Papoian R, Talal N
J Immunol. 1980 Feb;124(2):515-9.
The genetic contribution of the parental NZB and NZW mouse to the antigen-induced, macrophage-dependent, lymph node T cell proliferative response to d-DNA-mBSA was studied in F1 hybrid NZB/NZW (B/W) mice. Mice were immunized subcutaneously in the tail with denatured DNA-methylated BSA. Primed T cells from these mice were obtained after passage of immune periaortic and inguinal lymph node cells through nylon wool. The primed T cells were exposed in vitro to d-DNA-mBSA presented on spleen cells from BALB/c, DBA/2, NZB, NZW, or B/W mice. Immune B/W T cells gave a substantial proliferative response only in the presence of antigen-presenting cells from B/W or NZW mice. These results suggest that the response of B/W mice to DNA occurs primarily through the NZW H-2 haplotype of their own antigen-presenting cells.
在F1杂交NZB/NZW(B/W)小鼠中,研究了亲代NZB和NZW小鼠对变性DNA - 甲基化牛血清白蛋白(d-DNA-mBSA)的抗原诱导、巨噬细胞依赖性、淋巴结T细胞增殖反应的遗传贡献。用变性DNA - 甲基化牛血清白蛋白对小鼠尾部进行皮下免疫。在免疫的主动脉周围和腹股沟淋巴结细胞通过尼龙毛柱后,从这些小鼠中获得致敏T细胞。将致敏T细胞在体外暴露于来自BALB/c、DBA/2、NZB、NZW或B/W小鼠的脾细胞呈递的d-DNA-mBSA。免疫的B/W T细胞仅在存在来自B/W或NZW小鼠的抗原呈递细胞时才产生显著的增殖反应。这些结果表明,B/W小鼠对DNA的反应主要通过其自身抗原呈递细胞的NZW H-2单倍型发生。