Dendritic cell integrin expression patterns regulate inflammation in the rheumatoid arthritis joint.

Autor:	Schittenhelm L; Institute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, UK.; Translational & Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.; Research into Inflammatory Arthritis Centre Versus Arthritis (RACE), Glasgow, UK., Robertson J; Institute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, UK., Pratt AG; Translational & Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.; Research into Inflammatory Arthritis Centre Versus Arthritis (RACE), Glasgow, UK.; Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., Hilkens CM; Translational & Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.; Research into Inflammatory Arthritis Centre Versus Arthritis (RACE), Glasgow, UK., Morrison VL; Institute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, UK.; Research into Inflammatory Arthritis Centre Versus Arthritis (RACE), Glasgow, UK.
Jazyk:	angličtina
Zdroj:	Rheumatology (Oxford, England) [Rheumatology (Oxford)] 2021 Mar 02; Vol. 60 (3), pp. 1533-1542.
DOI:	10.1093/rheumatology/keaa686
Abstrakt:	Objectives: Immune dysregulation contributes to the development of RA. Altered surface expression patterns of integrin adhesion receptors by immune cells is one mechanism by which this may occur. We investigated the role of β2 integrin subunits CD11a and CD11b in dendritic cell (DC) subsets of RA patients. Methods: Total β2 integrin subunit expression and its conformation ('active' vs 'inactive' state) were quantified in DC subsets from peripheral blood (PB) and SF of RA patients as well as PB from healthy controls. Ex vivo stimulation of PB DC subsets and in vitro-generated mature and tolerogenic monocyte-derived DCs (moDCs) were utilized to model the clinical findings. Integrin subunit contribution to DC function was tested by analysing clustering and adhesion, and in co-cultures to assess T cell activation. Results: A significant reduction in total and active CD11a expression in DCs in RA SF compared with PB and, conversely, a significant increase in CD11b expression was found. These findings were modelled in vitro using moDCs: tolerogenic moDCs showed higher expression of active CD11a and reduced levels of active CD11b compared with mature moDCs. Finally, blockade of CD11b impaired T cell activation in DC-T cell co-cultures. Conclusion: For the first time in RA, we show opposing expression of CD11a and CD11b in DCs in environments of inflammation (CD11alow/CD11bhigh) and steady state/tolerance (CD11ahigh/CD11blow), as well as a T cell stimulatory role for CD11b. These findings highlight DC integrins as potential novel targets for intervention in RA. (© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Rheumatology.)
Databáze:	MEDLINE
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