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系统性红斑狼疮患者外周血淋巴细胞CD43抗原的研究 被引量:2

Prelim inary Study of Expression of CD43 Antigen on L ym phocytes of Peripheral Blood in Patients with SL E
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摘要 目的 探讨 SL E免疫功能异常的原因。方法 采用免疫荧光双标记 -流式细胞仪检测了 16例活动期 SL E患者外周血淋巴细胞的 CD43抗原。结果  1活动期 SL E患者外周血 CD43抗原阳性淋巴细胞为 6 3.14± 16 .47,低于正常人对照组 86 .6 2± 12 .86 ,有非常显著性差异 (P<0 .0 1) ;2 CD43抗原阳性淋巴细胞数与 SL E疾病活动度呈显著负相关 ,r=-0 .70 2 ,P<0 .0 1;3活动期 SL E患者外周血 CD19+ -CD43+淋巴细胞为 2 .5 5± 1.38,高于对照组 1.32± 0 .92 ,有非常显著性差异 (P<0 .0 1)。结论CD19+ -CD43+淋巴细胞的增多可能与 SL E大量产生抗 DNA自身抗体有关。 Objective To investigate the causes of im m unological disorders in SL E.Methods CD43 antigen on lym phocytes of peripheral blood in 16 cases of active SL E w as detected by im - m unoflourescent double m arker-flow cytom etry.Results The results showed that,(1) the num ber of CD43 antigen positive lym phocytes in peripheral blood of active SL E patients was 6 3.14± 16 .47,w hich w as significantly low er than that of the control group(86 .6 2± 12 .86 ,P<0 .0 1) .(2 ) The number of CD43 antigen positive cells w as negatively correlated to the disease activity of SL E (r=-0 .70 2 ,P<0 .0 1) . (3) The num ber of CD19+ -CD43+ lymphocytes in peripheral blood in active SL E was2 .5 5± 1.38w hich w as significantly higher than that of the control group (1.32± 0 .92 ,P<0 .0 1) .Conclusion The increase of CD19+ -CD43+ lym phocytes may be correlated with the production of anti-DN A autoantibody in SL E.
出处 《中华皮肤科杂志》 CAS CSCD 北大核心 1998年第1期14-15,共2页 Chinese Journal of Dermatology
关键词 系统性红斑狼疮 流式细胞计数 CD43 抗原 L upus erythem atosus,systemic Flowcytom etry CD43
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  • 1张莉,梁再赋,张士发,张恩,李莉,贾秀坤,薛红.SLE患者外周血单一核细胞CD43基因的表达[J].中国麻风皮肤病杂志,2005,21(6):432-434. 被引量:1
  • 2Mangalam AK, Aggarwal A, Naik S, et al. Mechanism of action of disease modifying anti-rheumatic agent, gold sodium thiomalate.Int J Immunopharmacol 2001;6:1165-1172.
  • 3Dragone LL, Barth RK, Sitar KL, et al. Disregulation of leukosialin expression in the B cell lineage of transgenic mice increase splenic B cell number and survival. Proc Natl Acad Sci USA 1995;92:626-630.
  • 4Fanales-Belasio E, Zambmno G, Cavani A, et al. Aautibodies against sialoporin enhance the capacity of dendritic cell to cluster and activate T lymphocytes. J Immunol 1997;159:2203-2211.
  • 5Gallego MD, Aguado E, Kindelan JM, et al. Altered expression of CIM3-hexasaccharide isoform on peripheral T lymphocytes from HIV-infected individuals. AIDS 2001;15:477-481.
  • 6Katsiari CG, Liossis SN, Souliotis VL, et al. Aberrant expression of the costimtdatory molecule CD40 ligand on monocytes from patients with systemic lupus erythematosus. Clin Immunol 2002; 103: 54-62.
  • 7Vassiloponlos D, Kovacs B, Tsokos GC. TCR/CD3 complex-mediated signal transduction pathway in T cells and T cell lines from patients with systemic lupus erythematosus. J Immunol 1995;155:2269-2281.

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