Suemura M, Kikutani H, Barsumian E L, Hattori Y, Kishimoto S, Sato R, Maeda A, Nakamura H, Owaki H, Hardy R R
J Immunol. 1986 Aug 15;137(4):1214-20.
Three monoclonal antibodies, 1-7 (gamma 2b), 3-5 (gamma 1), and 8-30 (mu), specific to Fc epsilon receptors (Fc epsilon R) on human B cells were established. The two monoclonals (1-7 and 8-30) could inhibit the binding of IgE to Fc epsilon R in rosette formation assays, as well as FACS analysis, and were shown to recognize the same epitope of Fc epsilon R. The other monoclonal antibody (3-5) recognized the same molecule but a different epitope, and marginally inhibited the IgE binding. The molecules on RPMI 8866 cells recognized by these monoclonal antibodies had Mr of 46,000 and 25,000 to 30,000 daltons as determined by immunoprecipitation and SDS-PAGE analysis. By employing these monoclonal antibodies, the expression of Fc epsilon R on circulating lymphocytes was studied. Approximately 50% of B cells from normal, nonatopic individuals were found to express Fc epsilon R, and a remarkable increase in the expression of Fc epsilon R was observed in B cells of atopic patients. The expression of Fc epsilon R was not detected in T cells from atopic patients (including hyper IgE syndrome) as well as normal individuals. Incubation of B cells with PHA-conditioned medium plus IgE augmented the expression of Fc epsilon R in the Fc epsilon R+ B cell population but not in Fc epsilon R- population. PHA-conditioned medium plus IgE did not induce Fc epsilon R expression on T cells.
制备了三种针对人B细胞上Fcε受体(FcεR)的单克隆抗体,分别为1-7(γ2b)、3-5(γ1)和8-30(μ)。在玫瑰花环形成试验以及流式细胞术分析中,两种单克隆抗体(1-7和8-30)能够抑制IgE与FcεR的结合,并且显示它们识别FcεR的相同表位。另一种单克隆抗体(3-5)识别相同分子但不同表位,对IgE结合仅有轻微抑制作用。通过免疫沉淀和SDS-PAGE分析确定,这些单克隆抗体识别的RPMI 8866细胞上的分子分子量分别为46,000以及25,000至30,000道尔顿。利用这些单克隆抗体,对循环淋巴细胞上FcεR的表达进行了研究。发现正常非特应性个体中约50%的B细胞表达FcεR,而在特应性患者的B细胞中观察到FcεR表达显著增加。在特应性患者(包括高IgE综合征)以及正常个体的T细胞中未检测到FcεR的表达。用PHA条件培养基加IgE孵育B细胞,可增强FcεR+B细胞群体中FcεR的表达,但在FcεR-群体中则无此作用。PHA条件培养基加IgE未诱导T细胞上FcεR的表达。