Overexpression of CXC Chemokine Ligand 14 Exacerbates Collagen-Induced Arthritis

Department of Immunology, Baylor College of Medicine, Houston, TX 77030, USA.
The Journal of Immunology (Impact Factor: 5.36). 03/2010; 184(8):4455-9. DOI: 10.4049/jimmunol.0900525
Source: PubMed

ABSTRACT CXCL14 is a relatively new chemokine with unidentified receptor and undefined function. Recently, we found that CXCL14 is upregulated in arthritic joints in a mouse model of autoimmune arthritis, collagen-induced arthritis. To examine the role of CXCL14 in the development and pathogenesis of autoimmune arthritis, we have generated transgenic (Tg) mice that overexpress CXCL14 under control of phosphoglycerate kinase promoter. The results showed that CXCL14-Tg mice developed more severe arthritis compared with wild-type controls. The draining lymph nodes of CXCL14-Tg mice were significantly enlarged and contained an increased number of activated T cells, particularly the CD44(+)CD62L(low) effector memory cells. In addition, T cells from CXCL14-Tg mice exhibited an enhanced proliferative response against collagen II and produced higher levels of IFN-gamma but not IL-4 or IL-17. CXCL14-Tg mice also had elevated levels of IgG2a autoantibodies. These findings indicated that CXCL14 plays an important role in the autoimmune arthritis, which may have an implication in understanding the pathogenic mechanisms of rheumatoid arthritis in humans and, ultimately, therapeutic interference.

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Available from: Shuhua Han, Mar 17, 2015
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    • "Though its receptor is unknown, CXCL14 is upregulated in inflamed joints of collagen-induced arthritis in mice (Booth et al., 2008). CXCL14 transgenic mice develop more severe arthritis, indicating that CXCL14 may play a role in RA (Chen et al., 2010b). In addition to T cells, B cells are also thought to play a role in RA. "
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