Anti-CD200R ameliorates collagen-induced arthritis in mice

Immunization of DBA/1 with 100 microg bovine collagen type II emulsified in Freund's adjuvant, followed by booster injection in incomplete adjuvant at 18 days, leads to development of arthritis in more than 70% of mice by 28 days postinjection. We have previously shown that the novel immunosupp...

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Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 104(2002), 3 vom: 01. Sept., Seite 256-64
1. Verfasser: Gorczynski, Reginald M (VerfasserIn)
Weitere Verfasser: Chen, Zhiqi, Lee, Lydia, Yu, Kai, Hu, Jiang
Format: Aufsatz
Sprache:English
Veröffentlicht: 2002
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Antibodies, Monoclonal Antigens, CD Antigens, Surface Autoantibodies Immunoglobulin Fc Fragments Receptors, Immunologic Tumor Necrosis Factor-alpha Interferon-gamma mehr... 82115-62-6 Collagen 9007-34-5 antigens, CD200 UQ4V77A8VA
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245 1 0 |a Anti-CD200R ameliorates collagen-induced arthritis in mice 
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520 |a Immunization of DBA/1 with 100 microg bovine collagen type II emulsified in Freund's adjuvant, followed by booster injection in incomplete adjuvant at 18 days, leads to development of arthritis in more than 70% of mice by 28 days postinjection. We have previously shown that the novel immunosuppressant molecule CD200Fc (linking an extracellular domain of CD200 with a murine IgG2a Fc region) can suppress induction of disease when given to mice from the time of collagen injection. This occurs in concert with a decrease in the serum levels of anti-collagen IgG ( approximately 50% reduction), with relatively more IgG2b and IgG3, decreased serum levels of TNFalpha and IFN-gamma, and decreased production of those same cytokines after restimulation of lymphocytes in vitro with collagen. Since CD200 induces suppression following engagement of a receptor (CD200R), known to be expressed on, among other cells, macrophages, we investigated whether infusion of anti-CD200R and/or CD200Fc would ameliorate established disease in DBA mice, when injections were begun following collagen immunization. Our data indicate an arrest of disease following either treatment, with modification of a number of immune parameters (serum and lymphocyte cytokine production) consistent with a general role for CD200:CD200R interactions in the regulation of induction and/or expression of autoimmune disorders. When a higher dose (250 microg/mouse) of anti-CD200R was infused into a group of overtly arthritic mice, a significant ( approximately 50%) decrease in arthritic joint score occurred over the 4-week treatment period 
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650 7 |a Antigens, Surface  |2 NLM 
650 7 |a Autoantibodies  |2 NLM 
650 7 |a Immunoglobulin Fc Fragments  |2 NLM 
650 7 |a Receptors, Immunologic  |2 NLM 
650 7 |a Tumor Necrosis Factor-alpha  |2 NLM 
650 7 |a Interferon-gamma  |2 NLM 
650 7 |a 82115-62-6  |2 NLM 
650 7 |a Collagen  |2 NLM 
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650 7 |a antigens, CD200  |2 NLM 
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700 1 |a Chen, Zhiqi  |e verfasserin  |4 aut 
700 1 |a Lee, Lydia  |e verfasserin  |4 aut 
700 1 |a Yu, Kai  |e verfasserin  |4 aut 
700 1 |a Hu, Jiang  |e verfasserin  |4 aut 
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