Vischer T L
Clin Exp Immunol. 1984 Jan;55(1):99-105.
Mouse spleen cells were cultured for 4 days in RPMI 1640 medium with 5% fetal calf serum. The neutral proteinases trypsin and plasmin, and bacterial lipopolysaccharide LPS, all polyclonal B lymphocyte activators, stimulated the development of immunoglobulin producing cells as detected by the protein A plaque assay. At the same time, direct plaque forming cells reacting with mouse, human and rabbit IgG and the Fc fragment of human IgG were induced by the stimulants. The plaques could be inhibited by free IgG or Fc fragment. In the culture supernatants, IgM and IgM anti-IgG antibodies were detected by enzyme linked immunosorbent assays. Both general IgM and IgM anti-IgG antibodies increased under the influence of the proteinases and of LPS. The results are discussed in relation to rheumatoid factor production during inflammatory diseases.
将小鼠脾细胞在含有5%胎牛血清的RPMI 1640培养基中培养4天。中性蛋白酶胰蛋白酶和纤溶酶以及细菌脂多糖LPS,所有这些多克隆B淋巴细胞激活剂,通过蛋白A空斑试验检测,刺激了产生免疫球蛋白的细胞的发育。同时,刺激剂诱导了与小鼠、人及兔IgG以及人IgG的Fc片段反应的直接空斑形成细胞。这些空斑可被游离的IgG或Fc片段抑制。在培养上清液中,通过酶联免疫吸附测定法检测到IgM和IgM抗IgG抗体。在蛋白酶和LPS的影响下,总IgM和IgM抗IgG抗体均增加。结合炎症性疾病期间类风湿因子的产生对结果进行了讨论。