绵羊免疫前后抗体的研究。

Annales immunologiae Hungaricae Pub Date : 1979-01-01
F Péterfy, M Lörinczi, K V Rajczy, E Monostori, L R Zsolnay, K Miklós, I Ormai, M Németh
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引用次数: 0

摘要

在很长一段时间内,从3只未免疫的羊连续抽取血清样本。从样品中分离出人血清白蛋白(HSA)、卵清蛋白(OA)和FITC抗体。然后,2只动物注射HSA+完全弗氏佐剂,3只动物注射无抗原佐剂。连续免疫后血清样品与免疫前血清样品采用相同的程序。特异性抗体浓度增加,只有刺激后抗体群能够沉淀。在抗原存在的情况下,刺激后抗体与淋巴细胞Fc受体的结合程度增加。无论是补体激活能力还是达到抗原抗体等效所需的抗原数量,免疫前后的抗体群体都没有差异。等电聚焦未发现与已有抗体不同的新条带。然而,在形成不同条带的抗体的相对参与中观察到变化。在免疫前和免疫后的抗体数量之间没有明显的限制。免疫后显示的Ig增加伴随着未给予抗原的动物的特异性抗体的类似增加,但在其他动物中没有。作者认为体液抗体已经在免疫反应的早期阶段发挥了作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies of pre- and postimmunization antibodies of sheep.

Serum samples were taken serially from three nonimmunized sheep over a long period of time. Antibodies to human serum albumin (HSA), ovalbumin (OA) and FITC were separated from the samples. Than, two of the animals were injected with HSA+ complete Freund's adjuvant, the third with adjuvant without antigen. Serial postimmunization serum samples were subjected to the same procedures as the pre-immunization ones. The specific antibodies increased in concentration, and only the postimmunization antibody population was able to precipitate. In the presence of the antigen, the postimmunization antibodies bound to the Fc receptors of lymphocytes to an increased degree. There was no difference between pre- and postimmunizaton antibody populations either in complement-activating capacity or in the quantity of antigen necessary for reaching antigen-antibody equivalence. Isoelectro-focusing showed no new bands which would indicate antibodies different from the pre-existing ones. However, changes were observed in the relative participation of the antibodies forming different bands. No sharp limit was observed between pre- and postimmunization antibody populations. The Ig increment demonstrated after immunization was accompanied by a similar increment in the specific antibodies tested in the animal that had not given antigen, but not in the others. The authors attribute a role to humoral antibodies already in the earliest phase of immune response.

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