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The Role of M1/M2 Macrophage Polarization in Rheumatoid Arthritis Synovitis
Open accessAbstract
Innate and adaptive immunity represent a harmonic counterbalanced system involved in the induction, progression, and possibly resolution of the inflammatory reaction that characterize autoimmune rheumatic diseases (ARDs), including rheumatoid arthritis (RA). Although the immunopathophysiological mechanisms of the ARDs are not fully clarified, they are often associated with an inappropriate macrophage/T-cell interaction, where classical (M1) or alternative (M2) macrophage activation may influence the occurrence of T-helper (Th)1 or Th2 responses. In RA patients, M1/Th1 activation occurs in an inflammatory environment dominated by Toll-like receptor (TLR) and interferon (IFN) signaling, and it promotes a massive production of pro-inflammatory cytokines [i.e., tumor necrosis factor-α (TNFα), interleukin (IL)-1, IL-12, IL-18, and IFNγ], chemotactic factors, and matrix metalloproteinases resulting in osteoclastogenesis, erosion, and progressive joint destruction. On the other hand, the activation of M2/Th2 response determines the release of growth factors and cytokines [i.e., IL-4, IL-10, IL-13, and transforming growth factor (TGF)-β] involved in the anti-inflammatory process leading to the clinical remission of RA. Several subtypes of macrophages have been described. Five polarization states from M1 to M2 have been confirmed in in vitro studies analyzing morphological characteristics, gene expression of phenotype markers (CD80, CD86, TLR2, TLR4, or CD206, CD204, CD163, MerTK), and functional aspect, including the production of reactive oxygen species (ROS). An M1 and M2 macrophage imbalance may induce pathological consequences and contribute to several diseases, such as asthma or osteoclastogenesis in RA patients. In addition, the macrophage dynamic polarization from M1 to M2 includes the presence of intermediate polarity stages distinguished by the expression of specific surface markers and the production/release of distinct molecules (i.e., nitric oxide, cytokines), which characterize their morphological and functional state. This suggests a “continuum” of macrophage activation states playing an important role during inflammation and its resolution. This review discusses the importance of the delicate M1/M2 imbalance in the different phases of the inflammatory process together with the identification of specific pathways, cytokines, and chemokines involved, and its clinical outcomes in RA. The analysis of these aspects could shed a light on the abnormal inflammatory activation, leading to novel therapeutical approaches which may contribute to restore the M1/M2 balance.
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Cites
Exploring the full spectrum of macrophage activation
Mosser, D. M., & Edwards, J. P. (2008) · Nature Reviews Immunology · doi:10.1038/nri2448 · Cited by 9,144 · cited 1×
“Indeed, plasticity is a key feature also of macrophages, which are capable of presenting heterogeneous phenotypes creating various subpopulations; therefore, these cells are not only involved in the propagation of inflammation but also in its resolution, depending on their activation state (M1 or M2) (37).”
BackgroundThe chemokine system in diverse forms of macrophage activation and polarization
MANTOVANI, A., SICA, A., SOZZANI, S., ALLAVENA, P., VECCHI, A., & LOCATI, M. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.09.015 · Cited by 6,534
The Pathogenesis of Rheumatoid Arthritis
McInnes, I. B., & Schett, G. (2011) · New England Journal of Medicine · doi:10.1056/nejmra1004965 · Cited by 5,514 · cited 1×
“Although RA pathophysiology remains elusive, the presence of a complex interplay among genotype, epigenetic changes, and environmental factors underlying chronic inflammation is abundantly described (7, 8).”
BackgroundMacrophage biology in development, homeostasis and disease
Wynn, T. A., Chawla, A., & Pollard, J. W. (2013) · Nature · doi:10.1038/nature12034 · Cited by 4,684 · cited 1×
“org 4 maturation; this is a fundamental function in the regulation of inflammation and in the maintenance of homeostasis (35, 36).”
BackgroundSuccinate is an inflammatory signal that induces IL-1β through HIF-1α
Tannahill, G. M., Curtis, A. M., Adamik, J., Palsson-McDermott, E. M., McGettrick, A. F., Goel, G., Frezza, C., Bernard, N. J., Kelly, B., Foley, N. H., et al. (2013) · Nature · doi:10.1038/nature11986 · Cited by 4,176
Evolving concepts of rheumatoid arthritis
Firestein, G. S. (2003) · Nature · doi:10.1038/nature01661 · Cited by 3,605
Macrophage Cytokines: Involvement in Immunity and Infectious Diseases
Arango Duque, G., & Descoteaux, A. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00491 · Cited by 2,708
Nomenclature of monocytes and dendritic cells in blood
Ziegler-Heitbrock, L., Ancuta, P., Crowe, S., Dalod, M., Grau, V., Hart, D. N., Leenen, P. J. M., Liu, Y.-J., MacPherson, G., Randolph, G. J., et al. (2010) · Blood · doi:10.1182/blood-2010-02-258558 · Cited by 2,436
