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酒精性肝病血清对淋巴细胞转化的抑制作用。

Suppressive effect of alcoholic liver disease sera on lymphocyte transformation.

作者信息

Young G P, Dudley F J, Van Der Weyden M B

出版信息

Gut. 1979 Oct;20(10):833-9. doi: 10.1136/gut.20.10.833.

Abstract

The effect of alcoholic patient sera on in vitro lymphocyte transformation was studied using mitogen-induced uptake of (3)H-thymidine to measure blastogenesis. With pokeweed mitogen as the stimulus, transformation of normal lymphocytes in sera of alcoholics with either normal or fatty livers was not significantly different from that obtained in pooled human serum (PHS). However, in sera of patients with either alcoholic hepatitis or inactive cirrhosis mean transformation was significantly reduced (P <0.001, <0.02 respectively). With phytohaemagglutinin-P or concanavalin A as mitogens, suppression of transformation was not as marked but followed the same pattern. A significant negative correlation was observed between the magnitude of transformation and serum bilirubin and aspartate aminotransferase levels. An intra-patient comparison of the effects on transformation of normal lymphocytes by simultaneously collected peripheral and portal venous sera, and of peripheral sera obtained before and after portasystemic shunt surgery, indicated that the factor(s) responsible did not originate in the splanchnic circulation nor did it accumulate in the serum because of failed hepatic clearance. By performing transformation experiments in the presence of inhibitory patient sera diluted with PHS it was possible to show that these sera caused true inhibition of transformation rather than suppression due to failure to sustain cell culture because of nutritional deficiencies. Inhibitory sera did not contain high levels of the enzyme thymidine phosphorylase and did not significantly inhibit binding of (125)I-labelled mitogens to the lymphocyte surface. These findings indicate that the inhibitory effect of sera from alcoholics is of potential in vivo importance, that the effect increases with the degree of heptocyte damage, and that it is unrelated to the nonhepatic metabolic affects of chronic alcoholism.

摘要

采用丝裂原诱导的(3)H-胸腺嘧啶核苷摄取来测量细胞增殖,研究了酒精性肝病患者血清对体外淋巴细胞转化的影响。以商陆丝裂原为刺激物,正常肝脏或脂肪肝的酒精性肝病患者血清中正常淋巴细胞的转化与正常人混合血清(PHS)中淋巴细胞的转化无显著差异。然而,酒精性肝炎或静止期肝硬化患者血清中的平均转化显著降低(分别为P<0.001,<0.02)。以植物血凝素-P或刀豆球蛋白A作为丝裂原,转化的抑制作用不那么明显,但遵循相同的模式。观察到转化程度与血清胆红素和天冬氨酸转氨酶水平之间存在显著的负相关。对同时采集的外周血和门静脉血清对正常淋巴细胞转化的影响,以及门体分流术前和术后获得的外周血血清进行患者体内比较,结果表明,相关因素并非源于内脏循环,也不是由于肝脏清除功能衰竭而在血清中蓄积。通过在存在用PHS稀释的抑制性患者血清的情况下进行转化实验,有可能表明这些血清导致了真正的转化抑制,而不是由于营养缺乏导致细胞培养无法维持而产生的抑制作用。抑制性血清中不含有高水平的胸苷磷酸化酶,也不会显著抑制(125)I标记的丝裂原与淋巴细胞表面的结合。这些发现表明,酒精性肝病患者血清的抑制作用在体内具有潜在重要性,该作用随着肝细胞损伤程度的增加而增强,并且与慢性酒精中毒的非肝脏代谢影响无关。

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