Gardulf Ann, Nicolay Uwe, Asensio Oscar, Bernatowska Ewa, Böck Andreas, Carvalho Beatriz Costa, Granert Carl, Haag Stefan, Hernández Dolores, Kiessling Peter, Kus Jan, Pons Jaune, Niehues Tim, Schmidt Sigune, Schulze Ilka, Borte Michael
Department of Laboratory Medicine, Section of Clinical Immunology, The Swedish Centre for Immunodeficiencies, Karolinska Institutet at Karolinska University Hospital Huddinge, Stockholm, Sweden.
J Clin Immunol. 2006 Mar;26(2):177-85. doi: 10.1007/s10875-006-9002-x. Epub 2006 Apr 26.
Sixty patients (16 children, 44 adults) participated in the study aiming at evaluating: (i) IgG levels when switching patients from intravenous IgG (IVIG) infusions in hospital to subcutaneous (SCIG) self-infusions at home using the same cumulative monthly dose, (ii) protections against infections, and (iii) safety of a new, ready-to-use 16% IgG preparation. All children and 33 adults had received IVIG therapy for >6 months at enrolment. Ten adults who had been on SCIG therapy for many years served as controls. Mean serum IgG trough levels increased in the pre-IVIG children from 7.8 to 9.2 g/L (non-inferiority: p < 0.001) and in the adults from 8.6 to 8.9 g/L (non-inferiority: p < 0.001). Totally 114 respiratory tract infections occurred, 90% of them mild. One serious bacterial infection (pneumonia) was reported for one adult. The annualized rate of serious infections was 0.04 episodes/patient. In total 2297 infusions were given and 28 (1%) systemic adverse reactions occurred, none of them severe. Local tissue reactions declined over time, this being particularly distinct after 8 to 10 weeks. In conclusion, the SCIG administration route was safe. High IgG levels were easily maintained resulting in a very good protection against infections.
60名患者(16名儿童,44名成人)参与了这项旨在评估以下内容的研究:(i)当患者从医院静脉注射免疫球蛋白(IVIG)转为在家自行皮下注射(SCIG)且每月累积剂量相同时的IgG水平;(ii)对感染的防护;(iii)一种新的即用型16%IgG制剂的安全性。所有儿童和33名成人在入组时接受IVIG治疗已超过6个月。10名接受SCIG治疗多年的成人作为对照。IVIG治疗前,儿童的血清IgG谷值水平从7.8 g/L升至9.2 g/L(非劣效性:p < 0.001),成人从8.6 g/L升至8.9 g/L(非劣效性:p < 0.001)。共发生114次呼吸道感染,其中90%为轻度。有一名成人报告发生了一次严重细菌感染(肺炎)。严重感染的年化发生率为0.04次/患者。总共进行了2297次注射,发生了28次(1%)全身不良反应,均不严重。局部组织反应随时间下降,在8至10周后尤为明显。总之,SCIG给药途径是安全的。易于维持高IgG水平,从而对感染有很好的防护作用。