Evidence map›Paper›PMID 41315117›Full record

ArticleJournal of clinical immunology2025

IgA and IgM-enriched Immunoglobulins in Primary Immunodeficiencies: a Pilot Study.

Aurore Collet, Benjamin Coiffard, Emmanuel Ledoult, Claire Fieschi, Morgane Cheminant, Alexandra Serris, Felipe Suarez, Sébastien Sanges, Antoine Neel, Raphaële Nove-Josserand and 28 more

Abstract read
In one paragraph

Article in Journal of clinical immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

38 authors.

Aurore ColletUniv. Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, F-59000, France. aurore.collet@chu-lille.fr.ORCID http://orcid.org/0000-0002-8279-1912
Benjamin CoiffardDepartment of Respiratory Medicine and Lung Transplantation, APHM, Hôpital Nord, Aix- Marseille University, Marseille, France.
Emmanuel LedoultUniv. Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, F-59000, France.
Claire FieschiService d'Immunologie Clinique, Saint Louis Hôpital, AP-HP, Université de Paris Cité, Paris, France.
Morgane CheminantDepartment of Hematology, Necker - Enfants Malades Hospital, Assistance Publique des Hopitaux de Paris (APHP), Université Paris Cité, Institut IMAGINE INSERM U1163, Paris, France.
Alexandra SerrisService de Maladies Infectieuses et Tropicales, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux Paris, Paris, France.
Felipe SuarezDepartment of Hematology, Necker - Enfants Malades Hospital, Assistance Publique des Hopitaux de Paris (APHP), Université Paris Cité, Institut IMAGINE INSERM U1163, Paris, France.
Sébastien SangesUniv. Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, F-59000, France.
Antoine NeelInternal Medicine Department, Hotel Dieu, Nantes University Hospital, Nantes, France.
Raphaële Nove-JosserandCentre de ressources et de compétences pour la mucoviscidose adulte, Service de médecine interne et vasculaire, Hospices Civils de Lyon, Lyon, France.
Sarah StablerUniv. Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, F-59000, France.
Kinan El HusseiniINSERM, Centre de recherche sur l'inflammation, Service de Pneumologie et Transplantation Pulmonaire, AP-HP, Hôpital Bichat, Université Paris Cité, Paris, France.
Alice HuaultPediatric Department, Saint Nazaire General Hospital, St-Nazaire, France.
Pierre CougoulDepartment of Internal Medicine, Toulouse University Cancer Institute (IUCT) Oncopole, Toulouse, France.
Christelle MausserveyInternal Medicine Department, Centre Hospitalier William-Morey, Chalon/Saône, France.
Nadim CassirInfectious Diseases, Aix-Marseille University, IRD, AP-HM, Mephi,, Marseille, France.
Floriane MirgotInstitute of Immunology, CHU Lille, Lille, F-59000, France.
Bertrand MeresseUniv. Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, F-59000, France.
Arnaud DendoovenUniv. Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, F-59000, France.
Sandrine PoizotInstitute of Immunology, CHU Lille, Lille, F-59000, France.
Tanguy Le ScornetInternal Medicine Department, Hotel Dieu, Nantes University Hospital, Nantes, France.
Anne-Sophie BravardCH Avranches, Avranches, France.
Anne ConradService des maladies infectieuses et tropicales, Hôpital de la Croix- Rousse, Hospices Civils de Lyon, Lyon, France.
Manon LevêqueDepartment of Respiratory Medicine and Lung Transplantation, APHM, Hôpital Nord, Aix- Marseille University, Marseille, France.
Jehane FadlallahService d'Immunologie Clinique, Saint Louis Hôpital, AP-HP, Université de Paris Cité, Paris, France.
Cléa MelenotteService de Maladies Infectieuses et Tropicales, Hôpital Necker Enfants Malades, Assistance Publique Hôpitaux Paris, Paris, France.
Chloë Dumas De La RoqueService de Médecine Interne, Hôpital Haut-L'évêque, Bordeaux, France.
Claire TinevezService de Médecine Interne, Hôpital Haut-L'évêque, Bordeaux, France.
Wadih Abou ChahlaCEREDIH Lille, Regional Center for Primary Immune Deficiency, CHU Lille, Lille, F-59000, France.
Sylvain DubucquoiUniv. Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, F-59000, France.
Myriam LabaletteUniv. Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, F-59000, France.
Bénédicte NevenPediatric Immunology-Hematology and Rheumatology Unit, Necker- Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP) Centre, Paris, France.
Marion MalphettesService d'Immunologie Clinique, Saint Louis Hôpital, AP-HP, Université de Paris Cité, Paris, France.
Nicolas SchleinitzDépartement de Médecine Interne, Timone Hospital, Assistance Publique-Hôpitaux de Marseille, Aix-Marseille Université, Marseille, France.
Lionel GalicierDépartement de Médecine Interne, Timone Hospital, Assistance Publique-Hôpitaux de Marseille, Aix-Marseille Université, Marseille, France.
Jean-François ViallardService de Médecine Interne, Hôpital Haut-L'évêque, Bordeaux, France.
Guy GorochovSorbonne Université, Inserm, Centre d'Immunologie et des Maladies Infectieuses, AP-HP, Hôpital de la Pitié-Salpêtrière, Paris, France.
Guillaume LefèvreUniv. Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, F-59000, France.

