The Prevalence of Anti-Hexokinase-1 and Anti-Kelch-Like 12 Peptide Antibodies in Patients With Primary Biliary Cholangitis Is Similar in Europe and North America: A Large International, Multi-Center Study.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2019
Historique:
received: 17 12 2018
accepted: 11 03 2019
entrez: 20 4 2019
pubmed: 20 4 2019
medline: 10 7 2020
Statut: epublish

Résumé

Primary biliary cholangitis (PBC), formerly known as primary biliary cirrhosis, is present worldwide. Autoantibodies, in particular anti-mitochondrial antibodies (AMA) detected by indirect immunofluorescence assays or newer solid phase immunoassays can detect most, but not all individuals with PBC. Detection of antibodies to the anti-nuclear antigens sp100 and gp210 can identify additional PBC patients, but some seronegative patients remain, often resulting in delayed diagnosis and treatment. Antibodies to kelch-like 12 (KLHL12) and hexokinase 1 (HK-1) were recently identified as new biomarkers for PBC and notably identify patients who are negative for conventional autoantibodies. To become globally adopted, it is important to validate these new biomarkers in different geographic areas. In the present study we evaluated the prevalence of anti-KLHL12 (measured by a KLHL12-derived peptide referred to as KL-p) and anti-HK-1 antibodies by ELISA at five sites within Europe and North America and demonstrated the presence of these antibodies in patients with PBC in all geographies.

Identifiants

pubmed: 31001269
doi: 10.3389/fimmu.2019.00662
pmc: PMC6456688
doi:

Substances chimiques

Adaptor Proteins, Signal Transducing 0
Autoantibodies 0
Biomarkers 0
KLHL12 protein, human 0
Peptides 0
HK1 protein, human EC 2.7.1.1
Hexokinase EC 2.7.1.1

Types de publication

Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

662

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Auteurs

Gary L Norman (GL)

Department of Research and Development, Inova Diagnostics, San Diego, CA, United States.

Anna Reig (A)

Liver Unit, Hospital Clínic, Institut D'Investigacions Biomèdiques August Pi i Sunyer, CIBERehd, University of Barcelona, Barcelona, Spain.

Odette Viñas (O)

Immunology Department, Hospital Clínic, Centre Diagnòstic Biomèdic, Institut D'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.

Michael Mahler (M)

Department of Research and Development, Inova Diagnostics, San Diego, CA, United States.

Ewa Wunsch (E)

Translational Medicine Group, Pomeranian Medicine University, Szczecin, Poland.

Piotr Milkiewicz (P)

Translational Medicine Group, Pomeranian Medicine University, Szczecin, Poland.
Liver and Internal Medicine Unit, Department General, Transplant and Liver Surgery, Medical University of Warsaw, Warsaw, Poland.

Mark G Swain (MG)

Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.

Andrew Mason (A)

Division of Gastroenterology (Liver Unit), University of Alberta, Edmonton, AB, Canada.

Laura M Stinton (LM)

Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.

Maria Belen Aparicio (MB)

Laboratorio Autoimmunidad, Hospital Universitario de Salamanca, Salamanca, Spain.

Maria Jose Aldegunde (MJ)

Laboratorio Autoimmunidad, Hospital Universitario de Salamanca, Salamanca, Spain.

Marvin J Fritzler (MJ)

Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.

Albert Parés (A)

Liver Unit, Hospital Clínic, Institut D'Investigacions Biomèdiques August Pi i Sunyer, CIBERehd, University of Barcelona, Barcelona, Spain.

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Classifications MeSH