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普通可变免疫缺陷患者皮下输注后γ-球蛋白的生物利用度。

Bioavailability of gamma-globulin after subcutaneous infusions in patients with common variable immunodeficiency.

作者信息

Waniewski J, Gardulf A, Hammarström L

机构信息

Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, Warsaw.

出版信息

J Clin Immunol. 1994 Mar;14(2):90-7. doi: 10.1007/BF01541341.

Abstract

Replacement therapy, using subcutaneous infusions of gamma-globulin, is being applied increasingly for antibody-deficient patients, as this form of treatment has been found to be related to a very low frequency of adverse systemic reactions. However, the uptake of IgG from subcutaneous tissue may be low, owing to degradation locally, especially for the IgG3 molecule. Therefore, the kinetics of IgG and IgG-subclass concentrations in the sera of 23 patients with common variable immunodeficiency was investigated during 18 months of subcutaneous infusions of gamma-globulin (100 mg/kg/week). Seventeen patients were previously treated with intramuscular injections or intravenous infusions. The mean serum IgG level increased twice in the previously treated patients and four times in the previously untreated patients. A steady state was reached after 6 months if the subcutaneous infusions were given weekly and after 1 week if the patients were given daily infusions for 5 consecutive days and, thereafter, weekly infusions. The fractional catabolic rate of IgG (4.1-5.9% per day) was found to be at the lower limit reported for normal controls, if 100% bioavailability of the infused IgG was assumed. The fractional contents of IgG subclasses in the patients' serum IgG resembled the physiological pattern, with the exception of IgG4, which was not present in the gamma-globulin preparations used. Significantly increased levels of IgG1 and -2 were seen in both previously treated and untreated patients during the treatment.

摘要

对于抗体缺陷患者,使用皮下注射γ-球蛋白的替代疗法应用越来越广泛,因为已发现这种治疗形式与极低的全身性不良反应发生率相关。然而,由于局部降解,尤其是对于IgG3分子,皮下组织中IgG的摄取可能较低。因此,在23例常见可变免疫缺陷患者皮下注射γ-球蛋白(100mg/kg/周)的18个月期间,对其血清中IgG和IgG亚类浓度的动力学进行了研究。17例患者先前接受过肌肉注射或静脉输注治疗。先前接受治疗的患者血清IgG平均水平升高了两倍,而先前未接受治疗的患者升高了四倍。如果每周进行皮下注射,6个月后达到稳态;如果患者连续5天每天进行注射,之后每周注射,则1周后达到稳态。如果假设注入的IgG生物利用度为100%,则发现IgG的分解代谢率(每天4.1-5.9%)处于正常对照报道的下限。患者血清IgG中IgG亚类的相对含量与生理模式相似,但所用γ-球蛋白制剂中不存在的IgG4除外。在治疗期间,先前接受治疗和未接受治疗的患者中IgG1和IgG2水平均显著升高。

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