Jansen J L, Koene R A, Kamp G J, Hagemann J F, Wijdeveld P G
J Immunol. 1975 Aug;115(2):392-4.
Pure 7S IgG2 was prepared from B6AF1 anti-B10.D2 ascites fluid by affinity chromatography. This preparation was extensively absorbed with B10.D2 red blood cells to remove the antibodies directed against the serologically defined antigens of the major histocompatibility complex. After absorption the serum had retained in vitro cytotoxic activity against 45 percent of B10.D2 spleen cells. The absorbed and unabsorbed 7S IgG2 antibodies were tested for their capacity to induce enhancement and, in the presence of rabbit complement, hyperacute rejection of B10.D2 skin grafts in B6AF1 recipient mice. The enhancing capacity of 7S IgG2 was completely unimpaired after absorption. However, the absorbed preparation was unable to induce hyperacute rejection of the grafts even if very high doses were administered. The results show that hyperacute rejection of skin grafts in this model is mediated by antibodies directed against the serologically defined antigens (i.e., H-2K antigens) of the H-2 complex. They further support the hypothesis that immunologic enhancement is mediated by antibodies directed against Ir-region-as-sociated antigens.
通过亲和层析从B6AF1抗B10.D2腹水制备纯7S IgG2。该制剂用B10.D2红细胞进行广泛吸收,以去除针对主要组织相容性复合体血清学定义抗原的抗体。吸收后,血清对45%的B10.D2脾细胞仍保留体外细胞毒性活性。测试吸收和未吸收的7S IgG2抗体诱导增强的能力,以及在兔补体存在下对B6AF1受体小鼠B10.D2皮肤移植的超急性排斥反应。吸收后7S IgG2的增强能力完全未受损。然而,即使给予非常高的剂量,吸收后的制剂也无法诱导移植皮片的超急性排斥反应。结果表明,该模型中皮肤移植的超急性排斥反应由针对H-2复合体血清学定义抗原(即H-2K抗原)的抗体介导。它们进一步支持了免疫增强由针对Ir区相关抗原的抗体介导的假说。