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Open Access Research article

Folate-targeted immunotherapy effectively treats established adjuvant and collagen-induced arthritis

Chrystal M Paulos1, Bindu Varghese1, William R Widmer2, Gert J Breur2, Erina Vlashi1 and Philip S Low1*

  • * Corresponding author: Philip S Low plow@purdue.edu

  • † Equal contributors

Author Affiliations

1 Department of Chemistry, 560 Oval Drive, 1393 Brown Bldg., Purdue University, West Lafayette, IN 47907-1175, USA

2 Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Purdue University, West Lafayette, IN 47907-1175, USA

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Arthritis Research & Therapy 2006, 8:R77  doi:10.1186/ar1944

Published: 28 April 2006

Abstract

Activated macrophages express a cell surface receptor for the vitamin folic acid. Because this receptor is inaccessible or not measurably expressed on other normal cells, folic acid has been recently exploited to selectively deliver attached radio-emitters to sites of activated macrophage accumulation, allowing scintigraphic imaging of inflamed joints and organs of arthritic rats. We demonstrate here that folate-linked haptens can also be targeted to activated macrophages, decorating their cell surfaces with highly immunogenic molecules. Under conditions in which the rodent has already been immunized against keyhole limpet hemocyanine-(fluorescein isothiocyanate) FITC, activated macrophages are eliminated. Administration of folate-FITC conjugates to rodents with experimental arthritis attenuates (a) systemic and peri-articular inflammation, (b) bone and cartilage degradation, and (c) arthritis-related body weight loss. Treatment with folate-hapten conjugates is comparable to methotrexate, etanercept, anakinra, and celecoxib at alleviating the symptoms of arthritis. We conclude that reduction of activated macrophages by folate-targeted immunotherapy can ameliorate the symptoms of arthritis in two rodent models of the disease.