Lin M, Zhou E M, Heckert R A
Virology Section, Animal Diseases Research Institute, Nepean, Ontario, Canada.
Viral Immunol. 1996;9(1):35-43. doi: 10.1089/vim.1996.9.35.
We previously generated rabbit polyclonal antiidiotypic antibody (anti-Id) to a murine monoclonal antibody (M1875) specific for the bluetongue virus core protein VP7, and demonstrated that this anti-Id (designated RAb2-A) had the characteristics of an internal image anti-Id (Ab2 beta). In this communication, RAb2-A was used to induce immune responses in sheep and the responses were compared to immunization with VP7. The immune sera were tested for the presence of anti-VP7 antibodies and the expression of the Id of M1875. Animals immunized with RAb2-A were able to produce M1875-like antibody responses, i.e., they recognized the same or a similar epitope as M1875 and possessed the M1875 Id, without subsequent exposure to the original antigen. This was demonstrated by showing that antibodies induced by RAb2-A (i) reacted specifically with the immunizing anti-Id, (ii) were capable of binding VP7, (iii) inhibited M1875 from binding to VP7, and (iv) inhibited M1875 from binding to RAb2-A. Animals immunized with purified VP7 produced antibodies that possessed the epitope and idiotope specificity of M1875. No antibody responses to VP7 were detected in control animals immunized with either rabbit anti-Id to the pseudorabies virus glycoprotein gII or BHK-21 cell proteins. We conclude that rabbit anti-Id RAb2-A serologically mimics an M1875-defined VP7 epitope sufficiently to function as a surrogate antigen for inducing anti-bluetongue virus VP7 responses.
我们之前制备了针对蓝舌病毒核心蛋白VP7的鼠单克隆抗体(M1875)的兔多克隆抗独特型抗体(抗Id),并证明该抗Id(命名为RAb2-A)具有内影像抗Id(Ab2β)的特征。在本通讯中,使用RAb2-A诱导绵羊的免疫反应,并将这些反应与用VP7免疫的反应进行比较。检测免疫血清中抗VP7抗体的存在以及M1875独特型的表达。用RAb2-A免疫的动物能够产生类似M1875的抗体反应,即它们识别与M1875相同或相似的表位,并具有M1875独特型,而无需随后接触原始抗原。这通过以下方式得到证明:由RAb2-A诱导的抗体(i)与免疫用抗Id特异性反应,(ii)能够结合VP7,(iii)抑制M1875与VP7结合,以及(iv)抑制M1875与RAb2-A结合。用纯化的VP7免疫的动物产生的抗体具有M1875的表位和独特型特异性。在用针对伪狂犬病病毒糖蛋白gII的兔抗Id或BHK-21细胞蛋白免疫的对照动物中未检测到对VP7的抗体反应。我们得出结论,兔抗Id RAb2-A在血清学上充分模拟了由M1875定义的VP7表位,足以作为诱导抗蓝舌病毒VP7反应的替代抗原。