Samarut C, Brochier J, Fridman W H, Revillard J P
Eur J Immunol. 1980 Nov;10(11):894-8. doi: 10.1002/eji.1830101116.
Soluble receptors for FcIgG released from unstimulated human peripheral blood lymphocytes were isolated by affinity chromatography on Sepharose 4B-IgG. This material was shown to interfere with the differentiation of peripheral blood B cells into Ig-secreting cells in cultures stimulated with pokeweek or Nocardia opaca extracts. Neither cell viability nor [3H]thymidine incorporation were altered, but the number of Ig-containing cells and that of Ig-secreting cells were decreased. These effects were dose-related. They were found to be associated with Fc IgG-binding soluble material, since absorption on Sepharose 4B-IgG but not on pepsin-digested F(ab')2 fragments removed the inhibitory activity. This suppressor factor, released by unstimulated lymphocytes, may represent a human analogue of murine immunoglobulin-binding factor (IBF) produced by alloactivated T cells.
通过在琼脂糖4B-免疫球蛋白G(Sepharose 4B-IgG)上进行亲和层析,从未受刺激的人外周血淋巴细胞中分离出FcIgG的可溶性受体。已证明该物质会干扰在用商陆或暗色诺卡氏菌提取物刺激的培养物中,外周血B细胞分化为分泌免疫球蛋白的细胞。细胞活力和[3H]胸苷掺入均未改变,但含免疫球蛋白的细胞数量和分泌免疫球蛋白的细胞数量减少。这些作用与剂量相关。发现它们与Fc IgG结合可溶性物质有关,因为在琼脂糖4B-IgG上而非胃蛋白酶消化的F(ab')2片段上的吸附消除了抑制活性。这种由未受刺激的淋巴细胞释放的抑制因子,可能代表同种异体活化T细胞产生的小鼠免疫球蛋白结合因子(IBF)的人类类似物。