4.7 Review

Insights Into Leukocyte Trafficking in Inflammatory Arthritis - Imaging the Joint

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出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2021.635102

关键词

imaging; leukocyte; adhesion; migration; arthritis

资金

  1. MRC iCase [MR/P016154/1]
  2. MRC-Versus Arthritis Centre for Musculoskeletal Ageing Research Ph.D. studentship [MR/R502364/1]
  3. Kennedy Trust for Rheumatology Research
  4. MRC [MR/T028025/1]
  5. MRC [MR/T028025/1] Funding Source: UKRI

向作者/读者索取更多资源

The inappropriate accumulation and activation of leukocytes is a common feature in immune-mediated inflammatory diseases, and efforts to modulate leukocyte entry and exit from joints have been unsuccessful. Technological advancements have allowed for real-time tracking of leukocyte movement in arthritic joints, increasing our understanding of the mechanisms underlying pathological leukocyte accumulation. This review explores the mechanisms of inappropriate leukocyte trafficking in inflammatory arthritis and highlights advances in joint imaging and ex vivo joint constructs.
The inappropriate accumulation and activation of leukocytes is a shared pathological feature of immune-mediated inflammatory diseases (IMIDs), such as rheumatoid arthritis (RA) and psoriatic arthritis (PsA). Cellular accumulation is therefore an attractive target for therapeutic intervention. However, attempts to modulate leukocyte entry and exit from the joint have proven unsuccessful to date, indicating that gaps in our knowledge remain. Technological advancements are now allowing real-time tracking of leukocyte movement through arthritic joints or in vitro joint constructs. Coupling this technology with improvements in analyzing the cellular composition, location and interactions of leukocytes with neighboring cells has increased our understanding of the temporal dynamics and molecular mechanisms underpinning pathological accumulation of leukocytes in arthritic joints. In this review, we explore our current understanding of the mechanisms leading to inappropriate leukocyte trafficking in inflammatory arthritis, and how these evolve with disease progression. Moreover, we highlight the advances in imaging of human and murine joints, along with multi-cellular ex vivo joint constructs that have led to our current knowledge base.

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