Leickley F E, Buckley R
Clin Exp Immunol. 1986 Jul;65(1):90-9.
Among seven males with X-linked agammaglobulinemia in an extended pedigree, serum immunoglobulins and antibodies were extremely low in all but one who had a normal IgA (78 mg/dl) and tetanus antibodies (1:19,683). Following bacteriophage phi X 174 immunizations, the oldest failed to clear phage and had no primary or secondary antibody responses. The youngest had normal phage clearance, low primary and secondary antibody responses, and no amplification or switching to IgG. The other four affected had normal or slightly delayed phage clearance, low primary and secondary responses, but some amplification and switching from IgM to IgG which increased with age. Normal percentages of surface immunoglobulin positive cells were present in the two youngest patients, but all seven affected had very low percentages of cells reacting with monoclonal antibodies to B cell surface antigens. Immunoglobulin production by cultured blood B cells was very low and not increased by pokeweed mitogen. However, a majority of Epstein-Barr virus (EBV)-transformed lymphoblastoid cells derived from the blood of four of the patients bore IgD and IgM and reacted with all of the monoclonal antibodies to B cell antigens. Culture supernatants from those lines contained significant quantities of IgM and lesser amounts of IgG and IgA. The studies presented here provide further support for the hypothesis that the primary abnormality in X-linked agammaglobulinemia affects B cells at more than one stage of development rather than just at the level of the pre-B cell.
在一个大家族中患有X连锁无丙种球蛋白血症的7名男性中,除1人IgA正常(78mg/dl)且破伤风抗体正常(1:19,683)外,其余所有人的血清免疫球蛋白和抗体水平都极低。在接种噬菌体φX 174后,最年长的患者无法清除噬菌体,且无初次或二次抗体应答。最年轻的患者噬菌体清除正常,初次和二次抗体应答较低,且无IgG的扩增或类别转换。其他4名患者噬菌体清除正常或略有延迟,初次和二次应答较低,但有一些从IgM到IgG的扩增和类别转换,且随年龄增长而增加。最年轻的两名患者表面免疫球蛋白阳性细胞百分比正常,但所有7名患者中与B细胞表面抗原单克隆抗体反应的细胞百分比都非常低。培养的血液B细胞产生的免疫球蛋白非常低,且美洲商陆丝裂原不能使其增加。然而,来自4名患者血液的大多数爱泼斯坦-巴尔病毒(EBV)转化的淋巴母细胞系带有IgD和IgM,并与所有B细胞抗原单克隆抗体发生反应。这些细胞系的培养上清液含有大量IgM以及少量IgG和IgA。本文所呈现的研究进一步支持了以下假说:X连锁无丙种球蛋白血症的原发性异常在B细胞发育的多个阶段产生影响,而非仅在前B细胞水平。