Publications by authors named "Yumika Isozaki"

Article Synopsis
  • Dysregulation of apoptosis via the Fas-Fas ligand pathway is linked to autoimmune diseases, prompting a study of autoantibodies against the Fas molecule in patients.
  • Autoantibodies against Fas were detected in patients with silicosis, systemic lupus erythematosus (SLE), and systemic sclerosis (SSc), with weaker presence in healthy individuals, indicating a potential biomarker for these conditions.
  • Epitope mapping revealed several key amino acid residues in the Fas protein that may affect its function, with implications for how anti-Fas autoantibodies could influence disease progression and cell growth.
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We reported previously the autoantibodies directed to caspase-8 among patients with silicosis, systemic sclerosis (SSc) and systemic lupus erythematosus (SLE) , and in healthy individuals. In this study, we analyzed the correlation between anti-caspase-8 autoantibody responses and HLA class II alleles in silicosis patients. The frequencies of HLA-DRB1*0406 were significantly higher in antibody positive patients (16.

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Objectives: The aim of this study was to detect anti-topoisomerase I (anti-topo I) autoantibodies, which are known to be limited in systemic sclerosis patients, in silicosis patients with no clinical symptoms of autoimmune disease.

Methods: Serum anti-topo I autoantibodies were detected using ELISA. Differences in clinical parameters between patients with and without anti-topo I autoantibodies were analyzed.

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Recently, it was disclosed that all-trans retinoic acid (ATRA) inhibits myeloma cell growth by downregulating the interleukin 6 (IL-6)/IL-6 receptor (IL-6R) auto/paracrine loop, and upregulating p21/Cip1 cyclin-dependent kinase inhibitor (CDK-I), thereby inducing apoptosis with a decrease in Bcl-2 protein expression. To elucidate and generalize the effects of ATRA on the proliferation and cellular biology of myeloma cells, 12 human myeloma cell lines established in our laboratory were utilized. Two out of the 12 lines showed enhanced growth on supplementation of ATRA and were characterized by IL-10 production, downregulation of membrane Fas and reduced upregulation of p21/Cip1 CDK-I message.

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