Tsujisaki Masayuki, Masuya Jiro, Okada Yoshimasa, Jinnohara Tsuneharu, Sasaki Shigeru, Yachi Akira, Imai Kohzoh
Department of Internal Medicine (Section 1), Sapporo Medical University, School of Medicine, Sapporo, Japan.
J Clin Lab Anal. 2002;16(6):279-89. doi: 10.1002/jcla.10058.
In order to analyze the epitope structure of carcinoembryonic antigen (CEA) and the idiotype network system, seven anti-idiotypic monoclonal antibodies (anti-Id MoAbs) were generated from a BALB/c mouse immunized with anti-CEA MoAb P1-356, which recognized a synthetic peptide P1 of CEA, domain I. These MoAbs were divided into four groups. The anti-Id MoAbs specifically reacted with MoAb P1-356, but not with any MoAb, and inhibited the binding of MoAb P1-356 to CEA, indicating that all of these anti-Id MoAbs recognized private idiotopes at the combining sites of MoAb P1-356. Polyclonal anti-anti-idiotypic antiserum (Ab3) generated with anti-Id MoAbs M315 (Ab2), blocked the binding of MoAb P1-356 (Ab1) to CEA and reacted with CEA(Ag) and synthetic peptide P1. The analysis of serological assays suggested that it contains "Ab1-like Ab3." Therefore, we prepared anti-anti-Id MoAbs using anti-Id MoAb M315. Among 13 candidates, anti-anti-Id MoAb 11B2 was selected, because it competed with MoAb P1-356 (Ab1) binding to CEA. A direct binding assay using MoAb11B2 showed that it reacted with purified CEA and with CEA synthetic peptide P1. In addition, MoAb 11B2 (Ab3) reacted with both CEA-producing cultured cells and colonic cancerous tissues in immunostaining. These results indicate that anti-anti-Id MoAb 11B2 is "Ab1-like Ab3." Therefore, it is suggested that anti-Id MoAb M315 bears an "internal image" of the MoAb P1-356-defined epitope on CEA.
为了分析癌胚抗原(CEA)的表位结构和独特型网络系统,用识别CEA结构域I的合成肽P1的抗CEA单克隆抗体P1-356免疫BALB/c小鼠,产生了7种抗独特型单克隆抗体(抗Id单克隆抗体)。这些单克隆抗体分为4组。抗Id单克隆抗体与单克隆抗体P1-356特异性反应,但不与任何其他单克隆抗体反应,并抑制单克隆抗体P1-356与CEA的结合,表明所有这些抗Id单克隆抗体在单克隆抗体P1-356的结合位点识别其独特型表位。用抗Id单克隆抗体M315(Ab2)产生的多克隆抗抗独特型抗血清(Ab3),阻断了单克隆抗体P1-356(Ab1)与CEA的结合,并与CEA(Ag)和合成肽P1反应。血清学分析表明其含有“Ab1样Ab3”。因此,我们用抗Id单克隆抗体M315制备了抗抗Id单克隆抗体。在13个候选抗体中,选择了抗抗Id单克隆抗体11B2,因为它能与单克隆抗体P1-356(Ab1)竞争结合CEA。使用单克隆抗体11B2的直接结合试验表明,它能与纯化的CEA和CEA合成肽P1反应。此外,单克隆抗体11B2(Ab3)在免疫染色中与产生CEA的培养细胞和结肠癌组织均有反应。这些结果表明抗抗Id单克隆抗体11B2是“Ab1样Ab3”。因此,提示抗Id单克隆抗体M315具有CEA上由单克隆抗体P1-356定义的表位的“内影像”。