David J R, Schlossman S F
J Exp Med. 1968 Dec 1;128(6):1451-9. doi: 10.1084/jem.128.6.1451.
The immunochemical specificity of antigen-induced inhibition of peritoneal exudate cell migration was studied in animals sensitized to chemically defined alpha,DNP(Lys)(18) peptides. It was shown that sensitized peritoneal exudate cells could discriminate between various DNP-oligolysines. Only immunogenic members of the homologous series of alpha,DNP-L-lysines equal to or larger in size than the heptamer inhibited the migration of specifically sensitized peritoneal exudate cells. In contrast, nonimmunogenic alpha,DNP-L-lysines, a D-lysine containing stereoisomer of alpha,DNP L(Lys)(9) (alpha,DNP-L(4)DL(4)) and (Lys)(9)epsilon, DNP were not inhibitory to the migration of peritoneal exudate cells derived from animals immunized to alpha,DNP(Lys)(18). The exquisite specificity of the in vitro reaction of sensitized cells with antigen contrasts with the previously observed in vivo or in vitro specificity of anti-alpha,-DNP(Lys)(n) antibody, but parallels the specificity of the in vivo delayed or anamnestic response. These results suggest the presence of a still undefined but highly specific binding site, which functions as the cellular receptor for antigen on the sensitized lymphoid cell or on some "processing" cell.
在对化学定义的α,DNP(赖氨酸)(18)肽致敏的动物中,研究了抗原诱导的腹膜渗出细胞迁移抑制的免疫化学特异性。结果表明,致敏的腹膜渗出细胞能够区分各种DNP - 寡聚赖氨酸。只有与七聚体大小相等或更大的同源系列α,DNP - L - 赖氨酸中的免疫原性成员才能抑制特异性致敏的腹膜渗出细胞的迁移。相比之下,非免疫原性的α,DNP - L - 赖氨酸、含D - 赖氨酸的α,DNP L(赖氨酸)(9)(α,DNP - L(4)DL(4))的立体异构体以及(赖氨酸)(9)ε,DNP对来自免疫于α,DNP(赖氨酸)(18)的动物的腹膜渗出细胞的迁移没有抑制作用。致敏细胞与抗原的体外反应的高度特异性与先前观察到的抗α,-DNP(赖氨酸)(n)抗体的体内或体外特异性形成对比,但与体内延迟或回忆反应的特异性相似。这些结果表明存在一个尚未明确但高度特异性的结合位点,它作为致敏淋巴细胞或某些“加工”细胞上抗原的细胞受体发挥作用。