Kulikovskaia N V, Kapina M A, Kalinina O A, Chernousova L N
Probl Tuberk. 1996(1):43-6.
Immunization of BALB/c mice with sonicates of M. smegmatis and kansasii and fusion of splenocytes of the immunized mice with cells of syngeneic myeloma P3X63Ag8653 yielded hybrid clones synthetizing antibodies to these antigens. The selection of hybrid clones and analysis of the antibodies specificity were performed at ELISA using the immunization antigens and antigens from other mycobacteria and E. coli. To define immunoglobulin class of the antibodies the authors used antiglobulin sera of class A, M, G. The monoclonal antibodies belonged to IgG. Molecular mass of polypeptides carrying the epitope against which the antibodies were directed was measured at immunoblotting. Two antibodies reacted only with M. smegmatis, 38 and 10 kD proteins. The other 2 cross-reacted with other mycobacteria and were directed against epitopes on polypeptides varying in molecular mass.
用耻垢分枝杆菌和堪萨斯分枝杆菌的超声裂解物免疫BALB/c小鼠,并将免疫小鼠的脾细胞与同基因骨髓瘤P3X63Ag8653细胞融合,获得了合成针对这些抗原的抗体的杂交克隆。使用免疫抗原以及来自其他分枝杆菌和大肠杆菌的抗原,通过ELISA进行杂交克隆的筛选和抗体特异性分析。为确定抗体的免疫球蛋白类别,作者使用了A、M、G类抗球蛋白血清。单克隆抗体属于IgG。通过免疫印迹法测定了携带抗体所针对表位的多肽的分子量。两种抗体仅与耻垢分枝杆菌的38 kD和10 kD蛋白发生反应。另外两种抗体与其他分枝杆菌发生交叉反应,且针对分子量不同的多肽上的表位。