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[γ球蛋白制剂对体外商陆有丝分裂原诱导的免疫球蛋白产生的影响]

[The effect of gammaglobulin preparations on in vitro immunoglobulin production induced by pokeweed mitogen].

作者信息

Hashimoto F

出版信息

Hokkaido Igaku Zasshi. 1984 Jan;59(1):64-71.

PMID:6201426
Abstract

It has been recognized in the experiments of animals, that high dose of administration of IgG suppresses the immunoglobulin production in vitro, because of masking of antigen determinants. The study evaluated the effect of several gammaglobulin preparations on in vitro immunoglobulin production induced by pokeweed mitogen. And the effect of these preparations was estimated by following system. Mononuclear cells (5 X 10(5)/ml) were incubated (37 degrees C, 5% CO2) in the presence of gammaglobulin preparations (0.01 mg/ml-1.0 mg/ml). On the sixth day of culture, the cells were spun down, washed three times, resuspended in MEM without L-4,5 [3H]-leucine. After 24 hours, supernatants were harvested, and the concentration of immunoglobulin produced by mononuclear cells was analyzed by solid-phase RIA. And the results which have been obtained as follows. PWM induced immunoglobulin production (IgG) was analyzed in the presence of immunoglobulin preparations. Among these preparations, the suppressive effect of ISG was most significant, and the effect was dose dependent. S-sulfonated and PEG-treated preparations also suppressed the IgG production, but not so strong as ISG. In the suppressive effect between S-sulfonation and PEG treatment, no significant difference was found. Pepsin treated preparation had no suppressive effect. Not only IgG production, but also IgA, IgM production were suppressed by the co-culture of ISG, S-sulfonated, and PEG treated IgG. ISG inhibits directly the differentiation of B cells, and also induces the activation of suppressor T cells. ISG was considered to suppress immunoglobulin production in vitro by these both pathways. The suppressor T cells, which are induced by ISG, are radiation resistant, hydrocortisone resistant and same population with OKT 8 positive cells.

摘要

在动物实验中已经认识到,高剂量给予免疫球蛋白G(IgG)会抑制体外免疫球蛋白的产生,原因是抗原决定簇被掩盖。该研究评估了几种丙种球蛋白制剂对体外由商陆有丝分裂原诱导的免疫球蛋白产生的影响。并且通过以下系统评估这些制剂的效果。单核细胞(5×10⁵/ml)在丙种球蛋白制剂(0.01mg/ml - 1.0mg/ml)存在的情况下进行孵育(37℃,5%二氧化碳)。在培养的第六天,将细胞离心,洗涤三次,重悬于不含L - 4,5 [³H] - 亮氨酸的MEM中。24小时后,收集上清液,通过固相放射免疫分析(RIA)分析单核细胞产生的免疫球蛋白浓度。得到的结果如下。在免疫球蛋白制剂存在的情况下分析了商陆有丝分裂原诱导的免疫球蛋白产生(IgG)。在这些制剂中,免疫血清球蛋白(ISG)的抑制作用最为显著,且该作用呈剂量依赖性。经S - 磺化和聚乙二醇(PEG)处理的制剂也抑制IgG的产生,但不如ISG强烈。在S - 磺化和PEG处理之间的抑制作用方面,未发现显著差异。经胃蛋白酶处理的制剂没有抑制作用。不仅IgG的产生,而且IgA、IgM的产生也被ISG、经S - 磺化和PEG处理的IgG共培养所抑制。ISG直接抑制B细胞的分化,并且还诱导抑制性T细胞的活化。ISG被认为通过这两种途径抑制体外免疫球蛋白的产生。由ISG诱导的抑制性T细胞具有抗辐射、抗氢化可的松的特性,并且与OKT 8阳性细胞属于同一群体。

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