Spencer H C, Collins W E, Stanfill P S, Huong A Y, Barber A M, Contacos P G
Am J Trop Med Hyg. 1981 Mar;30(2):358-63. doi: 10.4269/ajtmh.1981.30.358.
Sequentially collected sera from Mongolian jirds (Meriones unguiculatus) infected with Brugia malayi and B. pahangi were tested for antibodies to homologous and heterologous antigens by the enzyme-linked immunosorbent assay (ELISA). Titers were less than 1:100 prior to infection and rose rapidly (within 2 weeks). Peak titers were observed prior to patent microfilaremia, and high titers persisted during infection. Use of the homologous antigen did not increase sensitivity or specificity of the ELISA. In fact, B. malayi-infected jirds demonstrated higher titers to the heterologous antigen, B. pahangi, than to the homologous antigen. Fractionation of B. malayi antigen over a wide pH range using isoelectric focusing did not eliminate cross-reactions, but the reactions of 20 B. malayi sera and 20 B. pahangi sera tested more strongly to specific fractions, particularly in the lower pH range.
对感染马来布鲁线虫和彭亨布鲁线虫的长爪沙鼠(Meriones unguiculatus)依次采集的血清,采用酶联免疫吸附测定(ELISA)检测针对同源和异源抗原的抗体。感染前滴度低于1:100,且迅速上升(2周内)。在出现明显微丝蚴血症之前观察到峰值滴度,且在感染期间高滴度持续存在。使用同源抗原并未提高ELISA的敏感性或特异性。事实上,感染马来布鲁线虫的长爪沙鼠对异源抗原彭亨布鲁线虫的滴度高于对同源抗原的滴度。使用等电聚焦在较宽pH范围内对马来布鲁线虫抗原进行分级分离并未消除交叉反应,但20份感染马来布鲁线虫的血清和20份感染彭亨布鲁线虫的血清对特定级分反应更强,尤其是在较低pH范围内。