Ptak W, Gumińska M, Stachurska B, Czarnik Z
Int Arch Allergy Appl Immunol. 1977;53(2):145-51. doi: 10.1159/000231745.
alpha-Globulins prepared from different biological sources (human and bovine sera, mouse ascitic fluid, human ovarian cyst fluid) were separated by ion exchange chromatography on DEAE-cellulose into fractions A, B and C. Whereas fractions A and B had no immunosuppressive activity, fraction C injected into mice shortly before antigen administration, but not after, significantly inhibited the contact sensitivity to oxazolone. Single high doses were preferential over divided doses given on several occasions. In transfer experiments when cells of animals sensitized to oxazolone were injected into recipients treated previously with fraction C, the response was also inhibited. Fraction C, when administered into F1 hybrid mice before injection of parental splenocytes, prevented the development of GVH reaction. The authors point out that the critical concentration of alpha-globulins at the time of antigen administration is necessary to make T-lymphocytes hyporesponsive, and when once triggered by antigen they become refractory to alpha-globulins action.
从不同生物来源(人血清和牛血清、小鼠腹水、人卵巢囊肿液)制备的α球蛋白,通过在DEAE - 纤维素上进行离子交换色谱法分离为A、B和C组分。A和B组分没有免疫抑制活性,而在抗原给药前不久(而非之后)注射到小鼠体内的C组分,显著抑制了对恶唑酮的接触敏感性。单次高剂量优于多次给予的分剂量。在转移实验中,当将对恶唑酮致敏的动物细胞注射到先前用C组分处理过的受体中时,反应也受到抑制。在向F1杂种小鼠注射亲本脾细胞之前给予C组分,可防止移植物抗宿主反应的发生。作者指出,在抗原给药时α球蛋白的临界浓度对于使T淋巴细胞反应低下是必要的,并且一旦被抗原触发,它们就会对抗α球蛋白的作用。