Kantor T V, Whiteside T L, Friberg D, Buckingham R B, Medsger T A
Department of Medicine, University of Pittsburgh School of Medicine, Pennsylvania.
Arthritis Rheum. 1992 Jun;35(6):694-9. doi: 10.1002/art.1780350615.
To determine the ability of T lymphocytes and natural killer (NK) cells from patients with systemic sclerosis (SSc) to respond to cytokines and to generate immune effector cells.
The numbers and percentages of peripheral blood T and NK cells were examined by 2-color flow cytometry, and NK and lymphokine-activated killer (LAK) cell function were measured in 4-hour 51Cr-release assays, in 34 patients with SSc. The patients were categorized into 3 subgroups: 10 had diffuse cutaneous disease of less than or equal to 3 years disease duration, 11 had diffuse cutaneous SSc of greater than 3 years duration, and 13 had limited cutaneous disease.
Baseline and activated NK and T cell numbers and NK activity were normal in SSc patients. However, mean LAK activity was significantly depressed in all SSc subgroups.
Decreased LAK cell function, despite normal numbers of circulating T and NK cells, indicates that SSc patients have poor ability to produce effector cells in response to interleukin-2.
确定系统性硬化症(SSc)患者的T淋巴细胞和自然杀伤(NK)细胞对细胞因子作出反应并产生免疫效应细胞的能力。
采用双色流式细胞术检测34例SSc患者外周血T细胞和NK细胞的数量及百分比,并在4小时51Cr释放试验中检测NK细胞和淋巴因子激活的杀伤(LAK)细胞功能。患者被分为3个亚组:10例患有病程小于或等于3年的弥漫性皮肤疾病,11例患有病程大于3年的弥漫性皮肤SSc,13例患有局限性皮肤疾病。
SSc患者的基线及活化NK细胞和T细胞数量以及NK活性均正常。然而,所有SSc亚组的平均LAK活性均显著降低。
尽管循环T细胞和NK细胞数量正常,但LAK细胞功能降低表明SSc患者产生白细胞介素-2反应性效应细胞的能力较差。