Alexander G J, Nouri-Aria K T, Eddleston A L, Williams R
Lancet. 1983 Jun 11;1(8337):1291-3. doi: 10.1016/s0140-6736(83)92410-8.
75 patients with various chronic liver diseases were investigated by simultaneous assay of suppressor-cell function and enumeration of suppressor T cells by monoclonal antibody. In chronic active hepatitis and primary biliary cirrhosis, substantial defects in suppressor-cell function were associated with negligible alterations in the proportions of suppressor cells. Defective suppressor-cell function was also evident in most patients with HBsAg-positive liver disease and in some with alcoholic liver disease. While the expected relations between suppressor-cell function and the proportions of helper or suppressor cells and the helper/suppressor ratio were apparent in alcoholic liver disease, the results in the HBsAg-positive, HBeAg-positive patients were in direct contrast. This apparent anomaly may reflect functional heterogeneity of the lymphocyte population detected by the monoclonal antibody OKT8, which identifies suppressor and cytotoxic cells. This study demonstrates that in the absence of simultaneous measurement of function, enumeration of T-cell subsets with monoclonal antibodies is an inadequate assessment of immunoregulatory balance.
通过单克隆抗体同时检测抑制细胞功能和计数抑制性T细胞,对75例各种慢性肝病患者进行了研究。在慢性活动性肝炎和原发性胆汁性肝硬化中,抑制细胞功能的显著缺陷与抑制细胞比例的微小改变相关。在大多数HBsAg阳性肝病患者和一些酒精性肝病患者中,抑制细胞功能缺陷也很明显。虽然在酒精性肝病中,抑制细胞功能与辅助性或抑制性细胞比例及辅助/抑制细胞比值之间的预期关系很明显,但HBsAg阳性、HBeAg阳性患者的结果却截然相反。这种明显的异常可能反映了通过单克隆抗体OKT8检测到的淋巴细胞群体的功能异质性,OKT8可识别抑制性和细胞毒性细胞。本研究表明,在没有同时测量功能的情况下,用单克隆抗体计数T细胞亚群不足以评估免疫调节平衡。