Recombinant soluble human FcgammaR1A (CD64A) reduces inflammation in murine collagen-induced arthritis - PubMed (original) (raw)
. 2009 Jun 1;182(11):7272-9.
doi: 10.4049/jimmunol.0803497.
Nels Hamacher, Brandon Harder, Ken Bannink, Thomas R Bukowski, Kelly Byrnes-Blake, Sara Underwood, Colleen Oliver, Kimberly S Waggie, Claire Noriega, LuAnne Hebb, Mark W Rixon, Katherine E Lewis
Affiliations
- PMID: 19454724
- DOI: 10.4049/jimmunol.0803497
Recombinant soluble human FcgammaR1A (CD64A) reduces inflammation in murine collagen-induced arthritis
Jeff L Ellsworth et al. J Immunol. 2009.
Abstract
Binding of immune complexes to cellular FcgammaRs can promote cell activation and inflammation. In previous studies, a recombinant human (rh) soluble FcgammaR, rh-FcgammaRIA (CD64A), was shown to block inflammation in passive transfer models of immune complex-mediated disease. To assess whether rh-FcgammaRIA could block inflammation in a T cell- and B cell-dependent model of immune complex-mediated disease, the efficacy of rh-FcgammaRIA in collagen-induced arthritis was evaluated. Mice with established arthritis were treated with a single s.c. injection of rh-FcgammaRIA (0.2-2.0 mg/dose) given every other day for 11 days. Relative to mice injected with vehicle alone, mice treated with rh-FcgammaRIA exhibited lower serum concentrations of IL-6, anti-type II collagen Abs, and total IgG2a. These changes were correlated with lower levels of paw swelling and joint damage in the rh-FcgammaRIA-treated mice and occurred in the presence of a significant murine Ab response to rh-FcgammaRIA. Comparison of the serum rh-FcgammaRIA concentration vs time profiles for rh-FcgammaRIA administered at two dose levels by i.v. and s.c. injection revealed that the bioavailabilty of s.c. administered rh-FcgammaRIA was 27-37%. Taken together, these data show that rh-FcgammaRIA is an effective inhibitor of inflammation in a model of established arthritis in mice.
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