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系统性红斑狼疮中可溶性自然杀伤细胞细胞毒性因子释放受损。

Impaired release of a soluble natural killer cytotoxic factor in systemic lupus erythematosus.

作者信息

Sibbitt W L, Mathews P M, Bankhurst A D

出版信息

Arthritis Rheum. 1984 Oct;27(10):1095-100. doi: 10.1002/art.1780271003.

Abstract

Disease states characterized by abnormalities in immune regulation often demonstrate concomitant abnormalities in cytotoxicity mediated by natural killer (NK) cells. For example, some patients with systemic lupus erythematosus (SLE) have depressed NK activity despite the presence of normal numbers of effector cell:target cell conjugates. This study was designed to determine if defects in NK cell function were directly related to impaired release of a soluble cytotoxic factor. NK activity of peripheral blood mononuclear cells and large granular lymphocytes was measured using 51Cr-labeled K562 target cells in 4-hour release assays. The SLE patients had significantly decreased NK activity relative to normal controls. However, the number of effector cell:target cell conjugates was not different in SLE patients versus control subjects. The release of a soluble natural killer cytotoxic factor (NKCF) by peripheral blood mononuclear cells was measured by cytotoxicity induced in K562 cells. NKCF was released preferentially by suspensions enriched in NK cells (large granular lymphocytes). At a 1:1 dilution, NKCF release was significantly lower in SLE patients than in controls. The release of NKCF correlated well with NK activity. Thus, this study shows that the defect in NK cell activity in SLE patients may be related to an impairment in release of a soluble cytotoxic factor with specificity for NK cell-sensitive targets.

摘要

以免疫调节异常为特征的疾病状态通常表现出自然杀伤(NK)细胞介导的细胞毒性同时异常。例如,一些系统性红斑狼疮(SLE)患者尽管效应细胞与靶细胞结合物数量正常,但NK活性却降低。本研究旨在确定NK细胞功能缺陷是否与可溶性细胞毒性因子释放受损直接相关。在4小时释放试验中,使用51Cr标记的K562靶细胞测量外周血单个核细胞和大颗粒淋巴细胞的NK活性。与正常对照组相比,SLE患者的NK活性显著降低。然而,SLE患者与对照受试者的效应细胞与靶细胞结合物数量并无差异。通过K562细胞诱导的细胞毒性来测量外周血单个核细胞释放可溶性自然杀伤细胞毒性因子(NKCF)的情况。NKCF优先由富含NK细胞(大颗粒淋巴细胞)的悬液释放。在1:1稀释时,SLE患者的NKCF释放明显低于对照组。NKCF的释放与NK活性密切相关。因此,本研究表明,SLE患者NK细胞活性缺陷可能与对NK细胞敏感靶标具有特异性的可溶性细胞毒性因子释放受损有关。

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