Macrophage polarization in spondyloarthritis

Introduction : Synovial tissue macrophages play a key role in chronic inflammatory arthritis, but the contribution of different macrophage subsets in this process remains largely unknown. The main in vitro polarized macrophage subsets are classically (M1) and alternatively (M2) activated macrophages, the latter comprising interleukin (IL)-4 and IL-10 polarized cells. Here, we aimed to evaluate the polarization status of synovial macrophages in spondyloarthritis (SpA) and rheumatoid arthritis (RA). Methods: Expression of polarization markers on synovial macrophages, peripheral blood monocytes, and in vitro polarized monocyte-derived macrophages from SpA versus RA patients was assessed by immunohistochemistry and flow cytometry, respectively. The polarization status of the intimal lining layer and the synovial sublining macrophages was assessed by double immunofluorescence staining. Results: The expression of the IL-10 polarization marker cluster of differentiation 163 (CD163) was increased in SpA compared with RA intimal lining layer, but no differences were found in other M1 and M2 markers between the diseases. Furthermore, no significant phenotypic differences in monocytes and in vitro polarized monocyte-derived macrophages were seen between SpA, RA, and healthy controls, indicating that the differential CD163 expression does not reflect a preferential M2 polarization in SpA. More detailed analysis of intimal lining layer macrophages revealed a strong co-expression of the IL-10 polarization markers CD163 and cluster of differentiation 32 (CD32) but not any of the other markers in both SpA and RA. In contrast, synovial sublining macrophages had a more heterogeneous phenotype, with a majority of cells co-expressing M1 and M2 markers. Conclusion: The intimal lining layer but not synovial sublining macrophages display an IL-10 polarized-like phenotype, with increased CD163 expression in SpA versus RA synovitis. These differences in the distribution of the polarized macrophage subset may contribute to the outcome of chronic synovitis.

[1]  T. Wynn,et al.  Protective and pathogenic functions of macrophage subsets , 2011, Nature Reviews Immunology.

[2]  A. Mantovani,et al.  Cancer‐promoting tumor‐associated macrophages: New vistas and open questions , 2011, European journal of immunology.

[3]  A. Chawla,et al.  Alternative macrophage activation and metabolism. , 2011, Annual review of pathology.

[4]  C. Peterson,et al.  Adipose tissue macrophages in insulin resistant subjects are 1 associated with collagen VI, fibrosis and demonstrate 2 alternative activation , 2010 .

[5]  P. Tak,et al.  Evaluating antirheumatic treatments using synovial biopsy: a recommendation for standardisation to be used in clinical trials , 2010, Annals of the rheumatic diseases.

[6]  J. Casanova,et al.  Human CD14dim Monocytes Patrol and Sense Nucleic Acids and Viruses via TLR7 and TLR8 Receptors , 2010, Immunity.

[7]  P. Gimotty,et al.  Hypoxia-inducible factor 2alpha regulates macrophage function in mouse models of acute and tumor inflammation. , 2010, The Journal of clinical investigation.

[8]  H. Wilson Macrophages heterogeneity in atherosclerosis – implications for therapy , 2010, Journal of cellular and molecular medicine.

[9]  Steven J. M. Jones,et al.  Tumor-associated macrophages and survival in classic Hodgkin's lymphoma. , 2010, The New England journal of medicine.

[10]  J. Joyce,et al.  IL-4 induces cathepsin protease activity in tumor-associated macrophages to promote cancer growth and invasion. , 2010, Genes & development.

[11]  Olivier Levillain,et al.  Macrophage Plasticity in Experimental Atherosclerosis , 2010, PloS one.

[12]  J. Pablos,et al.  Synovial immunopathological changes associated with successful abatacept therapy in a case of severe refractory psoriatic arthritis , 2009, Annals of the rheumatic diseases.

[13]  E. Pamer,et al.  Distinct Responses of Human Monocyte Subsets to Aspergillus fumigatus Conidia1 , 2009, The Journal of Immunology.

[14]  P. Tak,et al.  The dynamics of macrophage lineage populations in inflammatory and autoimmune diseases. , 2009, Arthritis and rheumatism.

