Modulation of established murine collagen-induced arthritis by a single inoculation of short-term lipopolysaccharide-stimulated dendritic cells
Author
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Salazar, L.
Author
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Aravena, O.
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Abello, P.
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Escobar, A.
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Contreras Levicoy, Juan
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Rojas Colonelli, Nicole
Author
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Catalán Martina, Diego
Author
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Aguirre A., Luz María
Author
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Zúñiga, R.
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Pesce Reyes, Bárbara
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González, C.
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Cepeda, R.
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Cuchacovich Turteltaub, Miguel
Author
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Molina, M. C.
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Salazar Onfray, Flavio
Author
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Delgado, M.
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Toes, R. E.
Author
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Aguillón Gutiérrez, Juan Carlos
Admission date
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2019-03-11T12:56:01Z
Available date
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2019-03-11T12:56:01Z
Publication date
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2008
Cita de ítem
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Annals of the Rheumatic Diseases, Volumen 67, Issue 9, 2018, Pages 1235-1241
Identifier
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00034967
Identifier
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10.1136/ard.2007.072199
Identifier
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https://repositorio.uchile.cl/handle/2250/164581
Abstract
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Background: The use of regulatory or immature dendritic cells (DCs) as tools for modulating experimental rheumatoid arthritis is very recent. Tumour necrosis factor (TNF)-stimulated DCs have been shown to restore tolerance in experimental autoimmune encephalomyelitis and collagen-induced arthritis (CIA). Objective: We investigated the capacity of short-term lipopolysacchahde (LPS)-stimulated DCs pulsed with type II collagen (CII) to induce tolerance against established CIA. Methods: Bone marrow-derived DCs were generated in the presence of granulocyte monocyte colony-stimulating factor (GM-CSF). After CIA induction, mice were injected at day 35 with a single dose of 4- or 24-h LPS-stimulated DCs that had been loaded with CII (4hLPS/CII/DCs or 24hLPS/CII/DCs). Arthritis progression was monitored by clinical and histological evaluations. Results: Flow cytometry of 4hLPS/CII/DCs showed intermediate CD40 and CD86 expression, lower than that of 24hLPS/CII/DCs (fully mature) and higher than