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Semin Immunopathol. 2017 Jun;39(4):343-354. doi: 10.1007/s00281-017-0633-1. Epub 2017 May 15.

Cellular and molecular perspectives in rheumatoid arthritis.

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The Centre for Arthritis and Rheumatic Diseases, University College Dublin, Dublin 4, Ireland.
The Centre for Arthritis and Rheumatic Diseases, St. Vincent's University Hospital, Dublin 4, Ireland.
The Centre for Arthritis and Rheumatic Diseases, University College Dublin, Dublin 4, Ireland.
The Department of Molecular Rheumatology, Trinity College Dublin, Dublin 2, Ireland.


Synovial immunopathology in rheumatoid arthritis is complex involving both resident and infiltrating cells. The synovial tissue undergoes significant neovascularization, facilitating an influx of lymphocytes and monocytes that transform a typically acellular loose areolar membrane into an invasive tumour-like pannus. The microvasculature proliferates to form straight regularly-branching vessels; however, they are highly dysfunctional resulting in reduced oxygen supply and a hypoxic microenvironment. Autoantibodies such as rheumatoid factor and anti-citrullinated protein antibodies are found at an early stage, often before arthritis has developed, and they have been implicated in the pathogenesis of RA. Abnormal cellular metabolism and mitochondrial dysfunction thus ensue and, in turn, through the increased production of reactive oxygen species actively induce inflammation. Key pro-inflammatory cytokines, chemokines and growth factors and their signalling pathways, including nuclear factor κB, Janus kinase-signal transducer, are highly activated when immune cells are exposed to hypoxia in the inflamed rheumatoid joint show adaptive survival reactions by activating. This review attempts to highlight those aberrations in the innate and adaptive immune systems including the role of genetic and environmental factors, autoantibodies, cellular alterations, signalling pathways and metabolism that are implicated in the pathogenesis of RA and may therefore provide an opportunity for therapeutic intervention.


Angiogenesis; B-cells; Fibroblasts; Hypoxia; Rheumatoid arthritis; Synovial tissue; T-cells

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