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Disordered Antigens and Epitope Overlap Between Anti-Citrullinated Protein Antibodies and Rheumatoid Factor in Rheumatoid Arthritis.
Zheng, Zihao; Mergaert, Aisha M; Fahmy, Lauren M; Bawadekar, Mandar; Holmes, Caitlyn L; Ong, Irene M; Bridges, Alan J; Newton, Michael A; Shelef, Miriam A.
Affiliation
  • Zheng Z; University of Wisconsin-Madison.
  • Mergaert AM; University of Wisconsin-Madison.
  • Fahmy LM; University of Wisconsin-Madison.
  • Bawadekar M; University of Wisconsin-Madison.
  • Holmes CL; University of Wisconsin-Madison.
  • Ong IM; University of Wisconsin-Madison and University of Wisconsin Carbone Comprehensive Cancer Center.
  • Bridges AJ; University of Wisconsin-Madison and William S. Middleton Memorial Veterans Hospital.
  • Newton MA; University of Wisconsin-Madison.
  • Shelef MA; University of Wisconsin-Madison and William S. Middleton Memorial Veterans Hospital.
Arthritis Rheumatol ; 72(2): 262-272, 2020 02.
Article in En | MEDLINE | ID: mdl-31397047
ABSTRACT

OBJECTIVE:

Anti-citrullinated protein antibodies (ACPAs) and rheumatoid factor (RF) are commonly present in rheumatoid arthritis (RA) without a clear rationale for their coexistence. Moreover, autoantibodies develop against proteins with different posttranslational modifications and native proteins without obvious unifying characteristics of the antigens. We undertook this study to broadly evaluate autoantibody binding in seronegative and seropositive RA to identify novel features of reactivity.

METHODS:

An array was created using a total of 172,828 native peptides, citrulline-containing peptides, and homocitrulline-containing peptides derived primarily from proteins citrullinated in the rheumatoid joint. IgG and IgM binding to peptides were compared between cyclic citrullinated peptide (CCP)-positive RF+, CCP+RF-, CCP-RF+, and CCP-RF- serum from RA patients (n = 48) and controls (n = 12). IgG-bound and endogenously citrullinated peptides were analyzed for amino acid patterns and predictors of intrinsic disorder, i.e., unstable 3-dimensional structure. Binding to IgG-derived peptides was specifically evaluated. Enzyme-linked immunosorbent assay confirmed key results.

RESULTS:

Broadly, CCP+RF+ patients had high citrulline-specific IgG binding to array peptides and CCP+RF- and CCP-RF+ patients had modest citrulline-specific IgG binding (median Z scores 3.02, 1.42, and 0.75, respectively; P < 0.0001). All RA groups had low homocitrulline-specific binding. CCP+RF+ patients had moderate IgG binding to native peptides (median Z score 2.38; P < 0.0001). The highest IgG binding was to citrulline-containing peptides, irrespective of protein identity, especially if citrulline was adjacent to glycine or serine, motifs also seen in endogenous citrullination in the rheumatoid joint. Highly bound peptides had multiple features predictive of disorder. IgG from CCP+RF+ patients targeted citrulline-containing IgG-derived peptides.

CONCLUSION:

Disordered antigens, which are frequently citrullinated, and common epitopes for ACPAs and RF are potentially unifying features for RA autoantibodies.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arthritis, Rheumatoid / Rheumatoid Factor / Autoantigens / Anti-Citrullinated Protein Antibodies / Epitopes Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Arthritis Rheumatol Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arthritis, Rheumatoid / Rheumatoid Factor / Autoantigens / Anti-Citrullinated Protein Antibodies / Epitopes Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Arthritis Rheumatol Year: 2020 Document type: Article