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Review
From patients with arthralgia, pre-RA and recently diagnosed RA: what is the current status of understanding RA pathogenesis?
  1. Marlieke Molendijk,
  2. Johanna MW Hazes and
  3. Erik Lubberts
  1. Department of Rheumatology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands
  1. Correspondence to Dr Erik Lubberts; E.Lubberts{at}erasmusmc.nl

Abstract

It is believed that therapy for rheumatoid arthritis (RA) is the most effective and beneficial within a short time frame around RA diagnosis. This insight has caused a shift from research in patients with established RA to patients at risk of developing RA and recently diagnosed patients. It is important for improvement of RA therapy to understand when and what changes occur in patients developing RA. This is true for both seropositive and seronegative patients. Activation of the immune system as presented by autoantibodies, increased cytokine and chemokine production, and alterations within several immune cells occur during RA development. In this review we describe RA pathogenesis with a focus on knowledge obtained from patients with arthralgia, pre-RA and recently diagnosed RA. Connections are proposed between altered immune cells, cytokines and chemokines, and events like synovial hyperplasia, pain and bone damage.

  • early rheumatoid arthritis
  • cytokines
  • inflammation

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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Footnotes

  • Contributors MM performed the literature research, designed the layout and wrote the review. JMWH designed the layout, contributed to the clinical sections and revised the manuscript. EL designed the layout, contributed to immunological sections and revised the manuscript.

  • Funding This study was funded by the Dutch Arthritis Foundation (DAF 12-2-409) to EL.

  • Competing interests None declared.

  • Provenance and peer review Commissioned; externally peer reviewed.

  • Data sharing statement No additional data are available.