肝细胞癌
医学
细胞毒性T细胞
肝硬化
CD8型
白细胞介素2受体
免疫系统
内科学
CD3型
癌
癌症研究
胃肠病学
T细胞
免疫学
生物
生物化学
体外
作者
C Marafin,Mauro Rinaldi,C. Angonese,G. De Franchis,Mario Plebani,R. Naccarato,Fabio Farinati
出处
期刊:PubMed
日期:1996-12-01
卷期号:28 (9): 493-8
被引量:2
摘要
The immune response in liver cirrhosis and hepatocellular carcinoma is receiving renewed attention in consideration of the possible treatment with biological response modifiers. The aim of this study was to evaluate whether cirrhosis and hepatocellular carcinoma induce any modification in peripheral lymphocyte subsets. Lymphocytes were evaluated (number/percentage) in 61 patients with hepatocellular carcinoma, 35 with cirrhosis and 24 healthy controls. Using flow cytometry, 10 lymphocyte subpopulations were assayed, plus the CD4/CD8 ratio. Results demonstrated no change in the number of lymphocytes; cirrhosis and hepatocellular carcinoma patients had significantly more HLA-DR+ (p = 0.001) and CD3+/HLA-DR+ (activated T) (p = 0.002) and fewer CD3+ (mature T) (p = 0.02) cell than controls; hepatocellular carcinoma patients had significantly more CD3+/CD56+/CD16- (cytotoxic non-MHC restricted T cells) and CD25+ (IL-2 receptor positive cells). If the percentages of all cells with cytotoxic-T activity were pooled, a significant increase (p = 0.03) was seen in hepatocellular carcinoma patients. In conclusion, in contrast to previous data, hepatocellular carcinoma patients reveal an increased number of cytotoxic non-MHC restricted T cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI