Bona C, Audibert F, Juy D, Chedid L
Clin Exp Immunol. 1976 Nov;26(2):258-66.
Secific stimulation of T-cells by PPD was inhibited by their autologous B cells. This inhibition was obtained with B cells separated either by depletion of E-RFC or by elution, with human IgG of lymphocytes bound to Sephadex beads coated with rabbit antibodies anti-human Fab fragments. The suppression was proportional to the number of B cells added to 10(6) T cells incubated with PPD and as previously reported was more marked in the case of B or T cells from BCG-vaccinated subjects with negative skin tests. The suppressive phenomenon required viable B cells and was inhibited by cycloheximide but was not altered by pretreatment of suppressor cells with actinomycin D or colchicine. It seems that B-suppressor cells interfere with recognition of PPD by T cells rather than with the proliferative phase of the specific blast response. Using various surface markers (i.e. Ig, C3 and Fc receptors) it was shown that the suppressor cells represent a subset of Ig-bearing B cells which do not carry Fc receptors.
结核菌素纯蛋白衍生物(PPD)对T细胞的特异性刺激受到其自身B细胞的抑制。这种抑制作用在通过去除E受体阳性(E-RFC)细胞或洗脱法分离得到的B细胞中均能观察到,洗脱法是使用结合于包被有抗人Fab片段兔抗体的葡聚糖凝胶珠上的人IgG来洗脱淋巴细胞。抑制作用与加入到与PPD共同孵育的10⁶个T细胞中的B细胞数量成正比,并且如先前报道的那样,在结核菌素皮肤试验阴性的卡介苗接种受试者的B细胞或T细胞中更为明显。抑制现象需要有活力的B细胞,并且受到放线菌酮的抑制,但用放线菌素D或秋水仙碱预处理抑制细胞不会改变这种抑制作用。似乎B抑制细胞干扰T细胞对PPD的识别,而不是干扰特异性母细胞反应的增殖阶段。使用各种表面标志物(即Ig、C3和Fc受体)表明,抑制细胞代表了一类带有Ig但不携带Fc受体的B细胞亚群。