Chemokine (C–X–C motif) ligand (CXCL)10 in autoimmune diseases
Abstract
(C-X-C motif) ligand (CXCL)10 (CXCL10) belongs to the ELR(-) CXC subfamily chemokine. CXCL10 exerts its function through binding to chemokine (C-X-C motif) receptor 3 (CXCR3), a seven trans-membrane receptor coupled to G proteins. CXCL10 and its receptor, CXCR3, appear to contribute to the pathogenesis of many autoimmune diseases, organ specific (such as type 1 diabetes, autoimmune thyroiditis, Graves' disease and ophthalmopathy), or systemic (such as rheumatoid arthritis, psoriatic arthritis, systemic lupus erythematosus, mixed cryoglobulinemia, Sjögren syndrome, or systemic sclerosis). The secretion of CXCL10 by cluster of differentiation (CD)4+, CD8+, natural killer (NK) and NK-T cells is dependent on interferon (IFN)-γ, which is itself mediated by the interleukin-12 cytokine family. Under the influence of IFN-γ, CXCL10 is secreted by several cell types including endothelial cells, fibroblasts, keratinocytes, thyrocytes, preadipocytes, etc. Determination of high level of CXCL10 in peripheral fluids is therefore a marker of host immune response, especially T helper (Th)1 orientated T-cells. In tissues, recruited Th1 lymphocytes may be responsible for enhanced IFN-γ and tumor necrosis factor-α production, which in turn stimulates CXCL10 secretion from a variety of cells, therefore creating an amplification feedback loop, and perpetuating the autoimmune process. Further studies are needed to investigate interactions between chemokines and cytokines in the pathogenesis of auto…
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Many of the changes in the circulating proteome in people with Down syndrome are highly reminiscent of those observed in type I interferonopathies and other autoinflammatory conditions.
“Our study of the circulating proteome in people with DS, the largest and most comprehensive study of this kind reported to date, reveals that T21 causes profound immune dysregulation, with many of the changes being highly reminiscent of those observed in type I interferonopathies and other autoinflammatory conditions54,58–60,88 (Table 1).”
From Trisomy 21 causes changes in the circulating proteome indicative of chronic autoinflammation (2017) · cites this paper as [88]
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Trisomy 21 causes changes in the circulating proteome indicative of chronic autoinflammation
Sullivan, K. D., Evans, D., Pandey, A., Hraha, T. H., Smith, K. P., Markham, N., Rachubinski, A. L., Wolter-Warmerdam, K., Hickey, F., Espinosa, J. M., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-13858-3 · Cited by 228 · see citing works
Fleischmann, R. M., Wagner, F., Kivitz, A. J., Mansikka, H. T., Khan, N., Othman, A. A., Khatri, A., Hong, F., Jiang, P., Ruzek, M., et al. (2017) · Arthritis & Rheumatology · doi:10.1002/art.40319 · Cited by 32 · see citing works
Meyer, J. D., Hayney, M. S., Coe, C. L., Ninos, C. L., & Barrett, B. P. (2019) · Journal of Sport and Exercise Psychology · doi:10.1123/jsep.2018-0214 · Cited by 29 · see citing works
- Authors
- Antonelli, A., Ferrari, S. M., Giuggioli, D., Ferrannini, E., Ferri, C., & Fallahi, P.
- Affiliations
- University of Pisa (IT)
- University of Modena and Reggio Emilia (IT)
- Corresponding author
- Antonelli, Alessandro
- Venue
- Autoimmunity Reviews
- Publisher
- Elsevier BV
- Published
- 2014-03
- Volume
- 13
- Issue
- 3
- Pages
- 272-280
- ISSN
- 1568-9972 (ISSN-L)
- OpenAlex
- W2006821600
- Cited by
- 595
- References
- 3
- Citations by year
- 2026: 33 · 2025: 53 · 2024: 62 · 2023: 50 · 2022: 53 · 2021: 56 · 2020: 45 · 2019: 35 · 2018: 35 · 2017: 51 · 2016: 46 · 2015: 41 · 2014: 34
- FWCI
- 4.26
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Autoimmunity Reviews (publishedVersion)
- PubMed (publishedVersion)
- CINECA IRIS Institutial research information system (University of Pisa) (submittedVersion)
- IRIS UNIMORE (University of Modena and Reggio Emilia) (submittedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Chemokine receptors and signaling
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
- Keywords
- CXCL10, CXCR3, chemokines, autoimmune disease, interferon-gamma, Th1 cells, IL-12, type 1 diabetes, autoimmune thyroiditis, Graves' disease, rheumatoid arthritis, systemic lupus erythematosus, Sjögren's syndrome, systemic sclerosis, mixed cryoglobulinemia, biomarkers, therapeutic target
- MeSH terms
- Animals, Autoimmune Diseases, Humans, Inflammation, Ligands, Chemokine CXCL10, Receptors, CXCR3
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