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类风湿关节炎患者来源的干细胞样记忆 T 细胞的促炎特征。

Proinflammatory Features of Stem Cell-like Memory T Cells from Human Patients with Rheumatoid Arthritis.

机构信息

Graduate Course of Translational Medicine (Immunology), Seoul National University College of Medicine, Seoul, Korea.

Division of Rheumatology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.

出版信息

J Immunol. 2021 Jul 15;207(2):381-388. doi: 10.4049/jimmunol.2000814. Epub 2021 Jun 23.

Abstract

Stem cell-like memory T (Tscm) cells are a subset of memory T cells that have characteristics of stem cells. The characteristics of Tscm cells in patients with rheumatoid arthritis (RA) are not well known. The percentage of CD4 and CD8 Tscm cells in PBMCs and synovial fluid mononuclear cells was measured. After confirming the stem cell nature of Tscm cells, we examined their pathogenicity in RA patients and healthy controls (HCs) by assessing T cell activation markers and cytokine secretion after stimulation with anti-CD3/CD28 beads and/or IL-6. Finally, RNA transcriptome patterns in Tscm cells from RA patients were compared with those in HCs. In this study, the percentage of CD4 and CD8 Tscm cells in total T cells was significantly higher in RA patients than in HCs. Tscm cells self-proliferated and differentiated into memory and effector T cell subsets when stimulated. Compared with Tscm cells from HCs, Tscm cells from RA patients were more easily activated by anti-CD3/CD28 beads augmented by IL-6. Transcriptome analyses revealed that Tscm cells from RA patients showed a pattern distinct from those in HCs; RA-specific transcriptome patterns were not completely resolved in RA patients in complete clinical remission. In conclusion, Tscm cells from RA patients show a transcriptionally distinct pattern and are easily activated to produce inflammatory cytokines when stimulated by TCRs in the presence of IL-6. Tscm cells can be a continuous source of pathogenicity in RA.

摘要

干细胞样记忆 T(Tscm)细胞是记忆 T 细胞的一个亚群,具有干细胞的特征。类风湿关节炎(RA)患者 Tscm 细胞的特征尚不清楚。测量了 PBMC 和滑液单核细胞中 CD4 和 CD8 Tscm 细胞的百分比。在确认 Tscm 细胞的干细胞特性后,我们通过评估抗 CD3/CD28 珠和/或 IL-6 刺激后 T 细胞激活标志物和细胞因子分泌,在 RA 患者和健康对照(HC)中检查了它们的致病性。最后,比较了 RA 患者和 HCs 的 Tscm 细胞中的 RNA 转录组模式。在这项研究中,RA 患者总 T 细胞中 CD4 和 CD8 Tscm 细胞的百分比明显高于 HCs。Tscm 细胞在受到刺激时会自我增殖并分化为记忆和效应 T 细胞亚群。与 HCs 的 Tscm 细胞相比,RA 患者的 Tscm 细胞在由 IL-6 增强的抗 CD3/CD28 珠刺激下更容易被激活。转录组分析显示,RA 患者的 Tscm 细胞表现出与 HCs 不同的模式;在完全临床缓解的 RA 患者中,RA 特异性转录组模式并未完全解决。总之,RA 患者的 Tscm 细胞表现出明显不同的转录模式,并且在存在 IL-6 的情况下,TCR 刺激下很容易产生炎症细胞因子。Tscm 细胞可能是 RA 发病机制的持续来源。

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