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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。

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.

作者信息

Sakane T, Takada S, Suzuki N, Tsuchida T, Murakawa Y, Ueda Y

出版信息

J Immunol. 1986 Dec 15;137(12):3809-13.

PMID:2946769
Abstract

Concanavalin A (Con A)-activated T lymphocytes from patients with active, but not inactive, systemic lupus erythematosus (SLE) failed to express normal suppressor activity, regardless of the phenotype of CD4+ or CD8+. Con A-activated CD4+ or CD8+ T lymphocytes from the SLE patients and from normal controls were further separated into two populations, using the autologous erythrocyte rosette technique. One population very rich in cells capable of forming rosettes with autologous erythrocytes from the active patients showed the same degree of suppressor activity, as did that from normal controls; the CD4+ or CD8+ population poor in autorosetting cells derived from Con A-activated T lymphocytes from both the controls and patients did not express suppressor activity. Moreover, when autorosetting T cells from the active patients and nonrosetting cells from the same patients were mixed at a normal ratio (4:6), normal suppressor activity could be restored. It was notable that the frequency of autorosette-forming cells was markedly reduced in the Con A-activated T lymphocytes from the active, but not inactive, SLE patients, regardless of the phenotype of CD4+ or CD8+. These findings indicate the presence of a normally functioning suppressor T cell population in patients with active SLE. It seems that the lack of suppressor T cell function in patients with active SLE is due to the dilution of a few normal suppressor T cells by large numbers of nonsuppressor T lymphocytes.

摘要

伴刀豆球蛋白A(Con A)激活的、来自活动期而非非活动期系统性红斑狼疮(SLE)患者的T淋巴细胞,无论其CD4⁺或CD8⁺表型如何,均不能表达正常的抑制活性。利用自体红细胞花环技术,将来自SLE患者和正常对照的Con A激活的CD4⁺或CD8⁺T淋巴细胞进一步分为两个群体。一个群体富含能够与活动期患者的自体红细胞形成花环的细胞,其显示出与正常对照相同程度的抑制活性;来自对照和患者的Con A激活的T淋巴细胞中,自体花环形成细胞较少的CD4⁺或CD8⁺群体不表达抑制活性。此外,当将活动期患者的自体花环形成T细胞与同一患者的非花环形成细胞以正常比例(4:6)混合时,可恢复正常的抑制活性。值得注意的是,无论CD4⁺或CD8⁺表型如何,来自活动期而非非活动期SLE患者的Con A激活的T淋巴细胞中,自体花环形成细胞的频率均显著降低。这些发现表明活动期SLE患者存在功能正常的抑制性T细胞群体。似乎活动期SLE患者抑制性T细胞功能的缺乏是由于少数正常抑制性T细胞被大量非抑制性T淋巴细胞稀释所致。

相似文献

1
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.
2
Functional heterogeneities among concanavalin A-activated OKT4+ and OKT8+ cells by using autologous erythrocyte rosette technique.运用自体红细胞玫瑰花结技术检测伴刀豆球蛋白A激活的OKT4 +和OKT8 +细胞之间的功能异质性。
J Clin Invest. 1983 Dec;72(6):2060-71. doi: 10.1172/JCI111171.
3
Studies of immune functions of patients with systemic lupus erythematosus. Complement-dependent immunoglobulin M anti-thymus-derived cell antibodies preferentially inactivate suppressor cells.系统性红斑狼疮患者免疫功能的研究。补体依赖性免疫球蛋白M抗胸腺细胞抗体优先使抑制细胞失活。
J Clin Invest. 1979 May;63(5):954-65. doi: 10.1172/JCI109396.
4
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.
5
Loss of suppressor T-lymphocyte function in patients with systemic lupus erythematosus (SLE).系统性红斑狼疮(SLE)患者中抑制性T淋巴细胞功能丧失。
Clin Exp Immunol. 1978 Apr;32(1):125-33.
6
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.
7
A defect in the suppressor circuits among OKT4+ cell populations in patients with systemic lupus erythematosus occurs independently of a defect in the OKT8+ suppressor T cell function.系统性红斑狼疮患者OKT4 +细胞群体中抑制回路的缺陷独立于OKT8 +抑制性T细胞功能的缺陷而发生。
J Immunol. 1983 Aug;131(2):753-61.
8
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.
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
Con A suppressor cell assay: a further characterization.刀豆球蛋白A抑制细胞试验:进一步的特性研究
J Clin Lab Immunol. 1983 Mar;10(3):159-63.

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