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Studies on the induction and time course of repression of delayed hypersensitivity in the mouse by low and high doses of antigen

机译:低剂量和高剂量抗原诱导小鼠迟发型超敏反应的诱导和时间过程研究

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CAF1 and CF-1 female mice pretreated with small or large quantities of the protein antigens chicken egg albumin or human serum albumin had their capacities to develop delayed hypersensitivity and some humoral antibodies in response to injection of these antigens in Freund's incomplete adjuvant specifically repressed. Repression following a single intraperitoneal injection of 10 mg of human serum albumin in saline was maximal at 2 weeks. Two appropriately spaced pretreatments were approximately 100-fold more effectual than one in eliciting repression, perhaps because of a secondary antibody response. Pretreatment with antigen in an inefficient variety of Freund's incomplete adjuvant also induced immunologic repression both at high (100 and 10 mg) and very low (optimal = 0·01 γg) doses; but this repression was weaker than that following pretreatment with antigen in saline. One experiment comparing four injection routes for relative capacity to induce repression showed no one clearly superior to the others, although the intravenous route gave some indication of being so. Repression affecting induction of delayed hypersensitivity lasted for 12 weeks in CF-1 and 30 weeks in CAF1 mice, receded slowly thereafter, and was not followed by spontaneous sensitization. Among humoral antibody responses, pretreatment-induced repression affected Arthus sensitization, and passive haemagglutinin, precipitin and passive cutaneous anaphylaxis antibody production, roughly in descending order. Data from these experiments seem most compatible with the idea that the repression studied is active rather than passive and due, perhaps, to a humoral antibody which represses sensitization.
机译:用少量或大量蛋白质抗原鸡鸡蛋清蛋白或人血清白蛋白预处理的CAF1和CF-1雌性小鼠具有发展迟发型超敏反应的能力,并且响应于在弗氏不完全佐剂中注射这些抗原而产生了一些体液抗体,从而被特异性抑制。腹膜内注射10 mg人血清白蛋白的生理盐水后2周最大程度的抑制。可能是由于第二抗体反应,两种适当间隔的预处理在引发抑制方面的效果比一种有效约高100倍。在低剂量的弗氏不完全佐剂中用抗原进行预处理也可在高剂量(100和10 mg)和极低剂量(最佳= 0·01γg)时引起免疫抑制。但是这种抑制作用比用盐水中的抗原预处理后的抑制作用要弱。一项比较四种注射途径诱导抑制的相对能力的实验表明,没有一种方法明显优于其他方法,尽管静脉途径表明确实如此。抑制迟发型超敏反应诱导的抑制作用在CF-1中持续12周,在CAF1小鼠中持续30周,此后缓慢下降,并且没有随后的自发性致敏作用。在体液抗体反应中,预处理诱导的抑制作用会影响Arthus致敏性,并且被动血凝素,沉淀素和被动皮肤过敏反应抗体的产生大致按降序排列。来自这些实验的数据似乎与所研究的抑制是主动而不是被动的想法最相符,并且可能归因于抑制敏化的体液抗体。

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