Lombardo L, Capaldi A, Poccardi G, Vineis P
Department of Gastroenterology, Ospedale Mauriziano U.I., Turin, Italy.
Int J Clin Lab Res. 1995;25(3):153-6. doi: 10.1007/BF02592558.
Immunological disturbances with impairment of immune function and a higher incidence of lymphoproliferative disorders and other malignancies have been described in liver cirrhosis patients. To investigate the pathogenetic mechanism(s) involved in such associated we looked for a possible imbalance in peripheral blood T-lymphocyte subpopulations in patients with liver cirrhosis of differing severity. Immunophenotyping and counts of peripheral blood T-lymphocyte subpopulations were carried out using monoclonal antibodies conjugated with different fluorochromes in 31 consecutive cirrhotic patients and 23 matched healthy volunteers. Univariate and multivariate analyses of lymphocyte phenotype counts were performed and odds ratios were computed. Statistically significant associations, according to both univariate and multivariate analyses, were found between case/control status and mean CD3 and CD4 T-lymphocyte counts (P < 0.0001). A strong correlation was found between the Pugh's index and CD3 and CD4 lymphocyte counts, with a clear reduction of these phenotypes with increasing liver cirrhosis. Median CD3 and CD4 values were 2,283 and 1,329/microliters respectively among controls and 896, 801, and 492/microliters and 515, 514, and 307/microliters, respectively in categories A, B, and C of Pugh's classification. Very high odds ratios were found using the median values of CD3 and CD4 as a threshold. There was a statistically significant decrease for each of the T-cell phenotypes studied (CD2, CD3, CD4, CD8, CD16, CD19, CD20, CD56, CD57) between patients and controls (P < 0.0001). The progressive and severity-related decrease in mean peripheral blood CD3 and CD4 counts in liver cirrhosis suggests a progressive impairment of protective immune function and may be a factor facilitating malignancy in cirrhotic patients.
肝硬化患者存在免疫功能受损的免疫紊乱,且淋巴增殖性疾病和其他恶性肿瘤的发病率较高。为了研究此类关联背后的发病机制,我们在不同严重程度的肝硬化患者中寻找外周血T淋巴细胞亚群可能存在的失衡情况。我们使用与不同荧光染料偶联的单克隆抗体,对31例连续的肝硬化患者和23名匹配的健康志愿者进行外周血T淋巴细胞亚群的免疫表型分析和计数。对淋巴细胞表型计数进行单因素和多因素分析,并计算优势比。根据单因素和多因素分析,病例/对照状态与平均CD3和CD4 T淋巴细胞计数之间存在统计学显著关联(P < 0.0001)。发现Pugh指数与CD3和CD4淋巴细胞计数之间存在强相关性,随着肝硬化程度的增加,这些表型明显减少。在对照组中,CD3和CD4的中位数分别为2,283和1,329/微升,在Pugh分类的A、B和C类中分别为896、801和492/微升以及515、514和307/微升。以CD3和CD4的中位数作为阈值时,发现优势比非常高。患者与对照组之间研究的每种T细胞表型(CD2、CD3、CD4、CD8、CD�16、CD19、CD20、CD56、CD57)均有统计学显著下降(P < 0.0001)。肝硬化患者外周血平均CD3和CD4计数的逐渐下降以及与严重程度相关的下降表明保护性免疫功能逐渐受损,可能是促进肝硬化患者发生恶性肿瘤的一个因素。