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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抑制作用。

The suppressive effect of gammaglobulin preparations on in vitro pokeweed mitogen-induced immunoglobulin production.

作者信息

Hashimoto F, Sakiyama Y, Matsumoto S

出版信息

Clin Exp Immunol. 1986 Aug;65(2):409-15.

Abstract

The effect of the supplementation with several gammaglobulin (GG) preparations on the in vitro immunoglobulin synthesis of peripheral blood mononuclear cells (PBMC) from normal subjects stimulated with pokeweed mitogen (PWM) was studied. Among the GG preparations used in this study, immune serum globulin (ISG) demonstrated the most suppressive effect, and S-sulfonation and polyethylene glycol (PEG)-treated preparations also had a suppressive effect. However, the preparation of pepsin degradation had no suppressive effect. And because IgG F(ab')2 fragments also failed to induce the suppressive effect, it was considered to be triggered by the attachment of the Fc portion of GG to the corresponding membrane receptor. To determine the cellular targets, PBMC were fractionated into E-rosetting cells (T cells) and non E-rosetting cells (B cells). The suppressive effect was induced by pre-incubation of either T cells or B cells with the GG preparations for 1 h, at 37 degrees C in PWM-induced immunoglobulin (Ig) production. The failure of T cells pretreated with OKT8 monoclonal antibody and complement to induce the suppressive effect suggested that T8 positive T cells are one of the effector cells involved. The activation step of the suppressive effect was prostaglandin E2-independent, and as effector cells contain an Fc receptor which is sensitive to pronase, it was suggested that monocytes were not involved in this activation process. Our observations further suggested that the Ig effects of GG therapy are not limited to antibody transfer, since GG preparations also suppress directly the differentiation of B cells and induce suppressor T cells in in vitro immunoglobulin production stimulated with PWM.

摘要

研究了几种丙种球蛋白(GG)制剂对正常受试者经商陆丝裂原(PWM)刺激的外周血单个核细胞(PBMC)体外免疫球蛋白合成的影响。在本研究中使用的GG制剂中,免疫血清球蛋白(ISG)表现出最强的抑制作用,经S-磺化和聚乙二醇(PEG)处理的制剂也有抑制作用。然而,胃蛋白酶降解制剂没有抑制作用。并且由于IgG F(ab')2片段也未能诱导抑制作用,因此认为是GG的Fc部分与相应膜受体结合引发了该抑制作用。为了确定细胞靶点,将PBMC分为E花环形成细胞(T细胞)和非E花环形成细胞(B细胞)。在PWM诱导的免疫球蛋白(Ig)产生过程中,将T细胞或B细胞与GG制剂在37℃预孵育1小时可诱导抑制作用。用OKT8单克隆抗体和补体预处理的T细胞未能诱导抑制作用,这表明T8阳性T细胞是参与的效应细胞之一。抑制作用的激活步骤不依赖前列腺素E2,并且由于效应细胞含有对链霉蛋白酶敏感的Fc受体,因此表明单核细胞不参与该激活过程。我们的观察结果进一步表明,GG治疗的Ig作用不仅限于抗体转移,因为GG制剂在PWM刺激的体外免疫球蛋白产生中也直接抑制B细胞的分化并诱导抑制性T细胞。

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