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Association between levels of synovial anti‐citrullinated peptide antibodies and neutrophil response in patients with rheumatoid arthritis
Authors:Carolina V. Gorlino  Mabel N. Dave  Rodrigo Blas  María I. Crespo  Alicia Lavanchy  Héctor Tamashiro  Rodolfo Pardo‐Hildalgo  María C. Pistoresi‐Palencia  María S. Di Genaro
Affiliation:1. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Instituto Multidisciplinario de Investigaciones Biológicas (IMIBIO‐SL), San Luis, Argentina;2. Universidad Nacional de San Luis, Facultad de Química, Bioquímica y Farmacia, San Luis, Argentina;3. Centro Médico MEDICI, San Luis, Argentina;4. Universidad Nacional de Córdoba, Facultad de Ciencias Químicas, Departamento de Bioquímica Clínica, Córdoba, Argentina;5. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Centro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)‐Córdoba, Argentina;6. Centro Médico CENYR, San Luis, Argentina;7. Clínica Bolívar, San Luis, Argentina;8. Centro de Rehabilitación Médica CER, San Juan, Argentina
Abstract:Rheumatoid arthritis (RA) is characterized by the presence of anti‐citrullinated peptide antibodies (ACPAs) and neutrophils infiltrating the synovial fluid (SF) of the affected joints. The aim of this work was to analyze whether the presence of ACPAs in SF is associated with neutrophil infiltration and with their phenotype in the inflamed joints of RA patients. We found that in the presence of ACPAs, the number of synovial neutrophils correlated with severe disease activity. The SF were divided according to synovial ACPA levels in negative‐ (<25 U/mL), low‐ (25–200 U/mL) and high level (?200 U/mL; ACPAhigh). We observed that IL‐6, IL‐17, and IL‐8 were significantly elevated in ACPAhighSF and that IL‐8 levels correlated positively with neutrophil counts and with worse clinical manifestations. Additionally, in vitro incubation of neutrophils with ACPAhigh SF resulted in an increased ROS production and extracellular DNA release compared to neutrophils incubated with ACPA‐negative SF. These exacerbated effector functions were associated with a fraction of ICAM‐1‐positive neutrophils, which were induced by ACPAhigh SF. Likewise, in in vivo, we could also detect this subset among neutrophils present in ACPAhigh SF. In conclusion, the data presented here shed light on the role of SF‐ACPAs as inductors of a proinflammatory profile in neutrophils.
Keywords:Anti‐citrullinated peptide autoantibodies  ICAM‐1  IL‐8  Neutrophils  Rheumatoid arthritis
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