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[人类免疫缺陷病毒感染及机会性感染患者血清辅助性T淋巴细胞(TH)细胞因子变化的临床观察]

[Clinical observation of the changes of serum helper T-lymphocytes (TH) cytokines in patients with HIV-infection and opportunistic infection].

作者信息

Rao He-Ping, Feng Lei, Li Dan, Bader Armin, Wu Nan-Ping

机构信息

Medical Department of Quzhou College, Quzhou, Zhejiang Province 324000, China.

出版信息

Zhonghua Yu Fang Yi Xue Za Zhi. 2007 Jan;41(1):42-5.

Abstract

OBJECTIVE

To observe the changes of serum helper T-Lymphocyte (Th) cytokines at each stage in patients with human immunodeficiency virus (HIV) infection and with opportunistic infection.

METHODS

Seventeen normal subjects were studied as controls. Among the 85 patients with HIV-infection studied, 31 had opportunistic infection. The study was divided into stage A, B, and C according to the standards set forth by The US Centers for Disease Control and Prevention (CDC). 17, 29, and 39 subjects were respectively at stage A, B, and C. The levels of the CD4+ T cells and the CD8+ T cells were measured by flow cytometry (FCM), while the levels of interleukin-2 (IL-2), interferon-gamma (IFN-gamma), interleukin-6 (IL-6), and interleukin-10 (IL-10) were measured using enzyme-linked immunosorbent assay (ELISA). All data were analyzed with statistic software SPSS11.0.

RESULTS

The level of the CD4+ T cells was (361.85 +/- 230.61) 10(6)/L in the experimental group, lower than that of the control group (772.41 +/- 161.56) 10(6)/L (t = 6.992, P < 0. 01). The level of IL-2 was (61.82 +/- 63.59) pg/ml, lower than that of the control group (111.25 +/- 66.14) pg/ml (t = 2.907, P < 0.01). In the experimental group, the level of the CD8+ T cells was 713.36 +/- 317.59 10(6)/L, higher than that of the control group (583.24 +/- 96.28) 10(6)/L (t = 3.127, P < 0.01), the level of IL-10 was (1362.70 +/- 869.49) pg/ml, higher than that of the control group (818.54 +/- 276.22) pg/ml (t = 4.704, P < 0.01), and the level of IL-6 was (1883.14 +/- 1058.61) pg/m, higher than that of the control group [(1208.52 +/-745.36) pg/ml] (t = 2.502, P < 0.05). Along with the progression of the disease, the level of IL-2 in the experimental group was decreasing gradually, reaching (51.72 +/- 62.28) pg/ml at stage C and (69.02 +/- 62.77) pg/ml at stage B, both of which were lower than those of the control group. The levels of IL-6 and IL-10 rose gradually and were (2040.27 +/- 1078.95) pg/ml and (1472.10 +/-982.03 ) pg/ml respectively at stage C, higher than those of the control group. At stage B, the level of IL-10 was (1347.35 +/- 780.95) pg/ml, higher than that of the control group (818.54 +/- 276.22) pg/ml. The level of IL-6 was (2236.24 +/- 1052.42) pg/ml in patients with opportunistic infection, higher than that in those without opportunistic infection (1680.43 +/- 1017.05) pg/ml (t = 2. 395, P < 0. 05).

CONCLUSION

Dynamical measure of the levels of the serum IL-2, IL-6 and IL-10 in patients with HIV infection is a must. Therefore, the progression of AIDS can be controlled by increasing the level of IL-2, decreasing the levels of IL-6 and IL-10, and adjusting the balance of TH1/TH2 cells.

摘要

目的

观察人类免疫缺陷病毒(HIV)感染及合并机会性感染患者各阶段血清辅助性T淋巴细胞(Th)细胞因子的变化。

方法

选取17名正常受试者作为对照。在85例接受研究的HIV感染患者中,31例合并机会性感染。根据美国疾病控制与预防中心(CDC)制定的标准将研究分为A、B、C期。分别有17、29和39名受试者处于A、B、C期。采用流式细胞术(FCM)检测CD4+T细胞和CD8+T细胞水平,采用酶联免疫吸附测定(ELISA)检测白细胞介素-2(IL-2)、干扰素-γ(IFN-γ)、白细胞介素-6(IL-6)和白细胞介素-10(IL-10)水平。所有数据用统计软件SPSS11.0进行分析。

结果

实验组CD4+T细胞水平为(361.85±230.61)×10⁶/L,低于对照组(772.41±161.56)×10⁶/L(t = 6.992,P < 0.01)。IL-2水平为(61.82±63.59)pg/ml,低于对照组(111.25±66.14)pg/ml(t = 2.907,P < 0.01)。实验组CD8+T细胞水平为713.36±317.59×10⁶/L,高于对照组(583.24±96.28)×10⁶/L(t = 3.127,P < 0.01),IL-10水平为(1362.70±869.49)pg/ml,高于对照组(818.54±276.22)pg/ml(t = 4.704,P < 0.01),IL-6水平为(1883.14±1058.61)pg/ml,高于对照组[(1208.52±745.36)pg/ml](t = 2.502,P < 0.05)。随着疾病进展,实验组IL-2水平逐渐下降,C期降至(51.72±62.28)pg/ml,B期降至(69.02±62.77)pg/ml,均低于对照组。IL-6和IL-10水平逐渐升高,C期分别为(2040.27±1078.95)pg/ml和(1472.10±982.03)pg/ml,高于对照组。B期IL-10水平为(1347.35±780.95)pg/ml,高于对照组(818.54±276.22)pg/ml。合并机会性感染患者的IL-6水平为(2236.24±1052.42)pg/ml,高于未合并机会性感染患者(1680.43±1017.05)pg/ml(t = 2.395,P < 0.05)。

结论

必须动态检测HIV感染患者血清IL-2、IL-6和IL-10水平。因此,可通过提高IL-2水平、降低IL-6和IL-10水平以及调整TH1/TH2细胞平衡来控制艾滋病的进展。

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