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Updated: Nov 13, 2025

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Published on: May 13, 2015
Thymectomy in Juvenile Myasthenia Gravis Is Safe Regarding Long Term Immunological Effects
Trine H Popperud1,2, Kiran A Gul2,3, Cathrine Brunborg4
1Department of Neurology, Oslo University Hospital, Oslo, Norway.
Insights
Thymectomy in juvenile myasthenia gravis patients may lead to premature immune system aging, indicated by altered T cell subsets and reduced thymic output. However, no increased clinical risks of infections or malignancies were observed long-term.
Area of Science:
- Immunology
- Pediatric Neurology
- Surgical Research
Background:
- Thymectomy is standard for adult myasthenia gravis (MG) and post-pubertal juvenile MG.
- Its use in younger children remains debated.
- Early thymectomy in other conditions suggests potential immune system aging.
Purpose of the Study:
- To investigate long-term effects of thymectomy on T cell subsets and thymic output in juvenile MG patients.
- To assess the clinical occurrence of autoimmune disorders, malignancies, and infections post-thymectomy.
Main Methods:
- Retrospective cohort study of 47 juvenile MG patients (onset <19 years).
- 32 patients underwent thymectomy; 15 did not.
- Analysis of T cell subsets (CD4+CD45RA+, CD4+CD45RO+, CD8+CD27+CD28+) and T cell receptor rearrangement excision circles (TRECs) 7-26 years post-thymectomy.
Main Results:
- Thymectomized patients showed fewer naïve helper T cells and more memory helper T cells.
- A significant reduction in naïve cytotoxic T cells was observed.
- Reduced TRECs and recent thymic emigrants (RTE) indicated diminished thymic output.
- No increased frequency of malignancies or infections was found.
Conclusions:
- Thymectomy in juvenile MG patients is associated with indicators of premature immune system aging.
- Long-term clinical consequences, such as increased infections or malignancies, were not verified in this cohort.
Abstract:
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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