Peripheral T cell profiling reveals downregulated exhaustion marker and increased diversity in lymphedema post-lymphatic venous anastomosis
Lymphedema is a progressive condition accompanying cellulitis and angiosarcoma, suggesting its association with immune dysfunction. Lymphatic venous anastomosis (LVA) can provide relief from cellulitis and angiosarcoma. However, the immune status of peripheral T cells during lymphedema and post-LVA...
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Veröffentlicht in: | iScience 2023-06, Vol.26 (6), p.106822-106822, Article 106822 |
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Sprache: | eng |
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Zusammenfassung: | Lymphedema is a progressive condition accompanying cellulitis and angiosarcoma, suggesting its association with immune dysfunction. Lymphatic venous anastomosis (LVA) can provide relief from cellulitis and angiosarcoma. However, the immune status of peripheral T cells during lymphedema and post-LVA remains poorly understood. Using peripheral blood T cells from lymphedema, post-LVA, and healthy controls (HCs), we compared the profile of T cell subsets and T cell receptor (TCR) diversity. PD-1+ Tim-3 + expression was downregulated in post-LVA compared with lymphedema. IFN-γ levels in CD4+PD-1+ T cells and IL-17A levels in CD4+ T cells were downregulated in post-LVA compared with lymphedema. TCR diversity was decreased in lymphedema compared with HCs; such TCR skewing was drastically improved in post-LVA. T cells in lymphedema were associated with exhaustion, inflammation, and diminished diversity, which were relieved post-LVA. The results provide insights into the peripheral T cell population in lymphedema and highlight the immune modulatory importance of LVA.
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•We demonstrated the peripheral T cell condition in lymphedema•The influence of lymphatic venous anastomosis on peripheral T cells was elucidated•T cells after lymphatic venous anastomosis demonstrated upregulation of diversity•Our results highlight the importance of LVA apart from its edema-reducing effect
Health sciences; Immunology; Components of the immune system |
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ISSN: | 2589-0042 2589-0042 |
DOI: | 10.1016/j.isci.2023.106822 |