CD40配体(CD154)在人类免疫缺陷病毒感染儿童中的异常表达

M. O'gorman, B. Duchateau, M. Paniagua, J. Hunt, Nicolas Bensen, R. Yogev
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引用次数: 19

摘要

CD40配体(CD154)主要在活化的cd4阳性T细胞上表达,是一种共刺激分子,参与b细胞增殖、生发中心形成和免疫球蛋白类转换。由于b细胞异常(包括高γ球蛋白血症和异常抗体特异性免疫反应)在儿童人类免疫缺陷病毒(HIV)感染过程中很突出,并且发生在早期,因此我们测量了HIV感染儿童和HIV阳性母亲所生的未感染儿童中CD154在CD3+ CD8−(T辅助细胞)上的基线水平和诱导表达水平。在体外活化的CD154+ T辅助细胞百分比和每T辅助细胞表达的CD154水平(平均荧光通道[MFC])在hiv感染儿童中显著低于未感染对照组(分别为77%±3%对89%±1% [P < 0.002], 261±174对415±130 MFC [P < 0.03])。在hiv感染组中,静止T辅助细胞上表达的CD154水平与对照组中观察到的水平没有显著差异。在hiv感染儿童中,激活T辅助细胞上的CD154水平与免疫缺陷水平相关,通过CD4 T细胞水平评估(相关系数[r] = 0.707,P = 0.003),但与病毒载量或这组hiv感染儿童中测量的任何血清免疫球蛋白浓度无关。然而,T辅助细胞上表达的CD154的基线水平确实与血清中免疫球蛋白A的浓度相关。我们得出结论,hiv感染儿童的CD154表达调节受损,这可能导致普遍观察到的免疫失调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abnormal CD40 Ligand (CD154) Expression in Human Immunodeficiency Virus-Infected Children
ABSTRACT The CD40 ligand (CD154), expressed primarily on activated CD4-positive T cells, is a costimulatory molecule involved in B-cell proliferation, germinal center formation, and immunoglobulin class switching. Since B-cell abnormalities including hypergammaglobulinemia and abnormal antibody-specific immune responses are prominent and occur early during the course of pediatric human immunodeficiency virus (HIV) infection, we measured the baseline levels and the induced levels of expression of CD154 on CD3+ CD8− (T helper cells) in HIV-infected children and uninfected children born to HIV-positive mothers. The percentage of CD154+ T helper cells activated in vitro and the level of CD154 expressed per T helper cell (mean fluorescent channel [MFC]) were significantly lower in the HIV-infected children than in the uninfected control group (77% ± 3% versus 89% ± 1%, respectively [P < 0.002], and 261 ± 174 versus 415 ± 130 MFC, respectively [P < 0.03]). The levels of CD154 expressed on resting T helper cells in the HIV-infected group were not significantly different from the levels observed in the control group. In the HIV-infected children, the level of CD154 on activated T helper cells correlated with the level of immunodeficiency, as assessed by the CD4 T-cell levels (correlation coefficient [r] = 0.707,P = 0.003), but did not correlate with the viral load or with any of the serum immunoglobulin concentrations measured in this group of HIV-infected children. The baseline level of CD154 expressed on T helper cells did, however, correlate with the concentration of immunoglobulin A in serum. We conclude that HIV-infected children have impaired regulation of CD154 expression which may contribute to the immune dysregulation commonly observed.
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