Department of Rheumatology and Immunology, Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
Front Immunol. 2022 Jul 28;13:940581. doi: 10.3389/fimmu.2022.940581. eCollection 2022.
Studies have confirmed the involvement of a variety of lymphocyte subsets, including type 2 helper T lymphocytes (Th2) and IgG4 B lymphocytes, in the pathogenesis of IgG4-related disease (IgG4-RD). Those lymphocytes contribute to the major pathogenetic features of IgG4-RD. However, they are not the only cellular components in the immunoinflammatory environment of this mysterious disease entity. Recent studies have suggested that various non-lymphocytic components, including macrophages and fibroblasts, may also play an important role in the pathogenetic process of IgG4-RD in terms of contributing to the chronic and complex progress of the disease. Therefore, the potential role of non-lymphocyte in the pathogenesis of IgG4-RD is worth discussing.
研究已经证实多种淋巴细胞亚群的参与,包括 2 型辅助 T 淋巴细胞(Th2)和 IgG4B 淋巴细胞,在 IgG4 相关疾病(IgG4-RD)的发病机制中。这些淋巴细胞有助于 IgG4-RD 的主要发病特征。然而,它们并不是这种神秘疾病实体免疫炎症环境中的唯一细胞成分。最近的研究表明,各种非淋巴细胞成分,包括巨噬细胞和成纤维细胞,也可能在 IgG4-RD 的发病过程中发挥重要作用,有助于疾病的慢性和复杂进展。因此,非淋巴细胞在 IgG4-RD 发病机制中的潜在作用值得探讨。