Mistretta V I, Cavalier E, Collette J, Chapelle J P
Service de Chimie Médicale, CHU de Liège, Belgique.
Rev Med Liege. 2009 May-Jun;64(5-6):248-52.
In contrast to a polyclonal antiserum, a monoclonal antibody is specific to a single epitope on the surface of a complex antigen. In 1975, Kohler and Milstein produced the first monoclonal antibodies by using a method which rapidly became a key technology in immunology. By fusing activated antibody-forming cells (B cells) with myeloma cells, they obtained hybrid cells--the so-called hydridomas--which combine the ability of the activated B cells to secrete a single species of antibody and the immortality of the myeloma cell. The selected hybridomas proliferate continuously, their clonal progeny providing an unending supply of antibody with a single specificity. These antibodies have found many applications in basic research and in vitro diagnosis. In the clinical laboratory, monoclonal antibodies are used as reagents in immunoassays, often replacing traditional antisera. Many years of development and innovation were needed to humanize monoclonal antibodies in order to make them usable in human therapy.
与多克隆抗血清不同,单克隆抗体对复杂抗原表面的单个表位具有特异性。1975年,科勒和米尔斯坦通过一种迅速成为免疫学关键技术的方法制备了首批单克隆抗体。他们将活化的抗体形成细胞(B细胞)与骨髓瘤细胞融合,获得了杂交细胞——即所谓的杂交瘤——它兼具活化B细胞分泌单一抗体的能力和骨髓瘤细胞的永生性。筛选出的杂交瘤持续增殖,其克隆后代源源不断地提供具有单一特异性的抗体。这些抗体在基础研究和体外诊断中得到了广泛应用。在临床实验室中,单克隆抗体用作免疫测定的试剂,常常取代传统抗血清。为了使单克隆抗体能够用于人类治疗,需要经过多年的研发与创新来实现其人源化。