Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor.

Treatment of common variable immunodeficiency disorders (CVID) is based on replacement therapy using intravenous (i.v.) or subcutaneous (s.c.) immunoglobulin (Ig)G. Interindividual variation of IgG dose is common. A total of 380 CVID patients on stable IgG replacement from two prospective cohorts we...

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Main Authors: Gouilleux-Gruart, V, Chapel, H, Chevret, S, Lucas, M, Malphettes, M, Fieschi, C, Patel, S, Boutboul, D, Marson, M, Gérard, L, Lee, M, Watier, H, Oksenhendler, E
Format: Journal article
Language:English
Published: 2013
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author Gouilleux-Gruart, V
Chapel, H
Chevret, S
Lucas, M
Malphettes, M
Fieschi, C
Patel, S
Boutboul, D
Marson, M
Gérard, L
Lee, M
Watier, H
Oksenhendler, E
author_facet Gouilleux-Gruart, V
Chapel, H
Chevret, S
Lucas, M
Malphettes, M
Fieschi, C
Patel, S
Boutboul, D
Marson, M
Gérard, L
Lee, M
Watier, H
Oksenhendler, E
author_sort Gouilleux-Gruart, V
collection OXFORD
description Treatment of common variable immunodeficiency disorders (CVID) is based on replacement therapy using intravenous (i.v.) or subcutaneous (s.c.) immunoglobulin (Ig)G. Interindividual variation of IgG dose is common. A total of 380 CVID patients on stable IgG replacement from two prospective cohorts were analysed. An 'efficiency' index was defined as the ratio of serum IgG trough level minus IgG residual to the average weekly dose of IgG infusion. A reduced efficiency of IgG was associated independently with the i.v. route (P < 0·001) and with the presence of at least one CVID disease-related phenotype (lymphoproliferation, autoimmune cytopenia or enteropathy) (P < 0·001). High IgG efficiency was noted in patients homozygotes for the variable number tandem repeat (VNTR) 3/3 polymorphism of the neonatal Fc receptor gene [IgG Fc fragment receptor transporter alpha chain (FCGRT)] promoter, and this was particularly significant in patients treated with IVIG (P < 0.01). In a multivariate analysis, FCGRT VNTR 3/3 genotype (P = 0·008) and high serum albumin (P < 0·001) were associated independently with increased efficiency of i.v. Ig.
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spelling oxford-uuid:cb5ae0b7-5f61-4084-8192-5f8aecb130672022-03-27T07:14:16ZEfficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:cb5ae0b7-5f61-4084-8192-5f8aecb13067EnglishSymplectic Elements at Oxford2013Gouilleux-Gruart, VChapel, HChevret, SLucas, MMalphettes, MFieschi, CPatel, SBoutboul, DMarson, MGérard, LLee, MWatier, HOksenhendler, ETreatment of common variable immunodeficiency disorders (CVID) is based on replacement therapy using intravenous (i.v.) or subcutaneous (s.c.) immunoglobulin (Ig)G. Interindividual variation of IgG dose is common. A total of 380 CVID patients on stable IgG replacement from two prospective cohorts were analysed. An 'efficiency' index was defined as the ratio of serum IgG trough level minus IgG residual to the average weekly dose of IgG infusion. A reduced efficiency of IgG was associated independently with the i.v. route (P < 0·001) and with the presence of at least one CVID disease-related phenotype (lymphoproliferation, autoimmune cytopenia or enteropathy) (P < 0·001). High IgG efficiency was noted in patients homozygotes for the variable number tandem repeat (VNTR) 3/3 polymorphism of the neonatal Fc receptor gene [IgG Fc fragment receptor transporter alpha chain (FCGRT)] promoter, and this was particularly significant in patients treated with IVIG (P < 0.01). In a multivariate analysis, FCGRT VNTR 3/3 genotype (P = 0·008) and high serum albumin (P < 0·001) were associated independently with increased efficiency of i.v. Ig.
spellingShingle Gouilleux-Gruart, V
Chapel, H
Chevret, S
Lucas, M
Malphettes, M
Fieschi, C
Patel, S
Boutboul, D
Marson, M
Gérard, L
Lee, M
Watier, H
Oksenhendler, E
Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor.
title Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor.
title_full Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor.
title_fullStr Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor.
title_full_unstemmed Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor.
title_short Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor.
title_sort efficiency of immunoglobulin g replacement therapy in common variable immunodeficiency correlations with clinical phenotype and polymorphism of the neonatal fc receptor
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