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系统性红斑狼疮中的白细胞迁移抑制试验(LMIT)

Leukocyte migration inhibition test (LMIT) in systemic lupus erythematosus.

作者信息

Tanaka K, Yamauchi Y, Horimatsu T, Isobe T, Imura H

出版信息

Microbiol Immunol. 1978;22(12):785-92. doi: 10.1111/j.1348-0421.1978.tb00432.x.

Abstract

A leukocyte migration inhibition test (LMIT) utilizing the agarose gel technique was performed with native DNA as an antigen in ten patients with systemic lupus erythematosus (SLE) and five normal subjects. Irrespective of disease activity, supernatants obtained at different time intervals during lymphocyte culture in eight patients with SLE showed significant alteration of migration, either enhancement or inhibition, of normal leukocytes. However, supernatants in the control experiments produced no significant alteration of migration. Polyacrylamide gel electrophoresis of supernatants obtained from the SLE group revealed that the inhibitory activity was present in the albumin region, whereas the enhancement activity was found in the beta-globulin region. These results indicate that the hitherto employed estimation of the leukocyte migration inhibition test based on the total activity of these two factors is insufficient for accurate evaluation of chemical mediators from sensitized lymphocytes and that the separation of these two factors may be important for a greater understanding of cellular immunity.

摘要

以天然DNA为抗原,利用琼脂糖凝胶技术对10例系统性红斑狼疮(SLE)患者和5名正常受试者进行了白细胞迁移抑制试验(LMIT)。无论疾病活动情况如何,8例SLE患者淋巴细胞培养过程中在不同时间间隔获得的上清液均显示正常白细胞迁移发生了显著改变,表现为增强或抑制。然而,对照实验中的上清液未产生显著的迁移改变。对SLE组获得的上清液进行聚丙烯酰胺凝胶电泳显示,抑制活性存在于白蛋白区域,而增强活性则在β-球蛋白区域被发现。这些结果表明,迄今为止基于这两种因子的总活性进行的白细胞迁移抑制试验评估,不足以准确评估致敏淋巴细胞产生的化学介质,并且分离这两种因子对于更深入理解细胞免疫可能很重要。

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