Wu Q X
Institute of Dermatology, CAMS, Nanjing.
Zhonghua Yi Xue Za Zhi. 1992 Nov;72(11):683-5, 703.
A series of hybridoma cell lines, which secrete monoclonal antibodies (McAbs), were produced by means of fusion between mouse myeloma cells SP2/O and spleen cells from BALB/C mice immunized with whole M. leprae plus unique phenolic glycolipid I(PGL-I) of M. leprae and M. leprae sonicates supernatant fluid (MLSS) as immunogen. Primary identification indicated that H2 cell line can secrete McAb against the epitope of PGL-I; IIIE10 cell line can secrete McAb against PGL-I and MLSS and (5) 24 D6C8 cell line only against whole M. leprae. The uses of these McAbs in serodiagnosis of leprosy, identification of M. leprae, analysis and purification of M. leprae antigens, and key problems in technology for producing McAbs against M. leprae were also discussed.
通过将小鼠骨髓瘤细胞SP2/O与用完整麻风杆菌加麻风杆菌独特的酚糖脂I(PGL-I)和麻风杆菌超声破碎上清液(MLSS)作为免疫原免疫的BALB/C小鼠的脾细胞进行融合,产生了一系列分泌单克隆抗体(McAbs)的杂交瘤细胞系。初步鉴定表明,H2细胞系可分泌针对PGL-I表位的单克隆抗体;IIIE10细胞系可分泌针对PGL-I和MLSS的单克隆抗体,而24 D6C8细胞系仅针对完整的麻风杆菌。还讨论了这些单克隆抗体在麻风病血清诊断、麻风杆菌鉴定、麻风杆菌抗原分析与纯化中的应用以及制备抗麻风杆菌单克隆抗体技术中的关键问题。