Kelsoe G
Cell Immunol. 1986 Mar;98(1):145-55. doi: 10.1016/0008-8749(86)90275-3.
Idiotope-specific immunoenhancement or suppression was induced in C57BL/6 mice by the injection of physiological amounts (100 ng-10 micrograms) of monoclonal anti-idiotope antibody. As previously described, nanogram doses enhanced idiotope expression while a 10-micrograms dose of anti-idiotope antibody induced the activation of a population of Thy 1.2+, Lyt 1-, 2+ suppressors. Both positive and negative regulatory activities were confined to the non-mu, idiotope+ compartment of the plaque-forming cell response. Administration of intermediate doses of anti-idiotope antibody resulted in an immune state indistinguishable from that of naive mice. This apparently normal response was in fact the product of a simultaneous activation of balanced enhancing and suppressive activities. When treated with anti-Lyt 2 or Lyt 1 and complement, spleen cell populations taken from such phenotypically "naive" mice revealed latent idiotope-specific immunoenhancement or suppression, demonstrating the components of a functional regulatory equilibrium.
通过注射生理剂量(100纳克 - 10微克)的单克隆抗独特型抗体,在C57BL / 6小鼠中诱导了独特型特异性免疫增强或抑制。如前所述,纳克剂量增强了独特型表达,而10微克剂量的抗独特型抗体诱导了一群Thy 1.2 +、Lyt 1 -、2 +抑制细胞的激活。正向和负向调节活性均局限于形成噬斑细胞反应的非μ、独特型+区室。给予中等剂量的抗独特型抗体导致一种与未免疫小鼠无法区分的免疫状态。这种明显正常的反应实际上是同时激活平衡的增强和抑制活性的产物。当用抗Lyt 2或Lyt 1及补体处理时,从此类表型“未免疫”小鼠获取的脾细胞群体显示出潜在的独特型特异性免疫增强或抑制,证明了功能调节平衡的组成部分。