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The Journal of Immunology, 2003, 171: 893-901.
Copyright © 2003 by The American Association of Immunologists

Susceptibility to Experimental Lyme Arthritis Correlates with KC and Monocyte Chemoattractant Protein-1 Production in Joints and Requires Neutrophil Recruitment Via CXCR21

Charles R. Brown2,*,{dagger}, Victoria A. Blaho* and Christie M. Loiacono{dagger}

Departments of * Molecular Microbiology and Immunology and {dagger} Veterinary Pathobiology, University of Missouri, Columbia, MO 65211

The development of experimental Lyme arthritis has been correlated with the expression of a number of chemokines and cytokines, however, none of these have been measured directly from the arthritic joint. We examined the temporal expression of IL-1{beta}, IL-4, IL-6, IL-10, IL-12p70, GM-CSF, IFN-{gamma}, TNF-{alpha}, macrophage inflammatory protein-2, KC, macrophage inflammatory protein-1{alpha}, and monocyte chemoattractant protein-1 directly from the tibiotarsal joint in arthritis-resistant C57BL/6 (B6) and -susceptible C3H/He (C3H) mice. Only the chemokines KC and monocyte chemoattractant protein-1 were differentially expressed in joints of B6 and C3H mice and correlated with the development of Lyme arthritis. Infection of CXCR2-/- mice on either genetic background resulted in a significant decrease in the development of pathology, although infection of CCR2-/- mice had little or no effect. Neutrophils in CXCR2-/- mice were marginalized within blood vessels and could not enter the joint tissue. These results suggest that chemokine-mediated recruitment of neutrophils into the infected joint is a key requirement for the development of experimental Lyme arthritis.




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