Objective: Monocytes contribute to synovitis and disease pathogenesis in osteoarthritis (OA). Low-grade inflammation occurs in OA and correlates with disease severity and progression. Since monocyte development and function is altered by systemic inflammation, we analyzed monocyte numbers and function between individuals with knee OA and healthy age-and sex-matched controls. Design: We analyzed markers of soluble and cellular inflammation in peripheral blood of women with knee OA and compared them to healthy age-and sex-matched controls. Soluble inflammatory mediators (TNF, IL-6, IL-10 and CRP) in the serum were measured by high-sensitivity ELISA. Leukocyte numbers, surface expression of monocyte activation markers, and monocyte production of pro-inflammatory mediators (TNF and IL-1 beta) following stimulation were measured by flow cytometry. Results: Women with knee OA (n = 15) had elevated levels of serum c-reactive protein (CRP) and a lower proportion of circulating monocytes. Monocytes from OA participants had elevated expression of the activation markers CD16, CCR2, and HLA-DR and induced greater production of tumor necrosis factor (TNF) and IL-1 beta compared to healthy controls. Higher serum TNF and BMI were correlated with increased monocyte expression of CCR2. Additionally monocyte CCR2 expression and serum TNF were correlated with worse pain on a validated questionnaire. Conclusions: Our findings suggest monocytes are activated prior to their entry into the synovium. Modulating systemic inflammation and monocyte recruitment to the synovium could be of therapeutic benefit. (C) 2017 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
机构:
Baylor Coll Med, Michael E DeBakey VA Med Ctr, Houston, TX 77030 USABaylor Coll Med, Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
Lo, Grace H.
McAlindon, Timothy E.
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Tufts Med Ctr, Boston, MA USABaylor Coll Med, Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
McAlindon, Timothy E.
Katz, Jeffrey N.
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Brigham & Womens Hosp, Boston, MA 02115 USABaylor Coll Med, Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
Katz, Jeffrey N.
Driban, Jeffrey B.
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Tufts Med Ctr, Boston, MA USABaylor Coll Med, Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
Driban, Jeffrey B.
Price, Lori Lyn
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Tufts Univ, Boston, MA 02111 USABaylor Coll Med, Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
Price, Lori Lyn
Eaton, Charles
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Brown Univ, Providence, RI 02912 USABaylor Coll Med, Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
Eaton, Charles
Petersen, Nancy
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Hlth Serv Res & Dev Ctr Excellence, Michael E DeBakey VA Med Ctr, Houston, TX USABaylor Coll Med, Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
Petersen, Nancy
Ballantyne, Christie
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Baylor Coll Med, Houston, TX 77030 USABaylor Coll Med, Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
Ballantyne, Christie
Suarez-Almazor, Maria E.
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Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USABaylor Coll Med, Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
机构:
UIowa, Iowa City, IA USABoston Univ, Sch Med, Clin Epidemiol Res & Training Unit, Boston, MA 02118 USA
Frey-Law, Laura
Misra, Devyani
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Boston Univ, Sch Med, Clin Epidemiol Res & Training Unit, Boston, MA 02118 USABoston Univ, Sch Med, Clin Epidemiol Res & Training Unit, Boston, MA 02118 USA
Misra, Devyani
Nevitt, Michael C.
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UCSF, Epidemiol & Biostat, San Francisco, CA USABoston Univ, Sch Med, Clin Epidemiol Res & Training Unit, Boston, MA 02118 USA
Nevitt, Michael C.
Arendt-Nielsen, Lars
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Aalborg Univ, Aalborg, DenmarkBoston Univ, Sch Med, Clin Epidemiol Res & Training Unit, Boston, MA 02118 USA
Arendt-Nielsen, Lars
Quinn, Emily K.
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Boston Univ, Sch Publ Hlth, Data Coordinating Ctr, Boston, MA USABoston Univ, Sch Med, Clin Epidemiol Res & Training Unit, Boston, MA 02118 USA
Quinn, Emily K.
Lewis, Cora E.
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Univ Alabama Birmingham, Prevent Med, Birmingham, AL USABoston Univ, Sch Med, Clin Epidemiol Res & Training Unit, Boston, MA 02118 USA