Berger C, Gratwohl A, Doran J E, Scherz R, Baumgartner C, Morell A, Bachmann B, Spaeth P J, Tichelli A, Speck B
Abteilung für Hämatologie, Kantonsspital Basel.
Beitr Infusionsther. 1989;24:112-21.
Ten consecutive bone marrow transplant recipients were assigned alternatively to receive either a high dose polyspecific intravenous immunglobulin (HDIVIG) 0.5 g/kg weekly X 14, or a conventional dose of a CMV specific intravenous immunglobulin (CMVIG) 0.1 g/kg every three weeks. Before and after each application we determined the levels of total IgG, IgG subclasses, IgG 1, IgG 2, IgG 3, IgG 4, total IgA and IgM and of specific IgG and IgM antibody concentrations against endotoxin, lipid A, streptococcus A, hemophilus, EBV and CMV. In the HDIVIG, total IgG rose from 11 (median, range 2-11) g/l to 25 (22-32) g/l by day 89, in the CMVIG group, IgG dropped from 11 (10-15) g/l to 9 (6-12) g/l. In the same period the mean levels of IgG subclasses expressed as % of normal plasma pool increased in the HDIVIG group in all subclasses, not in the CMVIG group. The differences were significant, however, only for IgG 1 and IgG 2. IgG-antibodies against CMV, EBV, endotoxin, streptococcus and hemophilus did increase significantly in the HDIVIG group, but not in the CMVIG group. No increase was seen in both groups in lipid A antibodies and in specific IgM antibodies. Each application of CMVIG induced a transient increase of anti-CMV antibodies. We conclude that HDIVIG induces reproducibly an increase of specific and non-specific IgG antibodies. No attempt was made to assess clinical outcome. However, these results provide a rational basis for further therapeutic studies.
一是每周静脉注射高剂量多特异性免疫球蛋白(HDIVIG)0.5 g/kg,共14周;二是每三周静脉注射常规剂量的巨细胞病毒特异性免疫球蛋白(CMVIG)0.1 g/kg。在每次用药前后,我们测定了总IgG、IgG亚类、IgG1、IgG2、IgG3、IgG4、总IgA和IgM的水平,以及针对内毒素、脂多糖A、A组链球菌、嗜血杆菌、EB病毒和巨细胞病毒的特异性IgG和IgM抗体浓度。在HDIVIG组中,到第89天时,总IgG从11(中位数,范围2 - 11)g/l升至25(22 - 32)g/l,而在CMVIG组中,IgG从11(10 - 15)g/l降至9(6 - 12)g/l。同期,HDIVIG组中所有亚类的IgG亚类以正常血浆池百分比表示的平均水平均升高,而CMVIG组未升高。不过,差异仅在IgG1和IgG2方面具有统计学意义。HDIVIG组中针对巨细胞病毒、EB病毒、内毒素、链球菌和嗜血杆菌的IgG抗体显著增加,而CMVIG组未增加。两组中脂多糖A抗体和特异性IgM抗体均未见增加。每次应用CMVIG均诱导抗巨细胞病毒抗体短暂增加。我们得出结论,HDIVIG可重复性地诱导特异性和非特异性IgG抗体增加。本研究未尝试评估临床结局。然而,这些结果为进一步的治疗研究提供了合理依据。