OBJECTIVE: Although osteoarthritis (OA) is considered a non-inflammatory condition, it is widely accepted that synovial inflammation is a feature of OA. However, the role of immune cells and their cytokines in OA is largely unknown. This narrative systematic review summarizes the knowledge of inflammatory properties, immune cells and their cytokines in synovial tissues (STs) of OA patients. DESIGN: Broad literature search in different databases was performed which resulted in 100 articles. RESULTS: Of 100 articles 33 solely investigated inflammation in OA ST with or without comparison with normal samples; the remaining primarily focussed on rheumatoid arthritis (RA) ST. Studies investigating different severity stages or cellular source of cytokines were sparse. OA ST displayed mild/moderate grade inflammation when investigated by means of haematoxylin and eosin (H&E) staining. Most frequently found cells types were macrophages, T cells and mast cells (MCs). Overall the number of cells was lower than in RA, although the number of MCs was as high as or sometimes even higher than in RA ST. Cytokines related to T cell or macrophage function were found in OA ST. Their expression was overall higher than in normal ST, but lower than in RA ST. Their cellular source remains largely unknown in OA ST. CONCLUSION: Inflammation is common in OA ST and characterized by immune cell infiltration and cytokine secretion. This inflammation seems quantitatively and qualitatively different from inflammation in RA. Further research is needed to clarify the role of inflammation, immune cells and their cytokines in the pathogenesis of OA.
OBJECTIVE: Although osteoarthritis (OA) is considered a non-inflammatory condition, it is widely accepted that synovial inflammation is a feature of OA. However, the role of immune cells and their cytokines in OA is largely unknown. This narrative systematic review summarizes the knowledge of inflammatory properties, immune cells and their cytokines in synovial tissues (STs) of OA patients. DESIGN: Broad literature search in different databases was performed which resulted in 100 articles. RESULTS: Of 100 articles 33 solely investigated inflammation in OA ST with or without comparison with normal samples; the remaining primarily focussed on rheumatoid arthritis (RA) ST. Studies investigating different severity stages or cellular source of cytokines were sparse. OA ST displayed mild/moderate grade inflammation when investigated by means of haematoxylin and eosin (H&E) staining. Most frequently found cells types were macrophages, T cells and mast cells (MCs). Overall the number of cells was lower than in RA, although the number of MCs was as high as or sometimes even higher than in RA ST. Cytokines related to T cell or macrophage function were found in OA ST. Their expression was overall higher than in normal ST, but lower than in RA ST. Their cellular source remains largely unknown in OA ST. CONCLUSION:Inflammation is common in OA ST and characterized by immune cell infiltration and cytokine secretion. This inflammation seems quantitatively and qualitatively different from inflammation in RA. Further research is needed to clarify the role of inflammation, immune cells and their cytokines in the pathogenesis of OA.
Authors: Hannah Labinsky; Paul M Panipinto; Kaytlyn A Ly; Deric K Khuat; Bhanupriya Madarampalli; Vineet Mahajan; Jonathan Clabeaux; Kevin MacDonald; Peter J Verdin; Jane H Buckner; Erika H Noss Journal: Arthritis Rheumatol Date: 2020-03-12 Impact factor: 10.995
Authors: Satyavrata Samavedi; Patricia Diaz-Rodriguez; Joshua D Erndt-Marino; Mariah S Hahn Journal: Tissue Eng Part A Date: 2016-11-18 Impact factor: 3.845
Authors: William J Pinamont; Natalie K Yoshioka; Gregory M Young; Vengadeshprabhu Karuppagounder; Elijah L Carlson; Adeel Ahmad; Reyad Elbarbary; Fadia Kamal Journal: J Vis Exp Date: 2020-05-06 Impact factor: 1.355
Authors: I Atukorala; C K Kwoh; A Guermazi; F W Roemer; R M Boudreau; M J Hannon; D J Hunter Journal: Ann Rheum Dis Date: 2014-12-08 Impact factor: 19.103