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Post-transplant absolute lymphocyte count predicts early cytomegalovirus infection after heart transplantation

Immunosuppressive therapy can decrease rejection episodes and increase the risk of severe and fatal infections in heart transplantation (HT) recipients. Immunosuppressive therapy can also decrease the absolute lymphocyte count (ALC), but the relationship between early post-transplant ALC and early c...

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Autores principales: Yoon, Minjae, Oh, Jaewon, Chun, Kyeong-Hyeon, Lee, Chan Joo, Kang, Seok-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809401/
https://www.ncbi.nlm.nih.gov/pubmed/33446808
http://dx.doi.org/10.1038/s41598-020-80790-4
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author Yoon, Minjae
Oh, Jaewon
Chun, Kyeong-Hyeon
Lee, Chan Joo
Kang, Seok-Min
author_facet Yoon, Minjae
Oh, Jaewon
Chun, Kyeong-Hyeon
Lee, Chan Joo
Kang, Seok-Min
author_sort Yoon, Minjae
collection PubMed
description Immunosuppressive therapy can decrease rejection episodes and increase the risk of severe and fatal infections in heart transplantation (HT) recipients. Immunosuppressive therapy can also decrease the absolute lymphocyte count (ALC), but the relationship between early post-transplant ALC and early cytomegalovirus (CMV) infection is largely unknown, especially in HT. We retrospectively analyzed 58 HT recipients who tested positive for CMV IgG antibody and received basiliximab induction therapy. We collected preoperative and 2-month postoperative data on ALC and CMV load. The CMV load > 1200 IU/mL was used as the cutoff value to define early CMV infection. Post-transplant lymphopenia was defined as an ALC of < 500 cells/μL at postoperative day (POD) #7. On POD #7, 29 (50.0%) patients had post-transplant lymphopenia and 29 (50.0%) patients did not. The incidence of CMV infection within 1 or 2 months of HT was higher in the post-transplant lymphopenia group than in the non-lymphopenia group (82.8% vs. 48.3%, P = 0.013; 89.7% vs. 65.5%, P = 0.028, respectively). ALC < 500 cells/μL on POD #7 was an independent risk factor for early CMV infection within 1 month of HT (odds ratio, 4.14; 95% confidence interval, 1.16–14.77; P = 0.029). A low ALC after HT was associated with a high risk of early CMV infection. Post-transplant ALC monitoring is simple and inexpensive and can help identify patients at high risk of early CMV infection.
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spelling pubmed-78094012021-01-15 Post-transplant absolute lymphocyte count predicts early cytomegalovirus infection after heart transplantation Yoon, Minjae Oh, Jaewon Chun, Kyeong-Hyeon Lee, Chan Joo Kang, Seok-Min Sci Rep Article Immunosuppressive therapy can decrease rejection episodes and increase the risk of severe and fatal infections in heart transplantation (HT) recipients. Immunosuppressive therapy can also decrease the absolute lymphocyte count (ALC), but the relationship between early post-transplant ALC and early cytomegalovirus (CMV) infection is largely unknown, especially in HT. We retrospectively analyzed 58 HT recipients who tested positive for CMV IgG antibody and received basiliximab induction therapy. We collected preoperative and 2-month postoperative data on ALC and CMV load. The CMV load > 1200 IU/mL was used as the cutoff value to define early CMV infection. Post-transplant lymphopenia was defined as an ALC of < 500 cells/μL at postoperative day (POD) #7. On POD #7, 29 (50.0%) patients had post-transplant lymphopenia and 29 (50.0%) patients did not. The incidence of CMV infection within 1 or 2 months of HT was higher in the post-transplant lymphopenia group than in the non-lymphopenia group (82.8% vs. 48.3%, P = 0.013; 89.7% vs. 65.5%, P = 0.028, respectively). ALC < 500 cells/μL on POD #7 was an independent risk factor for early CMV infection within 1 month of HT (odds ratio, 4.14; 95% confidence interval, 1.16–14.77; P = 0.029). A low ALC after HT was associated with a high risk of early CMV infection. Post-transplant ALC monitoring is simple and inexpensive and can help identify patients at high risk of early CMV infection. Nature Publishing Group UK 2021-01-14 /pmc/articles/PMC7809401/ /pubmed/33446808 http://dx.doi.org/10.1038/s41598-020-80790-4 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yoon, Minjae
Oh, Jaewon
Chun, Kyeong-Hyeon
Lee, Chan Joo
Kang, Seok-Min
Post-transplant absolute lymphocyte count predicts early cytomegalovirus infection after heart transplantation
title Post-transplant absolute lymphocyte count predicts early cytomegalovirus infection after heart transplantation
title_full Post-transplant absolute lymphocyte count predicts early cytomegalovirus infection after heart transplantation
title_fullStr Post-transplant absolute lymphocyte count predicts early cytomegalovirus infection after heart transplantation
title_full_unstemmed Post-transplant absolute lymphocyte count predicts early cytomegalovirus infection after heart transplantation
title_short Post-transplant absolute lymphocyte count predicts early cytomegalovirus infection after heart transplantation
title_sort post-transplant absolute lymphocyte count predicts early cytomegalovirus infection after heart transplantation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809401/
https://www.ncbi.nlm.nih.gov/pubmed/33446808
http://dx.doi.org/10.1038/s41598-020-80790-4
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