Epstein S L, Masakowski V R, Sharrow S O, Bluestone J A, Ozato K, Sachs D H
J Immunol. 1982 Oct;129(4):1545-52.
The effects of in vivo treatment with xenogeneic anti-idiotypic antibodies were examined in an anti-Ia idiotypic system. Monoclonal antibody 14-4-4S, specific for Ia.7, has been shown to bear idiotopes that are expressed at readily detectable levels in conventional alloantibody responses. Sera from mice treated with purified anti-idiotypic antibodies (anti-Id) were found to contain inhibitory activity in an ELISA specific for the 14-4-4S Id, whereas sera from control mice treated with heterologous normal Ig did not. In addition, sera of anti-Id-treated C3H.SW mice contained specific anti-I-E activity, shown by binding to B10.A(2R) but not B10.A(4R) LPS blasts in flow microfluorometry. The anti-I-E induced by anti-Id included more IgG1 than IgG2. Even though a significant amount of anti-I-E activity was present in the serum, absorption analysis showed that most of the idiotope-positive antibody was not I-Ek-specific. Penetrance of induction of anti-I-E by anti-Id was 100% in the C3H.SW mice tested, and activity persisted in the serum for at least 8 to 9 mo in some cases. B10 mice produced only marginal anti-I-E activity after treatment, suggesting that induction is due to specific triggering rather than due entirely to a resemblance of anti-Id to the I-E antigen. The results thus indicate long-lasting alterations in an anti-Ia idiotypic system in the absence of exposure to conventional antigen, and represent specific manipulation of anti-Ia immunity.
在一个抗Ia独特型系统中检测了用异种抗独特型抗体进行体内治疗的效果。对Ia.7特异的单克隆抗体14-4-4S已被证明带有独特型表位,这些表位在传统的同种异体抗体反应中以易于检测的水平表达。在用纯化的抗独特型抗体(抗Id)治疗的小鼠血清中,发现在针对14-4-4S独特型的ELISA中含有抑制活性,而用异源正常Ig治疗的对照小鼠血清则没有。此外,抗Id治疗的C3H.SW小鼠血清含有特异性抗I-E活性,在流式微量荧光测定中表现为与B10.A(2R) LPS母细胞结合,但不与B10.A(4R) LPS母细胞结合。抗Id诱导产生的抗I-E中IgG1比IgG2更多。尽管血清中存在大量抗I-E活性,但吸收分析表明,大多数独特型阳性抗体并非I-Ek特异性。在测试的C3H.SW小鼠中,抗Id诱导抗I-E的发生率为100%,在某些情况下,活性在血清中持续至少8至9个月。B10小鼠在治疗后仅产生少量抗I-E活性,这表明诱导是由于特异性触发,而不是完全由于抗Id与I-E抗原的相似性。因此,结果表明在未接触传统抗原的情况下,抗Ia独特型系统发生了持久的改变,代表了对抗Ia免疫的特异性操纵。