Tsang V C, Hancock K, Maddison S E, Beatty A L, Moss D M
J Immunol. 1984 May;132(5):2607-13.
Analysis of human serum reactivities to the Schistosoma mansoni adult microsomal antigens (MAMA) showed that S. japonicum and S. haematobium infection sera, as a rule, did not react as well to MAMA as did the homologous S. mansoni infection sera. The degree of species specificity, although not absolute, was quite pronounced. Purification of the corresponding microsomal antigens from S. japonicum adults (JAMA) and subsequent assays with both homologous and heterologous infection sera show a distinct and reciprocating species specificity between S. mansoni and S. japonicum microsomal antigens. The specificities of these antigens were quantitated by k-ELISA. Qualitative analysis of active antigenic components for both JAMA and MAMA involved assay by the "Western blot" or enzyme-linked immunoelectrotransfer blot (EITB). The EITB patterns of both antigens, after resolution by SDS-PAGE, show species-specific reactive bands at the 16,000 to 35,000 m.w. region. S. japonicum-specific antigens are located at the 18,000 to 35,000 m.w. region whereas S. mansoni-specific antigens were associated with m.w. components of 16,000 to 29,000. High m.w. antigen components (greater than 40,000) of both JAMA and MAMA are recognized by both heterologous and homologous infection sera and are thus not species specific. The demonstration of the clear separation of species-specific antigen bands of JAMA and MAMA by physical size offers a unique opportunity to isolate and characterize the species specificities of antibody-antigen reactions in these parasitic infections.
对人血清与曼氏血吸虫成虫微粒体抗原(MAMA)反应性的分析表明,日本血吸虫和埃及血吸虫感染血清通常对MAMA的反应不如同源的曼氏血吸虫感染血清。物种特异性程度虽非绝对,但相当明显。从日本血吸虫成虫中纯化相应的微粒体抗原(JAMA),随后用同源和异源感染血清进行检测,结果显示曼氏血吸虫和日本血吸虫微粒体抗原之间存在明显的相互物种特异性。这些抗原的特异性通过k-ELISA进行定量。对JAMA和MAMA活性抗原成分的定性分析采用“免疫印迹法”或酶联免疫电转移印迹法(EITB)。两种抗原经SDS-PAGE分离后的EITB图谱显示,在分子量16,000至35,000区域存在物种特异性反应条带。日本血吸虫特异性抗原位于分子量18,000至35,000区域,而曼氏血吸虫特异性抗原与分子量16,000至29,000的成分相关。JAMA和MAMA的高分子量抗原成分(大于40,000)可被异源和同源感染血清识别,因此不是物种特异性的。通过物理大小明确分离JAMA和MAMA的物种特异性抗原条带,为分离和鉴定这些寄生虫感染中抗体-抗原反应的物种特异性提供了独特机会。