Wakefield J D, Thorbecke G J
J Exp Med. 1968 Jul 1;128(1):171-87. doi: 10.1084/jem.128.1.171.
White-pulp cells and whole spleen from donor mice immunized with sheep erythrocytes were transferred intravenously to heavily irradiated mice. The numbers of plaque-forming cells and the amount of hemagglutinating antibody produced after reexposure to antigen were measured. When reexposure to sheep erythrocytes was delayed, a much greater response occurred in the transferred cells. Peak responsiveness was reached at 24 hr after transfer. This "lag effect" was greatly reduced by repeated injections of 5-bromodeoxyuridine into the recipient mice prior to challenge with antigen. It was therefore concluded that much of the increase in responsiveness was due to a proliferation of "primed" cells after cell transfer. The fact that a significant response was given by the transferred cells in spite of 5-bromodeoxyuridine treatment suggested that some of the primed cells were nondividing. White pulp was a much richer source of responsive cells than was whole spleen.
用绵羊红细胞免疫的供体小鼠的白髓细胞和全脾,经静脉注射到受大剂量照射的小鼠体内。再次接触抗原后,测定形成空斑细胞的数量和产生的血凝抗体量。当再次接触绵羊红细胞的时间延迟时,转移细胞产生的反应要大得多。转移后24小时达到反应高峰。在用抗原攻击之前,给受体小鼠反复注射5-溴脱氧尿苷,这种“滞后效应”大大降低。因此得出结论,反应性增加的很大一部分是由于细胞转移后“致敏”细胞的增殖。尽管用了5-溴脱氧尿苷处理,转移细胞仍产生显著反应,这一事实表明一些致敏细胞不进行分裂。白髓比全脾含有更丰富的反应性细胞来源。