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Thymectomy in Juvenile Myasthenia Gravis Is Safe Regarding Long Term Immunological Effects

Thymectomy is an established treatment in adult MG and also recommended for the treatment of post-pubertal onset juvenile MG. Whether the youngest children should be thymectomized is still debated. Signs of premature aging of the immune system have been shown in studies on early perioperative thymec...

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Autores principales: Popperud, Trine H., Gul, Kiran A., Brunborg, Cathrine, Olaussen, Richard W., Abrahamsen, Tore G., Osnes, Liv T., Kerty, Emila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947605/
https://www.ncbi.nlm.nih.gov/pubmed/33716918
http://dx.doi.org/10.3389/fneur.2021.596859
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author Popperud, Trine H.
Gul, Kiran A.
Brunborg, Cathrine
Olaussen, Richard W.
Abrahamsen, Tore G.
Osnes, Liv T.
Kerty, Emila
author_facet Popperud, Trine H.
Gul, Kiran A.
Brunborg, Cathrine
Olaussen, Richard W.
Abrahamsen, Tore G.
Osnes, Liv T.
Kerty, Emila
author_sort Popperud, Trine H.
collection PubMed
description Thymectomy is an established treatment in adult MG and also recommended for the treatment of post-pubertal onset juvenile MG. Whether the youngest children should be thymectomized is still debated. Signs of premature aging of the immune system have been shown in studies on early perioperative thymectomy in children with congenital heart defect. In this retrospective cohort study the objective was to investigate the long-term effects of treatment related thymectomy on T cell subsets and T cell receptor rearrangement excision circles (TRECs) in peripheral blood of juvenile myasthenia gravis (MG) patients, as well as clinical occurrence of autoimmune disorders, malignancies and infectious diseases. Forty-seven patients with onset of myasthenia gravis before the age of 19 years were included; 32 (68.1%) had been thymectomized and 15 (31.8%) had not. They were studied at varying times after thymectomy (7–26 years). We found a significant lower number of naïve helper T cells (CD4+CD45RA+) with an increased proportion of memory helper T cells (CD4+CD45RO+), and a significant lower number of naïve cytotoxic T cells (CD8+CD27+CD28+) in the thymectomized patients. In addition they showed a significant reduction in the number of TRECs and proportion of recent thymic emigrants (RTE) compared to non-thymectomized patients. In none of them an increased frequency of malignancies or infections was found. Our findings indicate a premature aging of the immune system after thymectomy in juvenile MG, but associated clinical consequences could not be verified.
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spelling pubmed-79476052021-03-12 Thymectomy in Juvenile Myasthenia Gravis Is Safe Regarding Long Term Immunological Effects Popperud, Trine H. Gul, Kiran A. Brunborg, Cathrine Olaussen, Richard W. Abrahamsen, Tore G. Osnes, Liv T. Kerty, Emila Front Neurol Neurology Thymectomy is an established treatment in adult MG and also recommended for the treatment of post-pubertal onset juvenile MG. Whether the youngest children should be thymectomized is still debated. Signs of premature aging of the immune system have been shown in studies on early perioperative thymectomy in children with congenital heart defect. In this retrospective cohort study the objective was to investigate the long-term effects of treatment related thymectomy on T cell subsets and T cell receptor rearrangement excision circles (TRECs) in peripheral blood of juvenile myasthenia gravis (MG) patients, as well as clinical occurrence of autoimmune disorders, malignancies and infectious diseases. Forty-seven patients with onset of myasthenia gravis before the age of 19 years were included; 32 (68.1%) had been thymectomized and 15 (31.8%) had not. They were studied at varying times after thymectomy (7–26 years). We found a significant lower number of naïve helper T cells (CD4+CD45RA+) with an increased proportion of memory helper T cells (CD4+CD45RO+), and a significant lower number of naïve cytotoxic T cells (CD8+CD27+CD28+) in the thymectomized patients. In addition they showed a significant reduction in the number of TRECs and proportion of recent thymic emigrants (RTE) compared to non-thymectomized patients. In none of them an increased frequency of malignancies or infections was found. Our findings indicate a premature aging of the immune system after thymectomy in juvenile MG, but associated clinical consequences could not be verified. Frontiers Media S.A. 2021-02-25 /pmc/articles/PMC7947605/ /pubmed/33716918 http://dx.doi.org/10.3389/fneur.2021.596859 Text en Copyright © 2021 Popperud, Gul, Brunborg, Olaussen, Abrahamsen, Osnes and Kerty. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Popperud, Trine H.
Gul, Kiran A.
Brunborg, Cathrine
Olaussen, Richard W.
Abrahamsen, Tore G.
Osnes, Liv T.
Kerty, Emila
Thymectomy in Juvenile Myasthenia Gravis Is Safe Regarding Long Term Immunological Effects
title Thymectomy in Juvenile Myasthenia Gravis Is Safe Regarding Long Term Immunological Effects
title_full Thymectomy in Juvenile Myasthenia Gravis Is Safe Regarding Long Term Immunological Effects
title_fullStr Thymectomy in Juvenile Myasthenia Gravis Is Safe Regarding Long Term Immunological Effects
title_full_unstemmed Thymectomy in Juvenile Myasthenia Gravis Is Safe Regarding Long Term Immunological Effects
title_short Thymectomy in Juvenile Myasthenia Gravis Is Safe Regarding Long Term Immunological Effects
title_sort thymectomy in juvenile myasthenia gravis is safe regarding long term immunological effects
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947605/
https://www.ncbi.nlm.nih.gov/pubmed/33716918
http://dx.doi.org/10.3389/fneur.2021.596859
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