Kabelitz D, Janssen O
Department of Medical Microbiology and Immunology, University of Ulm, Federal Republic of Germany.
Cell Immunol. 1989 Apr 15;120(1):21-30. doi: 10.1016/0008-8749(89)90171-8.
Among five anti-HLA class II monoclonal antibodies (mab's) tested, the anti-HLA-DR mab L243 selectively inhibited the in vitro proliferation of Epstein-Barr virus-transformed lymphoblastoid cell lines (LCL). Saturating amounts of L243 mab induced 50% suppression of LCL growth as revealed by measuring [3H]thymidine incorporation or counting cell numbers. Preincubation for 20 hr at 37 degrees C in the presence of L243 mab dramatically reduced the expression of certain B cell-specific antigens on LCL, notably CD23 (BLAST-2, low affinity Fc epsilon receptor). In view of the known function of the CD23 antigen as a B cell growth factor receptor, we discuss the possibility that the suppressive effect of L243 mab on LCL proliferation is due to down-regulation of CD23 antigen expression.
在所测试的五种抗人白细胞抗原(HLA)Ⅱ类单克隆抗体(mab)中,抗HLA - DR单克隆抗体L243能选择性抑制爱泼斯坦 - 巴尔病毒(Epstein - Barr virus)转化的淋巴母细胞系(LCL)的体外增殖。通过测量[³H]胸腺嘧啶核苷掺入量或计数细胞数量发现,饱和量的L243单克隆抗体可使LCL生长受到50%的抑制。在L243单克隆抗体存在的情况下,于37℃预孵育20小时,可显著降低LCL上某些B细胞特异性抗原的表达,尤其是CD23(BLAST - 2,低亲和力Fcε受体)。鉴于已知CD23抗原作为B细胞生长因子受体的功能,我们讨论了L243单克隆抗体对LCL增殖的抑制作用可能是由于CD23抗原表达下调的可能性。