Zhou E M, Huang W
Virology Section, Animal Diseases Research Institute, Nepean, Ontario, Canada.
J Clin Microbiol. 1995 Apr;33(4):850-4. doi: 10.1128/jcm.33.4.850-854.1995.
Polyclonal anti-idiotypic antibodies (anti-Ids) were generated by the sequential immunization of rabbits with three mouse monoclonal antibodies (MAb1s) specific for a major bluetongue virus (BTV) protein, VP7. The anti-Ids, designated RAb2s, recognized idiotopes which were located within or near the antigen-combining sites of the MAb1s and were associated with both heavy and light chains of MAb1s. RAb2s inhibited the MAb1s from binding to BTV antigens, and their interaction with MAb1s was inhibited by BTV antigens. By recognizing the common idiotopes, RAb2s detected anti-BTV antibodies from bovine antisera; their interaction was also partially inhibited by BTV antigens. These results indicated that RAb2s recognized the common idiotopes on anti-VP7 antibodies obtained from mice and cattle and that at least a portion of RAb2s were internal-image anti-Ids that functionally mimicked VP7. RAb2s may be used to substitute for the tissue culture-derived viral antigen in currently used serological assays for the detection of antibodies to BTV.
通过用三种针对主要蓝舌病毒(BTV)蛋白VP7的小鼠单克隆抗体(MAb1)对兔子进行连续免疫,产生了多克隆抗独特型抗体(抗Id)。这些抗Id被命名为RAb2,它们识别位于MAb1抗原结合位点内或附近的独特型表位,并且与MAb1的重链和轻链都相关。RAb2抑制MAb1与BTV抗原的结合,并且它们与MAb1的相互作用被BTV抗原抑制。通过识别共同的独特型表位,RAb2检测牛抗血清中的抗BTV抗体;它们的相互作用也被BTV抗原部分抑制。这些结果表明,RAb2识别从小鼠和牛获得的抗VP7抗体上的共同独特型表位,并且至少一部分RAb2是在功能上模拟VP7的内影像抗Id。RAb2可用于替代目前用于检测BTV抗体的血清学检测中组织培养衍生的病毒抗原。