دورية أكاديمية

Similarity and difference between systemic lupus erythematosus and NZB/W F1 mice by multi-omics analysis.

التفاصيل البيبلوغرافية
العنوان: Similarity and difference between systemic lupus erythematosus and NZB/W F1 mice by multi-omics analysis.
المؤلفون: Okuma K; Center for Innovation in Immunoregulation Technology and Therapeutics, Kyoto University Graduate School of Medicine, Kyoto, Japan.; Drug Discovery Research, Astellas Pharma Inc., Tsukuba, Ibaraki, Japan., Oku T; Center for Innovation in Immunoregulation Technology and Therapeutics, Kyoto University Graduate School of Medicine, Kyoto, Japan.; Drug Discovery Research, Astellas Pharma Inc., Tsukuba, Ibaraki, Japan., Sasaki C; Center for Innovation in Immunoregulation Technology and Therapeutics, Kyoto University Graduate School of Medicine, Kyoto, Japan.; Drug Discovery Research, Astellas Pharma Inc., Tsukuba, Ibaraki, Japan., Kitagori K; Center for Innovation in Immunoregulation Technology and Therapeutics, Kyoto University Graduate School of Medicine, Kyoto, Japan.; Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan., Mimori T; Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.; Takeda General Hospital, Kyoto, Japan., Aramori I; Center for Innovation in Immunoregulation Technology and Therapeutics, Kyoto University Graduate School of Medicine, Kyoto, Japan.; Drug Discovery Research, Astellas Pharma Inc., Tsukuba, Ibaraki, Japan., Hirayama Y; Center for Innovation in Immunoregulation Technology and Therapeutics, Kyoto University Graduate School of Medicine, Kyoto, Japan.; Drug Discovery Research, Astellas Pharma Inc., Tsukuba, Ibaraki, Japan., Yoshifuji H; Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
المصدر: Modern rheumatology [Mod Rheumatol] 2024 Feb 26; Vol. 34 (2), pp. 359-368.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 100959226 Publication Model: Print Cited Medium: Internet ISSN: 1439-7609 (Electronic) Linking ISSN: 14397595 NLM ISO Abbreviation: Mod Rheumatol Subsets: MEDLINE
أسماء مطبوعة: Publication: 2021- : Oxford : Oxford University Press
Original Publication: Tokyo, Japan : Spring-Verlag Tokyo, c2000-
مواضيع طبية MeSH: Multiomics* , Lupus Erythematosus, Systemic*/drug therapy, Mice ; Humans ; Animals ; Rabbits ; Mice, Inbred NZB ; T-Lymphocytes/metabolism ; Cytokines/metabolism ; Disease Models, Animal
مستخلص: Objectives: Several animal disease models have been used to understand the mechanisms of systemic lupus erythematosus (SLE); however, the translation of findings from animals to humans has not been sufficiently examined in drug development. To confirm the validity of New Zealand black x New Zealand white (NZB/W) F1 mice as an SLE model, we extensively characterized SLE patients and NZB/W F1 mice by omics analysis.
Methods: Peripheral blood from patients and mice and spleen and lymph node tissue from mice were analysed using cell subset analysis, cytokine panel assays, and transcriptome analysis.
Results: CD4+ effector memory T cells, plasmablasts, and plasma cells were increased in both SLE patients and NZB/W F1 mice. Levels of tumor necrosis factor-α, interferon gamma induced protein-10, and B cell activating factor in plasma were significantly higher in SLE patients and NZB/W F1 mice than in their corresponding controls. Transcriptome analysis revealed an upregulation of genes involved in the interferon signalling pathway and T-cell exhaustion signalling pathway in both SLE patients and the mouse model. In contrast, death receptor signalling genes showed changes in the opposite direction between patients and mice.
Conclusion: NZB/W F1 mice are a generally suitable model of SLE for analysing the pathophysiology and treatment response of T/B cells and monocytes/macrophages and their secreted cytokines.
(© Japan College of Rheumatology 2023. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
فهرسة مساهمة: Keywords: Cytokine; NZB/W F1 mouse; multi-omics; systemic lupus erythematosus; transcriptome
المشرفين على المادة: 0 (Cytokines)
تواريخ الأحداث: Date Created: 20230304 Date Completed: 20240228 Latest Revision: 20240228
رمز التحديث: 20240228
DOI: 10.1093/mr/road024
PMID: 36869711
قاعدة البيانات: MEDLINE
الوصف
تدمد:1439-7609
DOI:10.1093/mr/road024