Tachibana H, Shirahata S, Kawahara H, Murakami H
Graduate School of Genetic Resources Technology, Faculty of Agriculture, Kyushu University, Fukuoka, Japan.
Cytotechnology. 1991 Sep;7(1):1-6. doi: 10.1007/BF00135632.
Two cell lines of human hybridomas were fused to generate hybrid antibodies. One human hybridoma cell line was HT2 producing IgM monoclonal antibody (MAb) reactive to carboxy peptidase A (Cpase) and double stranded DNA (ds DNA) and another was SU-1-D2 secreting IgM MAb reactive to ds DNA but not to Cpase. Most hybrid hybridomas obtained by fusion of the two hybridomas secreted hybrid antibodies exhibiting increased antigen binding strengths. All of the hybrid antibodies with increased binding strengths against Cpase and ds DNA contained only the light chains derived from SU-1-D2. These results suggested that increase in the binding strength of the hybrid antibodies resulted from heterogeneous association of H and L chains derived from HT2 and SU-1-D2 cells.
将两个人杂交瘤细胞系融合以产生杂交抗体。一个人杂交瘤细胞系是HT2,产生对羧肽酶A(Cpase)和双链DNA(ds DNA)有反应的IgM单克隆抗体(MAb),另一个是SU-1-D2,分泌对ds DNA有反应但对Cpase无反应的IgM MAb。通过融合这两种杂交瘤获得的大多数杂交杂交瘤分泌出表现出增强抗原结合强度的杂交抗体。所有对Cpase和ds DNA结合强度增加的杂交抗体仅包含源自SU-1-D2的轻链。这些结果表明,杂交抗体结合强度的增加是由源自HT2和SU-1-D2细胞的重链和轻链的异源缔合导致的。