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严重再生障碍性贫血中T淋巴细胞对膜结合型flt3配体的慢性过表达。

Chronic overexpression of membrane-bound flt3 ligand by T lymphocytes in severe aplastic anaemia.

作者信息

Pfister O, Chklovskaia E, Jansen W, Mészáros K, Nissen C, Rahner C, Hurwitz N, Bogatcheva N, Lyman S D, Wodnar-Filipowicz A

机构信息

Department of Research, University Hospital Basle, Switzerland.

出版信息

Br J Haematol. 2000 Apr;109(1):211-20. doi: 10.1046/j.1365-2141.2000.02008.x.

Abstract

Aplastic anaemia (AA) is an immune-mediated bone marrow failure associated with high serum levels of flt3 ligand (FL). We examined expression of the membrane-bound isoform of FL in peripheral blood and bone marrow cells from AA patients at diagnosis (n = 16) and after immunosuppressive (IS) treatment (n = 36). Flow cytometry demonstrated strongly increased FL levels on the cell surface of T lymphocytes in AA relative to normal controls (P < 0.0001). T-cell-specific expression of membrane-bound FL was confirmed by confocal microscopy. FL mRNA and total cellular FL protein levels were increased about threefold. Overexpression of FL in AA was observed for up to 20 years after IS treatment. FL levels correlated inversely with CD34+ cell numbers and the colony-forming ability of AA bone marrow (R = -0.68 and -0.85 respectively). Histological examination of spleen specimens and bone marrow biopsies gave no evidence of degeneration or fibrosis due to prolonged exposure to high FL. Levels of membrane-bound FL were not increased in autoimmune diseases (n = 23), including rheumatoid arthritis and lupus erythematosus, nor in graft-versus-host disease (n = 8). Chronic overexpression of FL on the surface of T lymphocytes in AA, but not in other T-cell-mediated disorders, suggests that membrane-bound FL plays a role in cell-cell interactions in bone marrow failure and may be important for long-term haemopoietic recovery.

摘要

再生障碍性贫血(AA)是一种与血清中高水平的fms样酪氨酸激酶3配体(FL)相关的免疫介导的骨髓衰竭。我们检测了初诊时(n = 16)和免疫抑制(IS)治疗后(n = 36)的AA患者外周血和骨髓细胞中FL膜结合异构体的表达。流式细胞术显示,与正常对照相比,AA患者T淋巴细胞表面的FL水平显著升高(P < 0.0001)。共聚焦显微镜证实了膜结合FL的T细胞特异性表达。FL mRNA和细胞总FL蛋白水平增加了约三倍。IS治疗后长达20年都观察到AA中FL的过表达。FL水平与AA骨髓中CD34 +细胞数量和集落形成能力呈负相关(分别为R = -0.68和-0.85)。脾脏标本和骨髓活检的组织学检查未发现因长期暴露于高FL而导致的变性或纤维化证据。在自身免疫性疾病(n = 23),包括类风湿性关节炎和红斑狼疮,以及移植物抗宿主病(n = 8)中,膜结合FL水平并未升高。AA中T淋巴细胞表面FL的慢性过表达,而非其他T细胞介导的疾病,表明膜结合FL在骨髓衰竭的细胞间相互作用中起作用,并且可能对长期造血恢复很重要。

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