Kjellén L
Immunology. 1965 Jun;8(6):557-65.
Rabbit hyperimmune γ-globulin was produced against type 5 adenovirus. This was digested with pepsin to produce bivalent fragments of antibody. These fragments retained the capacity to precipitate with antigen, but were defective in their power to neutralize virus infectivity. Their neutralizing capacity deviated from that of native antibody in the following ways: 1. The proportion of virus neutralized was smaller. 2. The progressive neutralization of virus ceased within 10–15 minutes of mixing virus and fragments of antibody. 3. The rate of neutralization of virus depended only on the concentration of fragments of antibody, and was independent of the relative proportions of virus and antibody fragments. 4. Over the ranges tested the antibody fragments inactivated an approximately constant proportion of virus irrespective of the amount of virus used in the primary mixture. There is a brief discussion of the significance of these results for an understanding of the mechanism by which complete antibody neutralizes virus infectivity.
兔抗5型腺病毒超免疫γ球蛋白被制备出来。用胃蛋白酶对其进行消化以产生抗体的二价片段。这些片段保留了与抗原沉淀的能力,但在中和病毒感染性方面存在缺陷。它们的中和能力与天然抗体的中和能力有以下不同:1. 被中和的病毒比例较小。2. 病毒与抗体片段混合后10 - 15分钟内,病毒的逐步中和就停止了。3. 病毒的中和速率仅取决于抗体片段的浓度,与病毒和抗体片段的相对比例无关。4. 在测试范围内,无论初次混合物中使用的病毒量如何,抗体片段都能使大致恒定比例的病毒失活。文中简要讨论了这些结果对于理解完整抗体中和病毒感染性机制的意义。