Yoshikawa N, Morita T, Arreaza G, Resetkova E, Mukuta T, Volpé R
Department of Medicine, Wellesley Hospital, University of Toronto, Ontario.
Clin Invest Med. 1995 Apr;18(2):91-8.
We have investigated the effects of interleukin-2 (IL-2) on the activation of suppressor T lymphocytes in autoimmune thyroid disease (AITD), with insulin-dependent diabetes mellitus (IDDM) as an autoimmune disease control; this was accomplished by measuring the expression of major histocompatibility complex class II (HLA-DR), CD25 (IL-2 alpha receptor (R)), and IL-2 beta R expression on their surfaces by flow cytometric analysis. Peripheral blood mononuclear cells (PBMC), obtained from 10 patients with Graves' disease (GD), 11 with Hashimoto's thyroiditis (HT), 9 with insulin-dependent diabetes mellitus (IDDM), and 10 normal persons (N), were cultured for 7 d in the presence or absence of IL-2 at a final concentration of 50 U/mL. CD8+ cells were isolated from cultured PBMC with immunomagnetic beads, and were stained with fluorescent-conjugated monoclonal antibodies (anti-CD11b, anti-IL-2 alpha R, anti-IL-2 beta R, and anti-HLA-DR); the activation of CD8+CD11b+ ("suppressor") T cells (Ts) by IL-2 was then analyzed on a flow cytometer. In the absence of IL-2, i.e., in the autologous mixed lymphocyte reaction (AMLR), Ts from patients with GD, HT, and IDDM showed significantly lower activation as compared to N when analyzed by HLA-DR expression, but were not significantly different when IL-2R expression was measured. We determined the Stimulation Index (SI) of the activation of T lymphocytes by IL-2 for comparison between N and patients. With stimulation of 50 U/mL of IL-2, SI of HLA-DR+ Ts was significantly (p < 0.05 to 0.01) lower in GD, HT, and IDDM as compared with N.(ABSTRACT TRUNCATED AT 250 WORDS)
我们以胰岛素依赖型糖尿病(IDDM)作为自身免疫性疾病对照,研究了白细胞介素-2(IL-2)对自身免疫性甲状腺疾病(AITD)中抑制性T淋巴细胞激活的影响;这是通过流式细胞术分析测量其表面主要组织相容性复合体II类(HLA-DR)、CD25(IL-2α受体(R))和IL-2βR的表达来实现的。从10例格雷夫斯病(GD)患者、11例桥本甲状腺炎(HT)患者、9例胰岛素依赖型糖尿病(IDDM)患者和10名正常人(N)获取外周血单个核细胞(PBMC),在终浓度为50 U/mL的IL-2存在或不存在的情况下培养7天。用免疫磁珠从培养的PBMC中分离出CD8 +细胞,并用荧光偶联单克隆抗体(抗CD11b、抗IL-2αR、抗IL-2βR和抗HLA-DR)进行染色;然后在流式细胞仪上分析IL-2对CD8 + CD11b +(“抑制性”)T细胞(Ts)的激活情况。在不存在IL-2的情况下,即自体混合淋巴细胞反应(AMLR)中,通过HLA-DR表达分析时,GD、HT和IDDM患者的Ts与N相比显示出明显较低的激活,但在测量IL-2R表达时无显著差异。我们确定了IL-2激活T淋巴细胞的刺激指数(SI)以比较N和患者。在50 U/mL IL-2刺激下,与N相比,GD、HT和IDDM中HLA-DR + Ts的SI显著(p < 0.05至0.01)降低。(摘要截短于250字)