Rapid subcutaneous IgG replacement therapy is effective and safe in children and adults with primary immunodeficiencies -: A prospective, multi-national study

被引:148
作者
Gardulf, Ann
Nicolay, Uwe
Asensio, Oscar
Bernatowska, Ewa
Boeck, Andreas
Costa Carvalho, Beatriz
Granert, Carl
Haag, Stefan
Hernandez, Dolores
Kiessling, Peter
Kus, Jan
Pons, Jaune
Niehues, Tim
Schmidt, Sigune
Schulze, Ilka
Borte, Michael
机构
[1] Karolinska Univ Hosp Huddinge, Dept Lab Med, Sect Clin Immunol, Swedish Ctr Immunodeficiencies,Karolinska Inst, SE-14186 Stockholm, Sweden
[2] Karolinska Univ Hosp Huddinge, Dept Lab Med, Clin Immunol Sect, Karolinska Inst, SE-14186 Stockholm, Sweden
[3] Consorcio Hosp Parc Tauli, Serv Immunol Clin, Sabadell, Spain
[4] Children Mem Hlth Inst, Dept Immunol, Warsaw, Poland
[5] Univ Klin Kinder & Jugendheilkunde, Vienna, Austria
[6] Univ Fed Sao Paulo, Dept Pediat, Div Allergy Clin Immunol & Rheumatol, Sao Paulo, Brazil
[7] Karolinska Univ Hosp Huddinge, Immunodeficiency Unit, Clin Immunol Sect, Stockholm, Sweden
[8] ZLB Behring GmbH, Marburg, Germany
[9] Hosp Univ La Fe, Dept Allergy, Valencia, Spain
[10] Natl Res Inst TB & Lung Dis, Warsaw, Poland
[11] Hosp Univ Son Dureta, Serv Immunol, Palma de Mallorca, Spain
[12] Univ Klinikum Dusseldorf, Klin Kinder Onkol Hamatol & Immunol, Dusseldorf, Germany
[13] Med Univ Klin Freiburg, Abt Rheumatol & Klin Immunol, Freiburg, Germany
[14] Humboldt Univ, Charite Berlin, Klin Padiat Schwerpunkt Pneumol Immunol, Berlin, Germany
[15] Univ Leipzig, Klin Kinder & Jugendmed Stadt Klinikum, Akad Lehrkrankenhaus, D-7010 Leipzig, Germany
关键词
primary antibody deficiency disorders; gammaglobulin treatment; subcutaneous IgG replacement therapy; intravenous IgG replacement therapy;
D O I
10.1007/s10875-006-9002-x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
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页码:177 / 185
页数:9
相关论文
共 32 条
[1]  
Abrahamsen TG, 1996, PEDIATRICS, V98, P1127
[2]  
ADAMS PF, 1996, VITAL HLTH STAT, V10, P1999
[3]  
[Anonymous], 1999, CLIN EXP IMMUNOL, V118, P1
[4]  
Berger M, 2004, INTRAVENOUS IMMUNOGLOBULINS IN THE THIRD MILLENNIUM, P77
[5]   Subcutaneous immunoglobulin replacement in primary immunodeficiencies [J].
Berger, M .
CLINICAL IMMUNOLOGY, 2004, 112 (01) :1-7
[6]  
BJORKANDER J, 1985, INFECTION, V13, P102, DOI 10.1007/BF01642867
[7]   Treatment of patients with primary antibody deficiencies in Germany [J].
Borte, M ;
Oertelt, C ;
Högy, B .
KLINISCHE PADIATRIE, 2005, 217 (05) :276-280
[8]  
BRISTOL DR, 1999, J BIOPHARM STAT, V9, P561
[9]   The comparison of the efficacy and safety of intravenous versus subcutaneous immunoglobulin replacement therapy [J].
Chapel, HM ;
Spickett, GP ;
Ericson, D ;
Engl, W ;
Eibl, MM ;
Bjorkander, J .
JOURNAL OF CLINICAL IMMUNOLOGY, 2000, 20 (02) :94-100
[10]   CONSENSUS ON DIAGNOSIS AND MANAGEMENT OF PRIMARY ANTIBODY DEFICIENCIES [J].
CHAPEL, HM ;
COLE, P ;
GABRIEL, C ;
MILLA, P ;
MORGAN, G ;
SCADDING, G ;
WINFIELD, D ;
BRENNAN, V ;
CARNE, S ;
EWART, H ;
HORN, A ;
JARVIS, F ;
BROWN, D ;
HAENEY, M ;
LEVINSKY, R ;
THOMPSON, R ;
WEBSTER, D ;
WALLINGTON, T .
BRITISH MEDICAL JOURNAL, 1994, 308 (6928) :581-585