Tite J P, Morrison C A, Taylor R B
Immunology. 1981 Feb;42(2):355-62.
The photosensitive affinity label NAP (4-azido-2-nitrophenyl) was used to make a stable covalent-bonded monomeric immune complex (Ag2Ab) between rabbit anti-NAP antibody and a bihaptenic compound containing NAP linked to fluorescein (NAP-aminocaproyl-lysyl-Fl). This complex injected into mice had marked effects on their subsequent response to fluorescein coupled to a thymus-independent carrier (Fl-ficoll). Depending on the time at which the complex was administered relative to challenge, it was possible to obtain either enhancing or suppressive effects. The enhancing but not the suppressive effect of complex was dependent on immune recognition of the rabbit IgG carrier. While the suppressive effect probably results from complex-mediated inactivation of T-independent B cells, it is suggested that the enhancing effect results from priming of the T-dependent B cells by Fl-Ficoll followed by their triggering into antibody production by rabbit IgG-specific helper cells.
使用光敏亲和标记物 NAP(4-叠氮基-2-硝基苯基)在兔抗 NAP 抗体与一种含有与荧光素相连的 NAP 的双半抗原化合物(NAP-氨基己酰-赖氨酰-Fl)之间形成稳定的共价结合单体免疫复合物(Ag2Ab)。将这种复合物注射到小鼠体内,对它们随后对与胸腺非依赖性载体偶联的荧光素(Fl-菲可)的反应产生显著影响。根据复合物给药时间相对于攻击时间的不同,有可能获得增强或抑制作用。复合物的增强作用而非抑制作用依赖于对兔 IgG 载体的免疫识别。虽然抑制作用可能是由复合物介导的胸腺非依赖性 B 细胞失活导致的,但有人认为增强作用是由 Fl-菲可引发依赖性 B 细胞,随后由兔 IgG 特异性辅助细胞触发其产生抗体所致。