Ortiz-Ortiz L, Weigle W O, Parks D E
J Exp Med. 1982 Sep 1;156(3):898-911. doi: 10.1084/jem.156.3.898.
The induction of tolerance in an anti-idiotypic response was attempted by in vivo exposure to excess idiotype. Monoclonal immunoglobulin from the anti-p-azobenzenearsonate (ABA) hybridoma R16.7 was used as a representative of cross-reactive idiotype-positive (CRI+) antibodies because this hybridoma protein (HP) shares one or more closely related public idiotypic determinants with the serum CRI in A/J mice. Immunologic unresponsiveness was established by a single injection of the R16.7 idiotype and persisted for at least 6 wk. The level of circulating anti-idiotypic antibodies in tolerized A/J mice was significantly depressed after immunogenic challenge with eigher antigen, ABA-keyhole limpet hemocyanin (KLH), or the idiotype R16.7 HP. Experimental depletion of anti-idiotypic antibodies by tolerization allowed assessment of immunoregulation within this altered idiotype-anti-idiotype network. Deregulation of idiotype expression in tolerized mice challenged with ABA-KLH was manifest with up to 96% of the anti-ABA antibodies cross-reacting with the R16.7 idiotype. This selective enhancement of a major idiotype was accomplished without substantial alteration of the level of the overall anti-hapten response. Both the unresponsiveness established in anti-idiotypic antibody-producing cells and the enhanced synthesis in idiotype-producing cells were stable upon adoptive transfer into lethally irradiated, syngeneic recipients. Finally, previous immunization with the antigen ABA-KLH interfered with the induction of unresponsiveness to the idiotype. This interference is presumed to be mediated by prior activation of anti-idiotypic cells and/or antibody because injection of antigen with tolerogenic idiotype did not abrogate tolerance induction.
通过体内暴露于过量的独特型来尝试诱导抗独特型反应中的耐受性。来自抗对氨基苯砷酸(ABA)杂交瘤R16.7的单克隆免疫球蛋白被用作交叉反应性独特型阳性(CRI+)抗体的代表,因为这种杂交瘤蛋白(HP)与A/J小鼠血清中的CRI共享一个或多个密切相关的公共独特型决定簇。通过单次注射R16.7独特型建立免疫无反应性,并持续至少6周。在用抗原ABA-钥孔戚血蓝蛋白(KLH)或独特型R16.7 HP进行免疫原性攻击后,耐受的A/J小鼠中循环抗独特型抗体的水平显著降低。通过耐受诱导对抗独特型抗体进行实验性消耗,使得能够评估这种改变的独特型-抗独特型网络内的免疫调节。在用ABA-KLH攻击的耐受小鼠中,独特型表达失调表现为高达96%的抗ABA抗体与R16.7独特型发生交叉反应。在不显著改变总体抗半抗原反应水平的情况下实现了主要独特型的这种选择性增强。在抗独特型抗体产生细胞中建立的无反应性以及在独特型产生细胞中增强的合成在过继转移到致死照射的同基因受体后都是稳定的。最后,先前用抗原ABA-KLH进行的免疫干扰了对独特型无反应性的诱导。这种干扰被推测是由抗独特型细胞和/或抗体的先前激活介导的,因为注射具有耐受原性独特型的抗原并没有消除耐受性诱导。