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[作为系统性红斑狼疮中T-T细胞相互作用缺陷表现的与同种异体淋巴细胞增殖相关的抑制因子活性亢进]

[Suppressor hyperactivity in relation to allogeneic lymphocyte proliferation as a manifestation of T- T-cell interaction defects in systemic lupus erythematosus].

作者信息

Stenina M A, Potapova A A, Biriukov A V, Skripnik A Iu, Cheredeev A H

出版信息

Biull Eksp Biol Med. 1986 Aug;102(8):215-7.

PMID:2874848
Abstract

Phytohemagglutinin-stimulated lymphocyte proliferation by con A-induced immunoregulatory cells has been estimated in patients with active systemic lupus erythematosus (SLE) treated with prednisolone. Using the combination of normal immunoregulatory cells and proliferating target cells from normal donors with immunoregulatory cells and target cells from SLE patients, it was shown that the response to immunoregulatory cells in target cells of SLE patients was impaired. This is confirmed by a slight inhibition of SLE target cell proliferation and the activating effect of immunoregulatory cells on the proliferation of "sick" targets. The data give evidence of impaired T-T-cell interaction that may be a possible mechanism of immunoregulatory defects in SLE. These disturbances can, probably, cause hyperreactivity of suppressor cells affecting normal lymphocyte proliferation. It was shown that theophylline was useful for the correction of these disorders.

摘要

在接受泼尼松龙治疗的活动性系统性红斑狼疮(SLE)患者中,已对伴刀豆球蛋白A诱导的免疫调节细胞刺激的植物血凝素刺激淋巴细胞增殖进行了评估。使用来自正常供体的正常免疫调节细胞与增殖靶细胞以及来自SLE患者的免疫调节细胞与靶细胞的组合,结果显示SLE患者靶细胞中对免疫调节细胞的反应受损。SLE靶细胞增殖的轻微抑制以及免疫调节细胞对“病态”靶细胞增殖的激活作用证实了这一点。这些数据证明了T - T细胞相互作用受损,这可能是SLE免疫调节缺陷的一种可能机制。这些紊乱可能会导致抑制细胞的反应过度,从而影响正常淋巴细胞增殖。结果表明,茶碱对纠正这些紊乱是有用的。

相似文献

1
[Suppressor hyperactivity in relation to allogeneic lymphocyte proliferation as a manifestation of T- T-cell interaction defects in systemic lupus erythematosus].[作为系统性红斑狼疮中T-T细胞相互作用缺陷表现的与同种异体淋巴细胞增殖相关的抑制因子活性亢进]
Biull Eksp Biol Med. 1986 Aug;102(8):215-7.
2
Impaired immunoregulation in systemic lupus erythematosus: defective adenosine-induced suppressor T lymphocyte generation.系统性红斑狼疮中免疫调节受损:腺苷诱导的抑制性T淋巴细胞生成缺陷。
J Immunol. 1983 Apr;130(4):1706-12.
3
Phytohemagglutinin response in systemic lupus erythematosus. Reconstitution experiments using highly purified lymphocyte subpopulations and monocytes.系统性红斑狼疮中的植物血凝素反应。使用高度纯化的淋巴细胞亚群和单核细胞的重建实验。
J Clin Invest. 1977 Sep;60(3):626-38. doi: 10.1172/JCI108814.
4
Deficiencies in suppressor T cell activity seen in patients with active systemic lupus erythematosus are due to the dilution of normally functioning suppressor T cells by nonsuppressor T cells.在活动性系统性红斑狼疮患者中观察到的抑制性T细胞活性缺陷,是由于正常发挥功能的抑制性T细胞被非抑制性T细胞稀释所致。
J Immunol. 1986 Dec 15;137(12):3809-13.
5
Depressed primary in vitro antibody response in untreated systemic lupus erythematosus. T helper cell defect and lack of defective suppressor cell function.未经治疗的系统性红斑狼疮患者体外抗体反应低下。辅助性T细胞缺陷且抑制性细胞功能无缺陷。
J Clin Invest. 1980 Jul;66(1):141-8. doi: 10.1172/JCI109827.
6
Suppressor-cell dysfunction in systemic lupus erythematosus. Cells involved and in vitro correction.系统性红斑狼疮中的抑制细胞功能障碍。涉及的细胞及体外纠正。
J Clin Invest. 1978 Oct;62(4):789-96. doi: 10.1172/JCI109190.
7
[The dysfunction of human peripheral blood dendritic cells on concanavalin A-induced T cell responses in patients with systemic lupus erythematosus].[系统性红斑狼疮患者外周血树突状细胞对伴刀豆球蛋白A诱导的T细胞反应的功能障碍]
Arerugi. 1992 Jun;41(6):693-8.
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Characterization of T lymphocyte subpopulations responsible for deficient interleukin 2 activity in patients with systemic lupus erythematosus.系统性红斑狼疮患者中负责白细胞介素2活性不足的T淋巴细胞亚群的特征分析。
J Immunol. 1985 Jan;134(1):187-95.
9
Suppressor-cell antibody in systemic lupus erythematosus. Possible mechanism for suppressor-cell dysfunction.系统性红斑狼疮中的抑制细胞抗体。抑制细胞功能障碍的可能机制。
J Clin Invest. 1979 Mar;63(3):536-9. doi: 10.1172/JCI109333.
10
Allogeneic suppression of polyclonal immunoglobulin production in normals and patients with systemic lupus erythematosus.正常人和系统性红斑狼疮患者多克隆免疫球蛋白产生的同种异体抑制。
Clin Exp Immunol. 1980 Oct;42(1):27-32.