Vadiee A R, Shannon E J, Gillis T P, Hastings R C
Immunology Research Department, GWL Hansen's Disease Center, Carville, Louisiana 70721.
Int J Lepr Other Mycobact Dis. 1988 Jun;56(2):274-82.
Armadillo IgG and IgM antibody responses to Mycobacterium leprae were analyzed using isotypic-specific antisera by means of immunoblotting. Blots developed for IgG antibodies to M. leprae showed multiple protein antigens (Mr = 12-90 K) in some heavily infected armadillos. In contrast, blots developed for IgM antibodies to M. leprae showed a single, broad, diffuse band of immunoreactivity at approximately 33 kDa. The 33-kDa immunogen was detectable with silver stain modified for carbohydrate reactivity, suggesting the presence of a polysaccharide component. In addition, binding of 125I-concanavalin A to the 33-kDa component demonstrated the presence of mannose and/or glucose residues.
利用同型特异性抗血清,通过免疫印迹法分析犰狳针对麻风分枝杆菌的IgG和IgM抗体反应。针对麻风分枝杆菌IgG抗体显影的印迹在一些重度感染的犰狳中显示出多种蛋白质抗原(分子量=12 - 90K)。相比之下,针对麻风分枝杆菌IgM抗体显影的印迹在约33kDa处显示出一条单一、宽阔、弥散的免疫反应带。用针对碳水化合物反应性改良的银染法可检测到33kDa的免疫原,提示存在多糖成分。此外,125I-伴刀豆球蛋白A与33kDa成分的结合证明存在甘露糖和/或葡萄糖残基。