Experimentelle Untersuchungen über Wirkungsweise und Dauer der Antikörper-bedingten Immunsuppression1

P. Emmerling , H. Finger, M. Müller
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Abstract

The simultaneous injection of either 108 or 5 × 105 sheep erythrocytes (SE) and an allogeneic anti-SE serum into mice produced not only a suppression of the primary immune response, but, moreover, the secondary immune reaction elicited, either 4, 8, 12, 16 or 30 weeks after the primary antigenic stimulation, was found to be impaired. This was mainly demonstrated by the significantly reduced numbers of 7S antibody-synthesizing spleen cells. The suppression of the secondary immune responses is hardly compatible with the conception that the antibody-mediated immunosuppression is solely due to an inactivation of the antigenic determinants by the passively administered specific antibody in the periphery of the immune system. This objection against the so-called «peripheric theory» is supported by a further finding. When mice primarily immunized by a simultaneous injection of 108 SE and anti-SE-serum were treated with 2 × 107 SE 24 hours before boostering with 108 SE, in order to eliminate a possibly existing residual activity of the passively administered specific antibodies given together with the primary antigenic stimulus, the secondary 7S response was likewise found to be significantly suppressed. On the basis of these findings it is suggested that besides the «peripheric mechanism» a «central» effect plays a significant role in the phenomenon of antibodymediated immunosuppression, this being due to the reversible or irreversible inactivation of immunocompetent precursor cells by the attachment of antigen-antibody-complexes which results in an inhibition of their differentiation into antibody-producing cells.

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关于药物作用的影响和持续时间的实验研究
在小鼠体内同时注射108或5 × 105羊红细胞(SE)和异基因抗SE血清,不仅可以抑制小鼠的初级免疫反应,而且在初级抗原刺激后4、8、12、16或30周引起的次级免疫反应也会受到损害。这主要表现为合成7S抗体的脾细胞数量明显减少。次级免疫反应的抑制很难与抗体介导的免疫抑制仅仅是由于抗原决定因子被被动给予免疫系统外周的特异性抗体灭活的概念相容。这一反对所谓“外围理论”的观点得到了进一步发现的支持。同时注射108 SE和抗SE血清免疫的小鼠,在108 SE增强前24小时用2 × 107 SE处理,以消除与初级抗原刺激一起被动给药的特异性抗体可能存在的残留活性,同样发现继发性7S反应被显著抑制。根据这些发现,除了“外周机制”外,“中枢”效应在抗体介导的免疫抑制现象中起着重要作用,这是由于抗原-抗体复合物的附着导致免疫活性前体细胞可逆或不可逆失活,从而抑制其分化为产生抗体的细胞。
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