[15]  R. Lutter,et al.  Absence of a classically activated macrophage cytokine signature in peripheral spondylarthritis, including psoriatic arthritis. , 2009, Arthritis and rheumatism.

[16]  J. Edwards,et al.  Exploring the full spectrum of macrophage activation , 2008, Nature Reviews Immunology.

[17]  P. Comoglio,et al.  Tumor angiogenesis and progression are enhanced by Sema4D produced by tumor-associated macrophages , 2008, The Journal of experimental medicine.

[18]  F. Geissmann,et al.  Blood monocytes: distinct subsets, how they relate to dendritic cells, and their possible roles in the regulation of T‐cell responses , 2008, Immunology and cell biology.

[19]  R. Inman,et al.  Gene expression analysis of macrophages derived from ankylosing spondylitis patients reveals interferon-gamma dysregulation. , 2008, Arthritis and rheumatism.

[20]  Stephen W. Waldo,et al.  Heterogeneity of human macrophages in culture and in atherosclerotic plaques. , 2008, The American journal of pathology.

[21]  F. Karpe,et al.  Remodeling Phenotype of Human Subcutaneous Adipose Tissue Macrophages , 2008, Circulation.

[22]  C. Wijbrandts,et al.  Absence of changes in the number of synovial sublining macrophages after ineffective treatment for rheumatoid arthritis: Implications for use of synovial sublining macrophages as a biomarker. , 2007, Arthritis and rheumatism.

[23]  Frank Brombacher,et al.  Macrophage-specific PPARγ controls alternative activation and improves insulin resistance , 2007, Nature.

[24]  G. Zlabinger,et al.  Human adipose tissue macrophages are of an anti-inflammatory phenotype but capable of excessive pro-inflammatory mediator production , 2007, International Journal of Obesity.

[25]  E Crivellato,et al.  Macrophages in rheumatoid arthritis. , 2007, Histology and histopathology.

[26]  L. Ziegler‐Heitbrock,et al.  The CD14+ CD16+ blood monocytes: their role in infection and inflammation , 2007, Journal of leukocyte biology.

[27]  A. Saltiel,et al.  Obesity induces a phenotypic switch in adipose tissue macrophage polarization. , 2007, The Journal of clinical investigation.

[28]  A. Boots,et al.  Synovial inflammation does not change in the absence of effective treatment: implications for the use of synovial histopathology as biomarker in early phase clinical trials in rheumatoid arthritis , 2006, Annals of the rheumatic diseases.

[29]  D. Baeten,et al.  Immunomodulatory effects of etanercept on peripheral joint synovitis in the spondylarthropathies. , 2005, Arthritis and rheumatism.

[30]  D. Foell,et al.  Differential expression and response to anti-TNFalpha treatment of infiltrating versus resident tissue macrophage subsets in autoimmune arthritis. , 2005, The Journal of pathology.

[31]  D. Foell,et al.  Synovial histopathology of psoriatic arthritis, both oligo- and polyarticular, resembles spondyloarthropathy more than it does rheumatoid arthritis , 2005, Arthritis research & therapy.

[32]  D. Baeten,et al.  Infiltration of the synovial membrane with macrophage subsets and polymorphonuclear cells reflects global disease activity in spondyloarthropathy , 2005, Arthritis research & therapy.

[33]  A. Zwinderman,et al.  Synovial tissue macrophages: a sensitive biomarker for response to treatment in patients with rheumatoid arthritis , 2004, Annals of the rheumatic diseases.

[34]  A. Zwinderman,et al.  Effects of oral prednisolone on biomarkers in synovial tissue and clinical improvement in rheumatoid arthritis. , 2004, Arthritis and rheumatism.

[35]  Silvano Sozzani,et al.  The chemokine system in diverse forms of macrophage activation and polarization. , 2004, Trends in immunology.

[36]  D. Baeten,et al.  Histological evidence that infliximab treatment leads to downregulation of inflammation and tissue remodelling of the synovial membrane in spondyloarthropathy , 2004, Annals of the rheumatic diseases.

[37]  S. Moestrup,et al.  Association of CD163+ macrophages and local production of soluble CD163 with decreased lymphocyte activation in spondylarthropathy synovitis. , 2004, Arthritis and rheumatism.

