Stimlation of Humoral Immunity by Peptidoglycan Monomer from Brevibacterium Divaricatum

I. Hršak , J. Tomašić, K. Pavelić, Z. Valinger
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引用次数: 10

Abstract

Peptidoglycan monomer (PGM), a water soluble and nontoxic disaccharide pentapeptide unit obtained from Brevibacterium divaricatum, was administered intravenously into mice, and the humoral immune response to sheep erythrocytes was assayed by means of Jerne's technique for plaque-forming cells (PFC) in the spleen. The PFC response was evidently stimulated. The counts were increased to practically the same extent over a great range of doses of PGM (from 25 to 1600 μg per animal), and the effect was present in the mice immunised with optimal, as well as in those immunised with suboptimal, doses of antigen. The magnitude of the immunostimulation depended only on the timing of PGM administration: it was maximal if PGM was injected 1 or 2 days after the antigen. In vitro, in a 4-day culture of spleen cells, PGM did not stimulate PFC formation. We conclude that stimulation of the humoral immune response to sheep red blood cell antigens by PGM probably occurs without cell multiplication and probably involves more than simply a contact of immunocompetent cells with PGM.

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短杆菌肽聚糖单体对体液免疫的刺激作用
肽聚糖单体(PGM)是一种从短杆菌中提取的水溶性、无毒的双糖五肽单位,我们将其静脉注射到小鼠体内,并用Jerne的脾脏斑块形成细胞(PFC)技术检测其对绵羊红细胞的体液免疫反应。PFC反应明显受到刺激。在大剂量的PGM剂量范围内(每只动物从25到1600 μg),计数几乎增加到相同的程度,并且在用最佳剂量的抗原免疫的小鼠和用次最佳剂量的抗原免疫的小鼠中都存在这种影响。免疫刺激的程度仅取决于PGM给药的时间:如果PGM在抗原后1或2天注射,则免疫刺激最大。在体外培养的4天脾细胞中,PGM不刺激PFC形成。我们得出的结论是,PGM对绵羊红细胞抗原的体液免疫反应的刺激可能不需要细胞增殖,可能不仅仅涉及免疫能力细胞与PGM的接触。
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