Funding

European Union's HORIZON-HLTH-2021- DISEASE-04 program Grant agreement No. 101057100 (UNDINE)French Foundation for Medical Research (FRM) Paris FRM EQU202203014622French National Research Agency ANR-RHU COVIFERON Program ANR-21-RHUS-08
6 · The paper itself

Abstract

purposeDespite well-conducted replacement therapy with polyvalent immunoglobulins (IgRT), some patients with primary immunodeficiencies (PID) continue to experience recurrent or chronic infections. IgA and IgM, essential for mucosal and complement-mediated immunity, are absent or minimal in standard immunoglobulin products. The aim of this study is to evaluate the safety and clinical evolution profiles in PID patients with undetectable IgA/IgM levels and persistent infections despite standard IgRT, after introduction of an IgA- and IgM-enriched immunoglobulin preparation (IgGAM, Pentaglobin

methodsA compassionate use program (CUP) in France enrolled 20 PID patients with undetectable IgA/IgM levels, receiving IgGAM IV infusions every 7-14 days. Tolerance, infection frequency, hospitalizations, and biological markers (Ig levels, complement activation, salivary IgA) were analyzed prospectively.

resultsTwenty patients were included in the CUP at the time of analysis. No severe adverse event was reported. Half of the patients experienced mild to moderate hypersensitivity symptoms. Mean antibiotic courses dropped from 5.4 to 2.3/year (p = 0.0009) and mean number of hospitalizations decreased from 2.6 to 1.2/year (p = 0.01). Median serum IgA and IgM levels increased three months after IgGAM start. IgM and low levels of IgA were detected in saliva samples, suggesting at least a transient transfer of IgA/IgM from IgGAM into mucosal fluids.

conclusionIn patients with severe PID and undetectable IgA/IgM, IgGAM was associated with reduced infections and hospitalizations. Controlled studies are needed to confirm the benefit of IgA/M enriched immunoglobulin preparations in PID patients with persistent and/or recurrent respiratory or digestive infections.

Indexed as

Immunoglobulin AImmunoglobulin MImmunoglobulins, IntravenousImmunologic Deficiency SyndromesPrimary Immunodeficiency DiseasesAdolescentAdultChildChild, PreschoolFemaleHumansMaleMiddle AgedPilot ProjectsTreatment OutcomeYoung AdultImmunoglobulin AImmunoglobulin MImmunoglobulins, IntravenousIgA and IgM-enriched immunoglobulinImmunoglobulin AImmunoglobulin MInborn errors of immunityPolyvalent immunoglobulinsPrimary immunodeficiency

Identifiers

PMID41315117
PMCPMC12783217

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.