Luben R A, Mohler M A, Nedwin G E
J Clin Invest. 1979 Jul;64(1):337-41. doi: 10.1172/JCI109459.
The human lympholine osteoclast activating factor (OAF) is thought to be involved in several bone-destroying diseases. The current studies were designed to produce monoclonal antibodies against OAF for use in the subsequent design of immunoassays for OAF in clinical samples. Spleen cells from mice immunized with purified human OAF were hybridized with mouse plasmacytoma cells in vitro to yield hybridomas. Several clones of these hybridomas secreted into the culture medium antibodies, which neutralized the biological activity of OAF at dilutions as high as 1:100,000 relative to the initial culture medium. These antibodies did not interfere with the activities of parathyroid hormone in the same systems. These results represent the first report of monoclonal antibodies against a human lympholine, and validate the concept that hybridoma production is a useful technique for developing antibodies against weak or scarce antigens.
人淋巴细胞破骨细胞激活因子(OAF)被认为与多种骨质破坏疾病有关。当前的研究旨在制备抗OAF的单克隆抗体,用于随后设计针对临床样本中OAF的免疫测定法。用纯化的人OAF免疫的小鼠脾细胞在体外与小鼠浆细胞瘤细胞杂交,以产生杂交瘤。这些杂交瘤的几个克隆将抗体分泌到培养基中,相对于初始培养基,这些抗体在高达1:100,000的稀释度下中和了OAF的生物活性。这些抗体在相同系统中不干扰甲状旁腺激素的活性。这些结果代表了针对人淋巴细胞因子的单克隆抗体的首次报道,并验证了杂交瘤生产是开发针对弱或稀缺抗原的抗体的有用技术这一概念。