Möller G
Folia Microbiol (Praha). 1985;30(3):203-11. doi: 10.1007/BF02923512.
The enzyme dextranase could degrade antigenic dextran in vivo even when given 6-15 d after the antigen. Dextranase injected after the antigen suppressed the immune response when given 24 but not 48 h after the antigen, indicating that the antigen must interact with the immune system for 48 h to initiate a response. Thereafter, the B cells are independent of further antigen stimulation. To show whether antibody-mediated suppression of the immune response was determinant specific FITC-conjugated SRC were applied as immunogen and antibodies were raised both against the carrier (SRC) and the FITC hapten. When these antibodies were injected 1-3 h after the immunogen they only suppressed the immune response to the corresponding determinant. Anti-carrier antibodies usually enhanced the response to the hapten. Therefore, antibody-mediated suppression of the immune response is determinant-specific and cannot be mediated in vivo to a detectable extent by the Fc part of the antibodies.
即使在抗原注射6 - 15天后给予,葡聚糖酶也能在体内降解抗原性葡聚糖。抗原注射后24小时而非48小时给予葡聚糖酶,可抑制免疫反应,这表明抗原必须与免疫系统相互作用48小时才能启动反应。此后,B细胞不再依赖进一步的抗原刺激。为了表明抗体介导的免疫反应抑制是否具有决定簇特异性,将异硫氰酸荧光素(FITC)偶联的血清白蛋白(SRC)用作免疫原,并产生针对载体(SRC)和FITC半抗原的抗体。当在免疫原注射后1 - 3小时注射这些抗体时,它们仅抑制对相应决定簇的免疫反应。抗载体抗体通常会增强对半抗原的反应。因此,抗体介导的免疫反应抑制具有决定簇特异性,并且在体内抗体的Fc部分无法介导到可检测的程度。