Gorczynski R M
Immunology. 1974 Jan;26(1):77-95.
The 19S-PFC response to SRBC reaches a peak at 4 days. After this time, the number of 19S-PFC gradually decreases with a half-life of approximately 20 hours. The factors which influence this rate of decline of 19S-PFC after 4 days have been investigated. The decline is not the result of non-specific inhibitors in the tissue medium: medium harvested from cultures at the time of the peak PFC response can support another PFC response by fresh spleen cells. The survival of 19S-PFC in culture is a sensitive function of the number of specific T cells in the culture, since removal of T cells enhances the decline of PFC. Evidence is presented that a θ-negative cell with surface receptors for SRBC can specifically enhance the rate of decay of SRBC-specific 19S-PFC . This decay is mediated by an antigen-specific soluble mediator which cannot be absorbed by specific antigens. This factor is unlikely to be specific hyperimmune mouse IgG since addition of anti-SRBC IgG at 4 days has no affect on the rate of decay of PFC. Although the properties of the supernatant activity have not been characterized, it might be either an anti-receptor antibody or an antigen—antibody complex.
19S-PFC对SRBC的反应在4天时达到峰值。在此之后,19S-PFC的数量逐渐减少,半衰期约为20小时。已经对4天后影响19S-PFC这种下降速率的因素进行了研究。这种下降不是组织培养基中非特异性抑制剂的结果:在PFC反应峰值时从培养物中收获的培养基可以支持新鲜脾细胞的另一次PFC反应。19S-PFC在培养物中的存活是培养物中特异性T细胞数量的敏感函数,因为去除T细胞会加速PFC的下降。有证据表明,一种带有SRBC表面受体的θ阴性细胞可以特异性地加速SRBC特异性19S-PFC的衰变速率。这种衰变是由一种不能被特异性抗原吸收的抗原特异性可溶性介质介导的。这个因子不太可能是特异性超免疫小鼠IgG,因为在4天时添加抗SRBC IgG对PFC的衰变速率没有影响。虽然上清液活性的特性尚未明确,但它可能是一种抗受体抗体或一种抗原-抗体复合物。