論文種別 | 総説 |
言語種別 | 英語 |
査読の有無 | その他(不明) |
表題 | 'Can we cure IgG4-related diseases?'. |
掲載誌名 | 正式名:Current opinion in immunology 略 称:Curr Opin Immunol ISSNコード:18790372/09527915 |
掲載区分 | 国外 |
巻・号・頁 | 95,pp.102564 |
著者・共著者 | Kazuichi Okazaki, Tsukasa Ikeura, Kazushige Uchida |
発行年月 | 2025/08 |
概要 | IgG4-related disease (IgG4-RD), recognized as a novel clinical entity, is a rare, chronic, immune-mediated systemic fibroinflammatory disorder of unknown origin with either synchronous or metachronous multi-organ involvement. Although the pathogenic mechanism remains unclear, possible multipathogenic factors such as genetic backgrounds, disease-specific or related antigens, and abnormal innate or adaptive immunity may be involved. Many immunocytes, including neutrophil extracellular trap, M2 macrophage, plasmablast, B cells, and T-cells (Th2-CD4+T, follicular helper T cells, and CD4+SLAMF7+cytotoxic T cells) play important roles in the pathogenesis. Conventional therapies with glucocorticoid or rituximab in combination with/without immunomodulators are recommended in all symptomatic patients with active IgG4-RD. Because of a few of randomized clinical trials, the comprehensive management for IgG4-RD has not been established yet. Targeted treatment approaches against the plasmablast to B cell lineage and the CD4+SLAMF7+cytotoxic T cell seem to be promising for the future-directed treatment. |
DOI | 10.1016/j.coi.2025.102564 |
PMID | 40398200 |