ijm.v12i6.5040
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