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Autoimmunity Reviews

Publication date: 2021-02-01
Volume: 20
Publisher: Elsevier

Author:

Bruner, Mads
Dige, Anders ; Loft, Anne Gitte ; Laurberg, Trine Bay ; Agnholt, Jorgen Steen ; Clemmensen, Kare ; McInnes, Iain ; Lories, Rik ; Iversen, Lars ; Hjuler, Kasper Fjellhaugen ; Kragstrup, Tue Wenzel

Keywords:

Science & Technology, Life Sciences & Biomedicine, Immunology, Autoimmunity, Immune mediated inflammatory disease, Spondyloarthritis, Psoriatic arthritis, Spondylitis, Psoriasis, Enthesitis, Enterocolitis, Dactylitis, Uveitis, Peripheral synovitis, Inflammatory bowel disease, Crohn's disease, Ulcerative colitis, Noninfectious uveitis, JANUS KINASE INHIBITOR, PROPRIA T-LYMPHOCYTES, DOUBLE-BLIND, PLAQUE PSORIASIS, CROHNS-DISEASE, ANKYLOSING-SPONDYLITIS, MONOCLONAL-ANTIBODY, PHASE-III, PLACEBO, EFFICACY, Arthritis, Psoriatic, Humans, Synovitis, 1107 Immunology, 3202 Clinical sciences, 3204 Immunology

Abstract:

Axial spondyloarthritis (axSpA), psoriatic arthritis (PsA), psoriasis, inflammatory bowel disease (IBD), and noninfectious uveitis form a distinct group among the immune mediated inflammatory diseases. Thus, many patients suffer from more than one of these disease manifestations. Here, we will use the term spondylitis-psoriasis-enthesitis-enterocolitis-dactylitis-uveitis-peripheral synovitis (SPEED-UP) spectrum disease. The aim is to review the new targeted pharmacological treatment options for all these diseases. All biological or targeted synthetic drugs with U.S. Food and Drug Administration (FDA) or European Medicines Agency (EMA) approval for any of the diagnoses axSpA, PsA, psoriasis, IBD, or non-infectious uveitis were included. Some of the drugs have documented efficacy in more than one of the diseases, e.g. tumor necrosis factor (TNF) inhibitors. However, other drugs are particularly effective for a specific inflamed tissue and approved in only one or two of the disease entities, e.g. abatacept for peripheral arthritis and vedolizumab for inflammatory bowel disease. This contributes with bedside to bench understanding of the immunology underlying this disease spectrum and provides clinicians with an overview that can assist stratified treatment decisions. We hope that this review will help guide clinicians to speed up treatment of patients with this disease spectrum.