Literature DB >> 32896247

Mass-spectrometric identification of carbamylated proteins present in the joints of rheumatoid arthritis patients and controls.

Marije K Verheul1, George M C Janssen2, Arnoud de Ru2, Gerrie Stoeken-Rijsbergen3, E W Nivine Levarht3, Joanneke C Kwekkeboom3, Nils Bomer4, Andreea Ioan-Facsinay3, Ingrid Meulenbelt4, Robert A Cordfunke5, Jan W Drijfhout5, Rene E M Toes3, Peter A van Veelen2, Leendert A Trouw6.   

Abstract

OBJECTIVES: Antibodies targeting post-translationally modified proteins, such as anti-carbamylated protein antibodies (anti-CarP antibodies) are present in the sera of rheumatoid arthritis (RA) patients. These autoantibodies associate with increased risk of RA development and with severity of joint destruction. It is not known which proteins in the RA joint are recognised by anti-CarP antibodies. Therefore, we investigated the presence and identity of carbamylated proteins in the human (inflamed) joint.
METHODS: We obtained synovium, cartilage and synovial fluid from RA joints. Cartilage and synovium were obtained from controls. Samples were processed and used for immunohistochemistry or mass-spectrometric analysis to investigate the presence of carbamylated proteins. Anti-CarP antibody reactivity towards identified carbamylated proteins was tested by ELISA.
RESULTS: Immunohistochemistry showed extensive staining of RA and control synovial tissue. Whole proteome analyses of the joint tissues revealed a large number of carbamylated peptidyllysine residues. We identified many carbamylated proteins in cartilage and were also able to detect carbamylation in synovial tissue and synovial fluid. Carbamylation was not exclusive to the RA joint and was also present in the joints of controls. Anti-CarP antibodies in the sera of RA patients were able to recognise the identified carbamylated proteins.
CONCLUSIONS: We conclude that numerous carbamylated proteins are present in the RA joint. These carbamylated proteins can be recognised by anti-CarP antibodies, substantiating the notion that anti-CarP antibodies may play a role in the pathogenesis of RA.

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Year:  2020        PMID: 32896247

Source DB:  PubMed          Journal:  Clin Exp Rheumatol        ISSN: 0392-856X            Impact factor:   4.473


  5 in total

Review 1.  Redox-Mediated Carbamylation As a Hapten Model Applied to the Origin of Antibodies to Modified Proteins in Rheumatoid Arthritis.

Authors:  Maria Isabel Trejo-Zambrano; Eduardo Gómez-Bañuelos; Felipe Andrade
Journal:  Antioxid Redox Signal       Date:  2021-06-04       Impact factor: 7.468

2.  Human carbamylome description identifies carbamylated α2-macroglobulin and hemopexin as two novel autoantigens in early rheumatoid arthritis.

Authors:  Paschalis Sidiras; Jessica Lechanteur; Virginie Imbault; Tatiana Sokolova; Patrick Durez; Valérie Gangji; David Communi; Joanne Rasschaert
Journal:  Rheumatology (Oxford)       Date:  2022-07-06       Impact factor: 7.046

3.  Autoantibodies against specific post-translationally modified proteins are present in patients with lupus and associate with major neuropsychiatric manifestations.

Authors:  Rory C Monahan; Michelle D van den Beukel; Nicole V Borggreven; Rolf Fronczek; Tom W J Huizinga; Margreet Kloppenburg; Gerda M Steup-Beekman; Leendert A Trouw
Journal:  RMD Open       Date:  2022-04

4.  The value of anti-CarP and anti-PAD4 as markers of rheumatoid arthritis in ACPA/RF negative rheumatoid arthritis patients.

Authors:  Bogdan Kolarz; Marek Ciesla; Ann K Rosenthal; Magdalena Dryglewska; Maria Majdan
Journal:  Ther Adv Musculoskelet Dis       Date:  2021-02-11       Impact factor: 5.346

5.  Anti-Carbamylated Fibrinogen Antibodies Might Be Associated With a Specific Rheumatoid Phenotype and Include a Subset Recognizing In Vivo Epitopes of Its γ Chain One of Which Is Not Cross Reactive With Anti-Citrullinated Protein Antibodies.

Authors:  Pauline Brevet; Claire Lattard; Clément Guillou; Pascal Rottenberg; Patrice Fardellone; Xavier Le-Loët; Thierry Lequerré; Pascal Cosette; Olivier Boyer; Manuel Fréret; Olivier Vittecoq
Journal:  Front Immunol       Date:  2021-10-07       Impact factor: 7.561

  5 in total

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