[38]  P. Tak,et al.  Microarchitecture and protective mechanisms in synovial tissue from clinically and arthroscopically normal knee joints , 2003, Annals of the rheumatic diseases.

[39]  L. Joosten,et al.  Increased expression of Fcgamma receptors II and III on macrophages of rheumatoid arthritis patients results in higher production of tumor necrosis factor alpha and matrix metalloproteinase. , 2003, Arthritis and rheumatism.

[40]  Andrew C. Li,et al.  The macrophage foam cell as a target for therapeutic intervention , 2002, Nature Medicine.

[41]  P. Allavena,et al.  Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes. , 2002, Trends in immunology.

[42]  H. Makino,et al.  CD14+,CD16+ blood monocytes and joint inflammation in rheumatoid arthritis. , 2002, Arthritis and rheumatism.

[43]  M. Fishbein,et al.  Overexpression of Interleukin-10 by Activated T Lymphocytes Inhibits Atherosclerosis in LDL Receptor–Deficient Mice by Altering Lymphocyte and Macrophage Phenotypes , 2002, Circulation research.

[44]  T. Espevik,et al.  The Proinflammatory CD14+CD16+DR++ Monocytes Are a Major Source of TNF1 , 2002, The Journal of Immunology.

[45]  A. Bell,et al.  The CD14+ CD16+ monocyte subset in rheumatoid arthritis and systemic lupus erythematosus , 2002, Rheumatology International.

[46]  Martine De Vos,et al.  Cartilage-derived morphogenetic protein-1 and -2 are endogenously expressed and stimulate proteoglycan synthesis in healthy and osteoarthritic human articular chondrocytes , 2001, Arthritis Research.

[47]  B. Bresnihan,et al.  The pathogenesis and prevention of joint damage in rheumatoid arthritis: advances from synovial biopsy and tissue analysis. , 2000, Arthritis and rheumatism.

[48]  T. Langmann,et al.  Regulation of scavenger receptor CD163 expression in human monocytes and macrophages by pro‐ and antiinflammatory stimuli , 2000, Journal of leukocyte biology.

[49]  J. Domínguez,et al.  The porcine 2A10 antigen is homologous to human CD163 and related to macrophage differentiation. , 1999, Journal of immunology.

[50]  N. Van Rooijen,et al.  Local removal of phagocytic synovial lining cells by clodronate-liposomes decreases cartilage destruction during collagen type II arthritis , 1998, Annals of the rheumatic diseases.

[51]  F. Breedveld,et al.  Analysis of the synovial cell infiltrate in early rheumatoid synovial tissue in relation to local disease activity. , 1997, Arthritis and rheumatism.

[52]  M. Ernst,et al.  Differential expression and function of CD80 (B7‐1) and CD86 (B7‐2) on human peripheral blood monocytes , 1996, Immunology.

[53]  S Gordon,et al.  Interleukin 4 potently enhances murine macrophage mannose receptor activity: a marker of alternative immunologic macrophage activation , 1992, The Journal of experimental medicine.

[54]  M. Dougados,et al.  The European Spondylarthropathy Study Group preliminary criteria for the classification of spondylarthropathy. , 1991, Arthritis and rheumatism.

[55]  M. Liang,et al.  The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. , 1988, Arthritis and rheumatism.

[56]  T. Radstake,et al.  UvA-DARE ( Digital Academic Repository ) Macrophage polarization in spondyloarthritis , 2012 .

[57]  P. Tak,et al.  Interleukin-17-positive mast cells contribute to synovial inflammation in spondylarthritis. , 2012, Arthritis and rheumatism.

[58]  S. Gordon Alternative activation of macrophages , 2003, Nature Reviews Immunology.

[59]  M. Vos,et al.  Immunomodulatory effects of anti-tumor necrosis factor alpha therapy on synovium in spondylarthropathy: histologic findings in eight patients from an open-label pilot study. , 2001, Arthritis and rheumatism.

[60]  A. Balsa,et al.  Differential expression of the costimulatory molecules B7.1 (CD80) and B7.2 (CD86) in rheumatoid synovial tissue. , 1996, British journal of rheumatology.