Chitnis N D, Hegde U C
Institute for Research in Reproduction, Bombay.
Indian J Med Res. 1990 Aug;92:267-72.
Two groups of adult Swiss mice were immunised with washed syngeneic spermatozoa without any adjuvant for a period of two months or four months respectively. The presence of antibodies to spermatozoa was measured by micro sperm-agglutination and micro sperm-immobilization tests. The development of cell mediated immune response (CMIR) was measured by leucocyte migration inhibition test (LMIT) using spermatozoal antigens solubilized by 3M KCl, Nonidet P-40 or by subjecting the cells to ultrasonication. SDS-PAGE analysis of these proteins indicated that extraction of spermatozoa with 3 M KCl was a better method for solubilization of antigens present on sperm membrane. Almost all immunized mice had varying titers of sperm agglutinating antibodies. Nearly 40-50 per cent of the mice had a titre of 1:128 in both groups whereas only 33 per cent had sperm immobilizing antibodies. CMIR, as assessed by LMIT, was detected in immunized mice. However, this had not resulted in the infiltration of immune cells into the target organs perhaps due to the lower magnitude of immune response.
将两组成年瑞士小鼠分别用未添加任何佐剂的同种异体洗涤精子免疫两个月或四个月。通过微量精子凝集试验和微量精子制动试验检测精子抗体的存在。使用经3M KCl、NP-40溶解的精子抗原或对细胞进行超声处理,通过白细胞迁移抑制试验(LMIT)检测细胞介导免疫反应(CMIR)的发展。对这些蛋白质进行的SDS-PAGE分析表明,用3M KCl提取精子是溶解精子膜上抗原的更好方法。几乎所有免疫小鼠都有不同滴度的精子凝集抗体。两组中近40%-50%的小鼠滴度为1:128,而只有33%的小鼠有精子制动抗体。通过LMIT评估,在免疫小鼠中检测到CMIR。然而,这可能由于免疫反应程度较低,并未导致免疫细胞浸润到靶器官。