Volume 120, Issue 3 pp. 532-536

CD8+ cells suppress oil-induced arthritis

Å. M. Jansson

Å. M. Jansson

Department of Medicine, Unit of Rheumatology, Karolinska Institute, Stockholm, and

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J. C. Lorentzen

J. C. Lorentzen

Department of Medicine, Unit of Rheumatology, Karolinska Institute, Stockholm, and

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A. Bucht

A. Bucht

Department of Medicine, Unit of Rheumatology, Karolinska Institute, Stockholm, and

Department of Biomedicine, Defence Research Establishment, Umeå, Sweden

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First published: 24 December 2001
Citations: 9
:Åsa Jansson, Centre for Molecular Medicine L8:04, Karolinska Hospital, S-171 76 Stockholm, Sweden.E-mail: [email protected]

Abstract

Oil-induced arthritis is a genetically restricted polyarthritis that develops in the DA rat after injection of the mineral oil Freund's incomplete adjuvant. Here, we investigated the role of the potentially disease-limiting cell populations CD8+ T cells, γδ T cells, natural killer (NK) cells and NK T cells in inguinal lymph nodes for the development of this adjuvant-induced arthritis. Flow cytometry analysis before and at disease onset revealed a higher proportion of lymph node T cells expressing NKR-P1 in the disease-resistant LEW.1AV1 compared with the disease-susceptible DA strain, suggesting that NK T cells might be disease protective. However, prophylactic in vivo administration of an anti-NKR-P1 MoAb (clone 10/78) did not consistently affect the disease course. The proportion of CD8+ T cells and the ratio CD4+/CD8+ T cells in inguinal lymph nodes did not differ significantly between DA and LEW.1AV1 rats before or at disease onset. Nevertheless, prophylactic in vivo depletion of CD8+ cells by the OX8 MoAb in the DA strain resulted in an earlier disease onset compared with the control group, demonstrating that CD8+ cells regulate arthritis development. In vivo depletion of γδ T cells by the V65 MoAb did not alter the disease course, indicating that the disease-suppressive CD8+ cells are αβ T cells or NK cells.

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