Viyanant V, Sobhon P, Upatham E S
Department of Biology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Parasite Immunol. 1994 Apr;16(4):221-3. doi: 10.1111/j.1365-3024.1994.tb00343.x.
A panel of monoclonal antibodies (MoAbs) against freeze-thaw surface tegumental antigens of Schistosoma mekongi were produced from naturally infected BALB/c mice. In this study, we have characterized two MoAbs which have different antigenic specificity for S. mekongi, S. japonicum and S. mansoni. The target epitopes of these two hybridoma antibodies are contained in the M(r) 38 kDa (designated Sme 38) and M(r) 97 kDa (designated Sme 97) proteins of adult worms as analysed by immunoblotting. The Sme 38 epitope was genus-specific, since it is also detectable in S. japonicum and S. mansoni. The Sme 97 was not detected in S. japonicum and S. mansoni, therefore it is considered as species-specific epitope. Immunocytochemical analysis revealed the presence of Sme 38 epitope in the surface tegument, the tegumental cells lying underneath the muscle layer and gut surface. The Sme 97 epitope was detectable only in the surface tegumental area.
利用自然感染的BALB/c小鼠制备了一组针对湄公血吸虫冻融表面皮层抗原的单克隆抗体(MoAbs)。在本研究中,我们鉴定了两种对湄公血吸虫、日本血吸虫和曼氏血吸虫具有不同抗原特异性的单克隆抗体。通过免疫印迹分析,这两种杂交瘤抗体的靶表位分别包含在成虫的分子量为38 kDa(命名为Sme 38)和97 kDa(命名为Sme 97)的蛋白质中。Sme 38表位具有属特异性,因为在日本血吸虫和曼氏血吸虫中也能检测到。在日本血吸虫和曼氏血吸虫中未检测到Sme 97,因此它被认为是种特异性表位。免疫细胞化学分析显示,Sme 38表位存在于表面皮层、肌肉层下方的皮层细胞和肠道表面。Sme 97表位仅在表面皮层区域可检测到。