Choremi-Papadopoulou H, Panagiotou N, Samouilidou E, Kontopidou F, Viglis V, Antoniadou A, Kosmidis J, Kordossis T
Immunology Department, Laiko General Hospital, Athens, Greece.
Clin Exp Immunol. 2000 Mar;119(3):499-506. doi: 10.1046/j.1365-2249.2000.01153.x.
In a prospective study of 152 HIV-1 patients (with and without progression to AIDS) we examined CD28 MoAb costimulation and CD3 MoAb response using whole blood culture at baseline and up to either the time of AIDS diagnosis or the end of the observation period. CD28 antigen expression on both CD4+ and CD8+ T lymphocytes was also studied in both groups of patients. In patients who progressed to AIDS, CD28 MoAb costimulation was found to be decreased. Univariate time-dependent analysis showed that decreases in (i) absolute numbers of either CD4+, CD4+CD28+, CD8+CD28+ T cells, (ii) CD28 MoAb costimulation, and (iii) CD3 MoAb response, and an increase in CD8+CD28- %, are significant predictors for progression to AIDS. In addition, multivariate time-dependent analysis demonstrated that a decrease in CD28 MoAb costimulation (but not a decrease in CD3 MoAb response) was predictive for progression to AIDS, as were decreases in the percentage of CD4+ T cells and the absolute number of CD4+CD28+ T cells. Thus, CD28 MoAb costimulation can be considered a useful assay for monitoring HIV-1 infection. Furthermore, apart from the early increase in the percentage of CD8+CD28- T cells and an increase in the percentage of CD28- on CD8+ T cells in both groups of patients at baseline compared with normal controls, a negative correlation was found to exist between the percentages of CD4+ or CD4+CD28+ T cells and the percentage of CD8+CD28- T cells; this suggests that these cells are probably mutually regulated.
在一项针对152名HIV-1患者(包括已进展为艾滋病和未进展为艾滋病的患者)的前瞻性研究中,我们在基线时以及直至艾滋病诊断时或观察期结束时,使用全血培养法检测了CD28单克隆抗体共刺激和CD3单克隆抗体反应。同时还研究了两组患者中CD4+和CD8+ T淋巴细胞上CD28抗原的表达情况。在进展为艾滋病的患者中,发现CD28单克隆抗体共刺激降低。单变量时间依赖性分析显示,(i)CD4+、CD4+CD28+、CD8+CD28+ T细胞的绝对数量减少,(ii)CD28单克隆抗体共刺激降低,(iii)CD3单克隆抗体反应降低,以及CD8+CD28- %增加,是进展为艾滋病的显著预测指标。此外,多变量时间依赖性分析表明,CD28单克隆抗体共刺激降低(而非CD3单克隆抗体反应降低)是进展为艾滋病的预测指标,CD4+ T细胞百分比降低和CD4+CD28+ T细胞绝对数量减少也是如此。因此,CD28单克隆抗体共刺激可被视为监测HIV-1感染的一种有用检测方法。此外,与正常对照组相比,在基线时两组患者中CD8+CD28- T细胞百分比早期增加以及CD8+ T细胞上CD28-百分比增加,而且发现CD4+或CD4+CD28+ T细胞百分比与CD8+CD28- T细胞百分比之间存在负相关;这表明这些细胞可能相互调节。