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Emerging evidence suggests that the β₂ integrin family of adhesion molecules have an important role in suppressing immune activation and inflammation. β₂ integrins are important adhesion and signalling molecules that are exclusively expressed on leukocytes. The four β₂ integrins (CD11a, CD11b, CD11c and CD11d paired with the β2 chain CD18) play important roles in regulating three key aspects of immune cell function: recruitment to sites of inflammation; cell-cell contact formation; and downstream effects on cellular signalling. Through these three processes, β2 integrins both contribute to and regulate immune responses. This review explores the pro- and anti-inflammatory effects of β₂ integrins in monocytes, macrophages and dendritic cells (DC), and how they influence the outcome of immune responses. We furthermore discuss how imbalances in β₂ integrin function can have far-reaching effects on mounting appropriate immune responses, potentially influencing the development and progression of autoimmune and inflammatory diseases. Therapeutic targeting of β₂ integrins, therefore, holds enormous potential in exploring treatment options for a variety of inflammatory conditions.
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Schittenhelm et al. (Wed,) studied this question.
synapsesocial.com/papers/6a0dca2de51d8d6d0c09d73c — DOI: https://doi.org/10.3389/fimmu.2017.01866
Leonie Schittenhelm
Versus Arthritis
Catharien M. U. Hilkens
NIHR Newcastle Biomedical Research Centre
Vicky L. Morrison
University of Dundee
ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam)
Frontiers in Immunology
University of Glasgow
Newcastle University
Versus Arthritis
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