Evidence map›Paper›PMID 38840663›Full record

ArticleResearch and practice in thrombosis and haemostasis2024

High levels of anti-factor VIII immunoglobulin G4 and immunoglobulin G total are associated with immune tolerance induction failure in people with congenital hemophilia A and high-responding inhibitors.

Daniel Gonçalves Chaves, Brendon Ayala da Silva Santos, Luciana Werneck Zucherato, Maíse Moreira Dias, Claudia Santos Lorenzato, Andrea Gonçalves de Oliveira, Mônica Hermida Cerqueira, Rosângela de Albuquerque Ribeiro, Leina Yukari Etto, Vivian Karla Brognoli Franco and 6 more

Abstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2024. 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

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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. Observational
  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

16 authors.

Daniel Gonçalves ChavesFundação Centro de Hematologia e Hemoterapia do Estado de Minas Gerais (HEMOMINAS), Belo Horizonte, Brazil.
Brendon Ayala da Silva SantosFaculty of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Luciana Werneck ZucheratoFaculty of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Maíse Moreira DiasFaculty of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Claudia Santos LorenzatoCentro de Hematologia e Hemoterapia do Paraná (HEMEPAR), Curitiba, Brazil.
Andrea Gonçalves de OliveiraFundação Centro de Hematologia e Hemoterapia do Estado de Minas Gerais (HEMOMINAS), Belo Horizonte, Brazil.
Mônica Hermida CerqueiraInstituto de Hematologia do Estado do Rio de Janeiro (HEMORIO), Rio de Janeiro, Brazil.
Rosângela de Albuquerque RibeiroCentro de Hematologia e Hemoterapia do Ceará (HEMOCE), Fortaleza, Brazil.
Leina Yukari EttoHemocentro da Paraíba (HEMOÍBA), João Pessoa, Brazil.
Vivian Karla Brognoli FrancoCentro de Hematologia e Hemoterapia de Santa Catarina (HEMOSC), Florianópolis, Brazil.
Maria do Rosário Ferraz RobertiHemocentro de Goiás (HEMOGO), Goiânia, Brazil.
Fábia Michelle Rodrigues de Araújo CalladoFundação de Hematologia e Hemoterapia de Pernambuco (HEMOPE), Recife, Brazil.
Maria Aline Ferreira de CerqueiraCentro de Hematologia e Hemoterapia do Piauí (HEMOPI), Teresina, Brazil.
Ieda PintoFundação Centro de Hemoterapia e Hematologia do Pará (HEMOPA), Belém, Brazil.
Ricardo Mesquita CameloFaculty of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Suely Meireles RezendeFaculty of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune tolerance induction (ITI) is the treatment of choice to eradicate neutralizing anti-factor (F)VIII alloantibodies (inhibitors) in people with inherited hemophilia A. However, it is not successful in 10% to 40% of the cases. The biological mechanisms and biomarkers associated with ITI outcome are largely unknown. Objectives: The aim of this study was to investigate the association of plasma cytokines (interferon-γ, tumor necrosis factor, interleukin [IL]-2, IL-4, IL-5, IL-6, IL-10, and IL-17A), chemokines (IL-8/CXCL8, RANTES/CCL5, MIG/CXCL9, MCP-1/CCL2, and IP-10/CXCL10), and anti-FVIII immunoglobulin (Ig) G total, IgG1, and IgG4 with ITI outcome. Methods: In this cross-sectional analysis of the Brazilian Immune Tolerance Study, we assessed plasma levels of anti-FVIII IgGs using an enzyme-linked immunosorbent assay with plasma-derived FVIII and recombinant FVIII as target antigens, immobilized in microplates. Results: We assayed 98 plasma samples of moderately severe and severe (FVIII activity, <2%) people with hemophilia A after completion of a first ITI course. Levels of anti-recombinant FVIII IgG total and IgG4 were higher in people with hemophilia A who failed ITI (IgG total optical density [OD], 0.37; IQR, 0.15-0.73; IgG4 OD, 2.19; IQR, 0.80-2.52) than in those who had partial (IgG total OD, 0.03; IQR, 0.00-0.14; IgG4 OD, 0.39; IQR, 0.09-1.11; Conclusion: Our results show that high levels of plasma anti-FVIII IgG4 and IgG total are associated with ITI failure.

Indexed as

alloantibodieschemokinecytokinefactor VIIIhemophilia Aimmune tolerance

Identifiers

PMID38840663
PMCPMC11152708

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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.