Evidence map›Paper›PMID 23286945›Full record

ArticleClinical and experimental immunology2013

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

V Gouilleux-Gruart, H Chapel, S Chevret, M Lucas, M Malphettes, C Fieschi, S Patel, D Boutboul, M-N Marson, L Gérard and 4 more

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Immunoglobulin G subclasses confer protection againstProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. In Translation: FcRn across the Therapeutic Spectrum.International journal of molecular sciences · 2021
    Review
  16. VNTR2/VNTR3 genotype in theTherapeutic advances in neurological disorders · 2021
    Article
  17. The importance of FcRn in neuro-immunotherapies: From IgG catabolism,Therapeutic advances in neurological disorders · 2021
    Review
  18. Review
  19. The Pharmacogenetics of Rituximab: Potential Implications for Anti-CD20 Therapies in Multiple Sclerosis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 8 institutions in 3 countries.

V Gouilleux-GruartCNRS UMR 7292, Université François Rabelais, CHRU de Tours, Tours, France.
H Chapel
S Chevret
M Lucas
M Malphettes
C Fieschi
S Patel
D Boutboul
M-N Marson
L Gérard
M Lee
H Watier
E Oksenhendler
DEFI study group
University of Oxford · GBAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Tours · FRUniversité Paris Cité · FRCentre National de la Recherche Scientifique · FRDélégation Paris 7 · FRSorbonne Paris Cité · FRUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Biomarkers, PharmacologicalAdultCohort StudiesCommon Variable ImmunodeficiencyFemaleHistocompatibility Antigens Class IHumansImmunoglobulins, IntravenousInjections, SubcutaneousMaleMiddle AgedMinisatellite RepeatsPhenotypePolymorphism, GeneticPromoter Regions, GeneticProspective StudiesBiomarkers, PharmacologicalFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulins, IntravenousReceptors, Fc

Identifiers

PMID23286945
PMCPMC3573289
OpenAlexW2136123895

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.