Comprehensive exploratory autoantibody profiling in patients with early rheumatoid arthritis treated with methotrexate or tocilizumab

PLoS One. 2020 Dec 10;15(12):e0241189. doi: 10.1371/journal.pone.0241189. eCollection 2020.

Abstract

Background: We sought to identify immunoglobin G autoantibodies predictive of early treatment response to methotrexate, the recommended first-line therapy for patients with newly diagnosed rheumatoid arthritis, and to the interleukin-6 receptor inhibitor biologic tocilizumab, initiated as the first disease-modifying anti-rheumatic drug.

Materials and methods: In baseline sera of a subset of patients with newly diagnosed rheumatoid arthritis in the U-Act-Early study, selected based on specific responder/non-responder criteria using the Disease Activity Score assessing 28 joints (DAS28) within the first 20 weeks, we measured immunoglobin G antibody reactivity against 463 protein antigens and performed supervised cluster analysis to identify predictive autoantibodies for treatment response. The analysis subset comprised 56 patients in the methotrexate arm (22 responders, 34 non-responders) and 50 patients in the tocilizumab arm (34 responders, 16 non-responders). For comparison, these analyses were also performed in 50 age- and gender-matched healthy controls.

Results: Increased reactivity in responders versus non-responders was found in the methotrexate arm against two antigens-DOT1-like histone lysine methyltransferase (p = 0.009) and tropomyosin (p = 0.003)-and in the tocilizumab arm against one antigen-neuro-oncological ventral antigen 2 (p = 0.039). Decreased reactivity was detected against two antigens in the methotrexate arm-G1 to S phase transition 2 (p = 0.023) and the zinc finger protein ZPR1 (p = 0.021). Reactivity against the identified antigens was not statistically significant in either treatment arm for patients with rheumatoid factor-positive versus-negative or anti-cyclic citrullinated test-positive versus test-negative rheumatoid arthritis (p ≥ 0.06).

Conclusions: Comprehensive profiling of baseline sera revealed several novel immunoglobin G autoantibodies associated with early treatment response to methotrexate and to tocilizumab in disease-modifying anti-rheumatic drug-naive patients with rheumatoid arthritis. These findings could eventually yield clinically relevant predictive markers, if corroborated in different patient cohorts, and may facilitate future benefit in personalised healthcare.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • Antirheumatic Agents / therapeutic use*
  • Arthritis, Rheumatoid / drug therapy*
  • Arthritis, Rheumatoid / immunology*
  • Autoantibodies / blood*
  • Biomarkers / blood
  • Case-Control Studies
  • Double-Blind Method
  • Female
  • Histone-Lysine N-Methyltransferase / immunology
  • Humans
  • Immunoglobulin G / blood
  • Male
  • Membrane Transport Proteins / immunology
  • Methotrexate / therapeutic use*
  • Middle Aged
  • Nerve Tissue Proteins / immunology
  • Neuro-Oncological Ventral Antigen
  • Peptide Termination Factors / immunology
  • RNA-Binding Proteins / immunology
  • Tropomyosin / immunology

Substances

  • Antibodies, Monoclonal, Humanized
  • Antirheumatic Agents
  • Autoantibodies
  • Biomarkers
  • Immunoglobulin G
  • Membrane Transport Proteins
  • NOVA2 protein, human
  • Nerve Tissue Proteins
  • Neuro-Oncological Ventral Antigen
  • Peptide Termination Factors
  • RNA-Binding Proteins
  • TPM1 protein, human
  • Tropomyosin
  • ZPR1 protein, human
  • peptide-chain-release factor 3
  • DOT1L protein, human
  • Histone-Lysine N-Methyltransferase
  • tocilizumab
  • Methotrexate

Grants and funding

This autoantibody profiling analysis that used patient samples from the U-Act-Early study was jointly designed by investigators from the University Medical Center (Utrecht, Netherlands) and AP-S, JD, and MEAB, and was funded by Roche Nederland BV/F. Hoffmann-La Roche, CH. The funder provided support in the form of salaries for several authors who are full-time employees of Roche (JD, AP-S, MEAB), but, other than the roles of these authors, did not take any additional part in the study design, data collection and analysis, decision to publish or preparation of the manuscript. The specific roles of the authors are articulated in the ‘author contributions’ section.