Rheumatoid arthritis: pathological mechanisms and modern pharmacologic therapies
Guo, Q., Wang, Y., Xu, D., Nossent, J., Pavlos, N. J., & Xu, J. (2018) · Bone Research · doi:10.1038/s41413-018-0016-9 · Cited by 1,767
Identification of the haemoglobin scavenger receptor
Kristiansen, M., Graversen, J. H., Jacobsen, C., Sonne, O., Hoffman, H.-J., Law, S. K. A., & Moestrup, S. K. (2001) · Nature · doi:10.1038/35051594 · Cited by 1,712
Research works printed but not linked: 16
- Siddle, 2014, Anatomical Location of Erosions at the Metatarsophalangeal Joints in Patients With Rheumatoid Arthritis, Rheumatology, 53, 10.1093/rheumatology/ket478 · doi:10.1093/rheumatology/ket478
- Turesson, 2013, Extra-Articular Rheumatoid Arthritis, Curr, Opin Rheumatol, 25, 10.1097/BOR.0b013e32835f693f · doi:10.1097/bor.0b013e32835f693f
- Alex, 2020, Exposure to Ambient Air Pollution and Autoantibody Status in Rheumatoid Arthritis, Clin Rheumatol, 39, 10.1007/s10067-019-04813-w · doi:10.1007/s10067-019-04813-w
- Weldon, 2015, Surface APRIL Is Elevated on Myeloid Cells and Is Associated With Disease Activity in Patients With Rheumatoid Arthritis, J Rheumatol, 42, 10.3899/jrheum.140630 · doi:10.3899/jrheum.140630
- Crilly, 2012, PAR(2) Expression in Peripheral Blood Monocytes of Patients With Rheumatoid Arthritis, Ann Rheum Dis, 71, 10.1136/annrheumdis-2011-200703 · doi:10.1136/annrheumdis-2011-200703
- Ellingsen, 2014, Upregulated Baseline Plasma CCL19 and CCR7 Cell-Surface Expression on Monocytes in Early Rheumatoid Arthritis Normalized During Treatment and CCL19 Correlated With Radiographic Progression, Scand J Rheumatol, 43, 91, 10.3109/03009742.2013.803149 · doi:10.3109/03009742.2013.803149
- Cutolo, 2013, Intracellular NF-kB-Decrease and IKBalpha Increase in Human Macrophages Following CTLA4-Ig Treatment, Clin Exp Rheumatol, 31
- Brizzolara, 2013, Rapid Interaction Between CTLA4-Ig (Abatacept) and Synovial Macrophages From Patients With Rheumatoid Arthritis, J Rheumatol, 40, 10.3899/jrheum.120866 · doi:10.3899/jrheum.120866
- Schett, 2000, Activation, Differential Localization, and Regulation of the Stress-Activated Protein Kinases, Extracellular Signal-Regulated Kinase, C-JUN N-Terminal Kinase, and P38 Mitogen-Activated Protein Kinase, in Synovial Tissue and Cells in Rheumatoid Arthritis, Arthritis Rheumatol, 43, 10.1002/1529-0131(200011)43:11<2501::AID-ANR18>3.0.CO;2-K · doi:10.1002/1529-0131(200011)43:11<2501::aid-anr18>3.0.co;2-k
- Salisbury, 1987, Macrophage-Like Cells of the Pannus Area in Rheumatoid Arthritic Joints, Scand J Rheumatol, 16, 10.3109/03009748709102927 · doi:10.3109/03009748709102927
- Combe, 2015, Comparison of the Long-Term Outcome for Patients With Rheumatoid Arthritis With Persistent Moderate Disease Activity or Disease Remission During the First Year After Diagnosis: Data From the ESPOIR Cohort, Ann Rheum Dis, 74, 10.1136/annrheumdis-2013-204178 · doi:10.1136/annrheumdis-2013-204178
- Obeng, 2016, Modulation of Human Monocyte/Macrophage Activity by Tocilizumab, Abatacept and Etanercept: An In Vitro Study, Eur J Pharmacol, 780, 10.1016/j.ejphar.2016.03.028 · doi:10.1016/j.ejphar.2016.03.028
- Schatz, 2016, Resolution of Pericardial Constriction With Anakinra in a Patient With Effusive-Constrictive Pericarditis Secondary to Rheumatoid Arthritis, Int J Cardiol, 223, 10.1016/j.ijcard.2016.08.131 · doi:10.1016/j.ijcard.2016.08.131
- Weisman, 2006, Reduction of Inflammatory Biomarker Response by Abatacept in Treatment of Rheumatoid Arthritis, J Rheumatol, 33
- Cutolo, 2016, Effects of Combined Treatments With CTLA4-IG (Abatacept), Dexamethasone and Methotrexate on Cultured Human Macrophages, Clin Exp Rheumatol, 34
- Cutolo, 2018, Testing the Anti-Osteoclastic Function of Biological DMARDs, Nat Rev Rheumatol, 14, 10.1038/s41584-018-0046-0 · doi:10.1038/s41584-018-0046-0
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Breaking Boundaries: Chronic Diseases and the Frontiers of Immune Microenvironments
Li, G., Wan, Y., Jiao, A., Jiang, K., Cui, G., Tang, J., Yu, S., Hu, Z., Zhao, S., Yi, Z., et al. (2025) · Med Research · doi:10.1002/mdr2.70007 · Cited by 63
Jiang, W., Liu, Y., Wu, Y., Zhang, L., Zhang, B., Zhou, S., Zhang, P., Xu, T., Wu, M., & Lv, S. (2024) · Scientific Reports · doi:10.1038/s41598-024-67289-y · Cited by 50
Zhou, J., Luo, W., Xie, Z., Xia, C., & Zhao, J. (2024) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.23816 · Cited by 7
Kalidass, B., Murugesan, K., Shanmugam, A., Kaveri, P. K., & Lakshmanan, D. K. (2026) · Cellular Immunology · doi:10.1016/j.cellimm.2026.105129
Metadata
- Authors
- Cutolo, M., Campitiello, R., Gotelli, E., & Soldano, S.
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2022-05-19
- Volume
- 13
- Pages
- 867260-867260
- ISSN
- 1664-3224 (ISSN-L)
- OpenAlex
- W4280542784
- Cited by
- 631
- References
- 95
- FWCI
- 75.04
- Type
- journal article
- Language
- en
- Open access
- gold
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