Innate Immunity and Sex: Distinct Inflammatory Profiles Associated with Murine Pain in Acute Synovitis

• Published in: Cells (Basel, Switzerland) Vol. 12; no. 14; p. 1913
• Main Authors: Valdrighi, Natália, Blom, Arjen B, Vago, Juliana P, van Beuningen, Henk M, Vitters, Elly L, Helsen, Monique M, Walgreen, Birgitte, Arntz, Onno J, Koenders, Marije I, van der Kraan, Peter M, Blaney Davidson, Esmeralda N, van de Loo, Fons A J
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.07.2023; MDPI
• Subjects: Animals; Arthralgia; Arthritis; Cell walls; Cytokines; Demographic aspects; Experiments; Female; Gait; Gene expression; Humans; Immune response; Immune system; Immunity; Immunity, Innate; Inflammation; Inflammation - complications; inflammatory disease; Innate immunity; Joint diseases; Knee; Laboratories; Male; Males; Medical research; Medicine, Experimental; Mice; Neutrophils; Pain; Pain perception; Sex; sex differences; Sexes; Synovitis; Synovitis - metabolism; Netherlands; inflammatory disease; pain; arthritis; innate immunity; sex differences; synovitis
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells12141913

Joint pain severity in arthritic diseases differs between sexes and is often more pronounced in women. This disparity is thought to stem from biological mechanisms, particularly innate immunity, yet the understanding of sex-specific differences in arthritic pain remains incomplete. This study aims to investigate these disparities using an innate immunity-driven inflammation model induced by intra-articular injections of Streptococcus Cell Wall fragments to mimic both acute and pre-sensitized joint conditions. Nociceptive behavior was evaluated via gait analysis and static weight-bearing, and inflammation was evaluated via joint histology and the synovial gene expression involved in immune response. Although acute inflammation and pain severity were comparable between sexes, distinct associations between synovial inflammatory gene expression and static nociceptive behavior emerged. These associations delineated sex-specific relationships with pain, highlighting differential gene interactions ( versus on day 1 and versus on day 8) between sexes. In conclusion, our study found that, despite similar pain severity between sexes, the association of inflammatory synovial genes revealed sex-specific differences in the molecular inflammatory mechanisms underlying pain. These findings suggest a path towards more personalized treatment strategies for pain management in arthritis and other inflammatory joint diseases.