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1.
Tohoku J Exp Med ; 262(1): 29-31, 2024 Jan 23.
Article in English | MEDLINE | ID: mdl-37967941

ABSTRACT

Juvenile myasthenia gravis (JMG) exhibits a more favorable response to glucocorticoids and has a better prognosis than adult myasthenia gravis. However, no established treatment exists for refractory JMG. Although thymectomy has been performed in several patients with refractory systemic JMG, there are few detailed clinical descriptions of patients who underwent thymectomy. Here, we present the case of a 10-year-old boy with refractory systemic JMG who was successfully treated with thymectomy. The patient developed symptoms, including dysphagia, malaise, diurnal ptosis, and weakness in the trunk muscles, and he was diagnosed with generalized JMG. Despite undergoing various treatments, including steroids, tacrolimus, steroid pulse therapy, intravenous immunoglobulin, azathioprine (AZT), and rituximab, his symptoms did not improve. Therefore, he underwent a thoracoscopic thymectomy 24 months after disease onset. Thymectomy led to remission, as demonstrated by a significant reduction in the quantitative myasthenia gravis score and anti-acetylcholine receptor antibody levels, which persisted for 43 months after surgery. Our case demonstrates the effectiveness of thymectomy in systemic JMG patients with positive anti-acetylcholine receptor antibodies, despite therapeutic failure with AZT and rituximab, within 2 years of disease onset.


Subject(s)
Myasthenia Gravis , Thymectomy , Child , Humans , Male , Autoantibodies , Disease Progression , Glucocorticoids/therapeutic use , Myasthenia Gravis/drug therapy , Myasthenia Gravis/surgery , Rituximab , Treatment Outcome
2.
Commun Biol ; 4(1): 285, 2021 03 05.
Article in English | MEDLINE | ID: mdl-33674689

ABSTRACT

In complex structures such as flowers, organ-organ interactions are critical for morphogenesis. The corolla plays a central role in attracting pollinators: thus, its proper development is important in nature, agriculture, and horticulture. Although the intraorgan mechanism of corolla development has been studied, the importance of organ-organ interactions during development remains unknown. Here, using corolla mutants of morning glory described approximately 200 years ago, we show that glandular secretory trichomes (GSTs) regulate floral organ interactions needed for corolla morphogenesis. Defects in GST development in perianth organs result in folding of the corolla tube, and release of mechanical stress by sepal removal restores corolla elongation. Computational modeling shows that the folding occurs because of buckling caused by mechanical stress from friction at the distal side of the corolla. Our results suggest a novel function of GSTs in regulating the physical interaction of floral organs for macroscopic morphogenesis of the corolla.


Subject(s)
Flowers/growth & development , Ipomoea nil/growth & development , Plant Development , Plants, Genetically Modified/growth & development , Trichomes/growth & development , Computer Simulation , Flowers/genetics , Friction , Ipomoea nil/genetics , Models, Biological , Mutation , Plants, Genetically Modified/genetics , Stress, Mechanical , Trichomes/genetics
3.
Front Immunol ; 12: 784901, 2021.
Article in English | MEDLINE | ID: mdl-35087518

ABSTRACT

IKAROS and CTLA4 deficiencies are inborn errors of immunity and show similar clinical phenotypes, including hypogammaglobulinemia and autoimmune diseases (ADs). However, the differences in clinical features and pathogenesis of these are not fully understood. Therefore, we performed systematic literature reviews for IKAROS and CTLA4 deficiencies. The reviews suggested that patients with IKAROS deficiency develop AD earlier than hypogammaglobulinemia. However, no study assessed the detailed changes in clinical manifestations over time; this was likely due to the cross-sectional nature of the studies. Therefore, we conducted a retrospective longitudinal study on IKAROS and CTLA4 deficiencies in our cohort to evaluate the clinical course over time. In patients with IKAROS deficiency, AD and hypogammaglobulinemia often develop in that order, and AD often resolves before the onset of hypogammaglobulinemia; these observations were not found in patients with CTLA4 deficiency. Understanding this difference in the clinical course helps in the clinical management of both. Furthermore, our results suggest B- and T-cell-mediated ADs in patients with IKAROS and CTLA4 deficiencies, respectively.


Subject(s)
CTLA-4 Antigen/deficiency , Ikaros Transcription Factor/deficiency , Metabolism, Inborn Errors , Autoimmune Diseases , Humans , Longitudinal Studies , Primary Immunodeficiency Diseases , Retrospective Studies
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