PAD4 Immunization Triggers Anti-Citrullinated Peptide Antibodies in Normal Mice: Analysis With Peptide Arrays.


Journal

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

Informations de publication

Date de publication:
2022
Historique:
received: 20 12 2021
accepted: 04 03 2022
entrez: 18 4 2022
pubmed: 19 4 2022
medline: 20 4 2022
Statut: epublish

Résumé

The critical immunological event in rheumatoid arthritis (RA) is the production of antibodies to citrullinated proteins (ACPAs), ie proteins on which arginines have been transformed into citrullines by peptidyl arginine deiminases (PAD). In C3H mice, immunization with PAD4 triggers the production of ACPAs. Here, we developed a peptide array to analyze the fine specificity of anti-citrullinated peptide antibodies and used it to characterize the ACPA response after hPAD4 immunization in mice expressing different H-2 haplotypes. Sera from C3H, DBA/2, BALB/c and C57BL/6 mice immunized with human PAD4 (hPAD4) or control-matched mice immunized with phosphate buffered saline (PBS) were used to screen peptide arrays containing 169 peptides from collagen, filaggrin, EBNA, proteoglycan, enolase, alpha and beta fibrinogen, histon and vimentin. Human PAD4 immunization induced antibodies directed against numerous citrullinated peptides from fibrinogen, histon 4 and vimentin. Most peptides were recognized under their arginine and citrullinated forms. DBA/2 and BALB/c mice (H-2d) had the lowest anti-citrullinated peptide IgG responses. C3H (H-2k) and BL6 mice (H-2b) had the highest anti-citrullinated peptide IgG responses. The newly developed peptide array allows us to characterize the ACPA production after hPAD4 immunization in mice on the H-2d, H-2k or H-2b backgrounds. This sensitive tool will be useful for further studies on mice for prevention of ACPA production by PAD tolerization.

Identifiants

pubmed: 35432329
doi: 10.3389/fimmu.2022.840035
pmc: PMC9008206
doi:

Substances chimiques

Anti-Citrullinated Protein Antibodies 0
Autoantibodies 0
Immunoglobulin G 0
Peptides 0
Vimentin 0
Fibrinogen 9001-32-5
Arginine 94ZLA3W45F
Protein-Arginine Deiminase Type 4 EC 3.5.3.15
peptidylarginine deiminase 4, mouse EC 3.5.3.15

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

840035

Informations de copyright

Copyright © 2022 Hemon, Lambert, Arnoux, Roudier and Auger.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Marie F Hemon (MF)

Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche (UMRs) 1097, Aix Marseille University, Marseille, France.
Arthritis R&D, Neuilly-sur-Seine, France.

Nathalie C Lambert (NC)

Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche (UMRs) 1097, Aix Marseille University, Marseille, France.

Fanny Arnoux (F)

Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche (UMRs) 1097, Aix Marseille University, Marseille, France.

Jean Roudier (J)

Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche (UMRs) 1097, Aix Marseille University, Marseille, France.
Assistance Publique Hôpitaux de Marseille (APHM), Rhumatologie, Marseille, France.

Isabelle Auger (I)

Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche (UMRs) 1097, Aix Marseille University, Marseille, France.

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Classifications MeSH