Moreno C, Hale C, Hewett R
Clin Exp Immunol. 1978 Mar;31(3):499-511.
Benzyl penicillin was coupled directly to the hydroxylic groups of dextrans and levans, and indirectly to the amino groups of diaminopropyl-carboxymethyl-levans. Derivatives of both types were tested for their capacity to react with anti-penicilloyl antibodies, either (immunoprecipitation and its inhibition) or (inhibition of PCA reaction). Only derivatives coupled to diaminopropyl-carboxymethyl-levans were active by both criteria. High molecular weight penicilloyl-diaminopropyl-carboxymethyl-levans were tested for their immunogenicity (IgM response) and capacity to induce tolerance in the IgE component of anti-penicilloyl responses in DBA/2 and CBAT6T6 mice. The IgM response to the levan carrier was very much depressed by penicilloyl substitution of the levan, whilst that to the penicilloyl determinants was also very poor. These derivatives induced a state of IgE antibody tolerance when given before or after the induction of an allergic response with penicilloyl-ovalbumin. A higher degree of substitution was required for the induction of tolerance after immunization. The tolerance induced was specific, since it did not affect IgE responses against ovalbumin and persisted for at least 3 months. Further challenges with penicilloyl-ovalbumin did not break the tolerant status.
苄青霉素直接与葡聚糖和左聚糖的羟基结合,间接与二氨基丙基 - 羧甲基 - 左聚糖的氨基结合。对这两种类型的衍生物进行了测试,以检测它们与抗青霉噻唑抗体发生反应的能力,反应方式包括(免疫沉淀及其抑制)或(PCA反应的抑制)。只有与二氨基丙基 - 羧甲基 - 左聚糖偶联的衍生物在这两种标准下都具有活性。对高分子量的青霉噻唑 - 二氨基丙基 - 羧甲基 - 左聚糖进行了免疫原性(IgM反应)测试,以及在DBA/2和CBAT6T6小鼠中诱导抗青霉噻唑反应的IgE成分产生耐受性的能力测试。左聚糖的青霉噻唑取代使对左聚糖载体的IgM反应大大降低,而对青霉噻唑决定簇的反应也很差。在用青霉噻唑 - 卵清蛋白诱导过敏反应之前或之后给予这些衍生物,会诱导IgE抗体耐受状态。免疫后诱导耐受需要更高程度的取代。诱导的耐受是特异性的,因为它不影响针对卵清蛋白的IgE反应,并且至少持续3个月。用青霉噻唑 - 卵清蛋白进一步激发不会打破耐受状态。