Haynes J D, Rosenstein R W, Askenase P W
J Immunol. 1978 Mar;120(3):886-94.
Hapten-specific delayed time course skin reactions containing predominant accumulations of basophils and eosinophils were elicited in newborn guinea pigs after i.v. transfer of small amounts of oxazolone immune serum. The immune serum was fractionated by column chromatography procedures, and the fractions were examined for their ability in transferring this form of cutaneous basophil hypersensitivity (CBH). Only the 7S IgG-containing peak from Sephadex G-200 columns, and only the IgG1-containing fractions from DEAE columns, transferred CBH. An affinity column of bound oxazolone removed the activity from immune serum, and it could be recovered from the column by eluting with soluble oxazolone. About 35 microgram of purified IgG1 anti-oxazolone antibody could systemically transfer CBH reactivity. An immunoadsorbant column of anti-IgG1 removed this activity, but a column of anti-IgG2 did not. None of the procedures were able to separate activity in transferring CBH from passive cutaneous anaphylactic (PCA) activity classically associated with guinea pig IgG1 antibody. IgG1 from 8-day immune and 31-day hyperimmune donors were both effective. The average association constant of 8-day antibody was 8 X 10(-4) M-1. Transfer of cutaneous basophil reactions can be mediated by low affinity serum 7S IgG1 antibody.
静脉注射少量恶唑酮免疫血清后,新生豚鼠会引发含有大量嗜碱性粒细胞和嗜酸性粒细胞的半抗原特异性延迟时程皮肤反应。通过柱色谱法对免疫血清进行分离,并检测各组分传递这种皮肤嗜碱性粒细胞超敏反应(CBH)的能力。只有来自Sephadex G - 200柱的含7S IgG的峰,以及来自DEAE柱的含IgG1的组分能够传递CBH。结合恶唑酮的亲和柱可去除免疫血清中的活性,通过用可溶性恶唑酮洗脱可从柱上回收活性。约35微克纯化的IgG1抗恶唑酮抗体可全身传递CBH反应性。抗IgG1免疫吸附柱可去除这种活性,但抗IgG2柱则不能。所有这些方法均无法将传递CBH的活性与经典上与豚鼠IgG1抗体相关的被动皮肤过敏反应(PCA)活性分开。来自8天免疫和31天超免疫供体的IgG1均有效。8天抗体的平均结合常数为8×10⁻⁴M⁻¹。皮肤嗜碱性粒细胞反应的传递可由低亲和力血清7S IgG1抗体介导。