Tani K, Sakamoto H, Katoh K, Matsunagai K, Yamada S, Okuda K, Handwerger B S
Rheumatol Int. 1986;6(1):19-24. doi: 10.1007/BF00270660.
Autoantibody-secreting hybrid cell lines were obtained by fusion of spleen cells from unimmunized (NZB X NZW) F1 mice with the HAT-sensitive mouse myeloma cell line SP2/0-Ag14. Eight hybridoma cell lines producing autoantibodies to mouse thymocytes were cloned and the resultant antibodies were partially characterized. All eight monoclonal antibodies lysed mouse thymocytes in the presence of rabbit complement. The anti-thymocyte cytotoxic antibody activities were absorbed with thymocytes, lymph node cells, unfractionated spleen cells, and splenic T cells; but not with bone marrow cells, splenic B cells, or homogenates of mouse kidney, liver, or striated muscle cells. In addition, the cytotoxic activities of culture supernatants from seven of the eight hybrid clones were absorbed with mouse brain tissue homogenates. Isotyping of the monoclonal antibodies revealed that five were IgM and three were IgG2a. Mouse thymocytes sensitized with each of the eight monoclonal antibodies in vitro became highly susceptible to phagocytosis by syngeneic macrophages. The monoclonal antithymocyte antibodies, thus, appear to be similar to the naturally occurring, (NZB X NZW) F1 thymocytotoxic autoantibodies (NTA) described by Shirai et al.
通过将未免疫的(新西兰黑鼠×新西兰白鼠)F1小鼠的脾细胞与对次黄嘌呤-氨基蝶呤-胸腺嘧啶核苷(HAT)敏感的小鼠骨髓瘤细胞系SP2/0-Ag14融合,获得了分泌自身抗体的杂交细胞系。克隆了8个产生抗小鼠胸腺细胞自身抗体的杂交瘤细胞系,并对所得抗体进行了部分特性鉴定。所有8种单克隆抗体在兔补体存在的情况下均能裂解小鼠胸腺细胞。抗胸腺细胞细胞毒性抗体活性可被胸腺细胞、淋巴结细胞、未分离的脾细胞和脾T细胞吸收;但不能被骨髓细胞、脾B细胞或小鼠肾脏、肝脏或横纹肌细胞的匀浆吸收。此外,8个杂交克隆中有7个的培养上清液的细胞毒性活性可被小鼠脑组织匀浆吸收。单克隆抗体的分型显示,5种为IgM,3种为IgG2a。用8种单克隆抗体中的每一种在体外致敏的小鼠胸腺细胞对同基因巨噬细胞的吞噬作用变得高度敏感。因此,单克隆抗胸腺细胞抗体似乎与Shirai等人描述的天然存在的(新西兰黑鼠×新西兰白鼠)F1胸腺细胞毒性自身抗体(NTA)相似。