Neefe J R, Sachs D H
J Exp Med. 1976 Oct 1;144(4):996-1008. doi: 10.1084/jem.144.4.996.
Monolayers formed of normal mouse spleen cells attached to polystyrene coated with poly-L-lysine were tested for their ability to bind specifically antigen-reactive cells in normal or primed mouse spleen. 88 to greater than 98% of the activity of cytotoxic populations was removed by a single adsorption. However, normal spleen cells or spleen cells previously primed in vitro could not be depleted of their capacity to be sensitized, even when adsorption effectively removed all residual cytotoxic activity from the same previously primed population. In fact, exposure to an immunoadsorbent augmented the ultimate cytotoxicity generated in a nonspecific fashion. This augmentation was especially dramatic in the case of a previously primed population and may have reflected the removal of a nonspecific suppressor. If antigen-reactive precursors cannot be removed efficiently by adsorption, other approaches to the generation of tolerant lymphoid populations, such as specific suppression of precursor differentiation must be sought.
对由附着在涂有聚-L-赖氨酸的聚苯乙烯上的正常小鼠脾细胞形成的单层细胞,检测其结合正常或经致敏的小鼠脾中特异性抗原反应性细胞的能力。单次吸附可去除88%至超过98%的细胞毒性群体活性。然而,正常脾细胞或先前在体外致敏的脾细胞,即使吸附有效去除了同一先前致敏群体中所有残留的细胞毒性活性,其致敏能力也不会被耗尽。事实上,暴露于免疫吸附剂会以非特异性方式增强最终产生的细胞毒性。这种增强在先前致敏群体的情况下尤为显著,可能反映了非特异性抑制因子的去除。如果抗原反应性前体细胞不能通过吸附有效去除,就必须寻求其他产生耐受淋巴细胞群体的方法,例如特异性抑制前体细胞分化。