Gabrilovac J, Pachmann K, Thierfelder S
Blut. 1980 Oct;41(4):269-76. doi: 10.1007/BF01020527.
The kinetics of different cell populations (T and B) and subpopulations (one bearing easily releasable FcR and one bearing stable FcR) was followed in spleens of mice after one single i.p. injection of EAF. The number of FcR bearing cells doubled within 2-7 days after EAF injection. This increase was due to cells bearing temperature sensitive FcR and was accompanied by the doubling of theta positive cells. These results, supported by the demonstration of doubly labeled (theta+FcR+) cells, suggest that EAF injected into normal mice causes the appearance of T-cells expressing easily releasable FcR. These cells, according to Fridman et al. (1977) are suppressor cells. Maximal increase of theta positive cells and of cells with temperature sensitive FcR detected in vitro coincided with the maximum of the suppressive activity of EAF detected in vivo.
在单次腹腔注射艾氏腹水因子(EAF)后,对小鼠脾脏中不同细胞群体(T细胞和B细胞)及其亚群(一个带有易于释放的FcR,另一个带有稳定的FcR)的动力学进行了跟踪研究。在注射EAF后的2 - 7天内,携带FcR的细胞数量增加了一倍。这种增加是由于携带温度敏感型FcR的细胞所致,同时θ阳性细胞数量也增加了一倍。这些结果,通过双标记(θ + FcR +)细胞的证实得到支持,表明注入正常小鼠体内的EAF会导致表达易于释放的FcR的T细胞出现。根据弗里德曼等人(1977年)的研究,这些细胞是抑制细胞。体外检测到的θ阳性细胞和具有温度敏感型FcR的细胞的最大增加量与体内检测到的EAF的最大抑制活性相吻合。