Dendritic Cells and CCR7 Expression: An Important Factor for Autoimmune Diseases, Chronic Inflammation, and Cancer

被引:78
作者
Brandum, Emma Probst [1 ]
Jorgensen, Astrid Sissel [1 ]
Rosenkilde, Mette Marie [1 ]
Hjorto, Gertrud Malene [1 ]
机构
[1] Fac Hlth & Med Sci, Dept Biomed Sci, Blegdamsvej 3B,Room 18-5-32, DK-2200 Copenhagen, Denmark
关键词
dendritic cell; CCR7; chronic inflammation; MS; RA; psoriasis; cancer; CHEMOKINE RECEPTOR CCR7; LYMPH-NODE METASTASIS; MULTIPLE-SCLEROSIS PATIENTS; HEMATOPOIETIC STEM-CELLS; CENTRAL-NERVOUS-SYSTEM; CD4(+) T-CELLS; RHEUMATOID-ARTHRITIS; ANTITUMOR RESPONSES; SKIN INFLAMMATION; STEADY-STATE;
D O I
10.3390/ijms22158340
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chemotactic cytokines-chemokines-control immune cell migration in the process of initiation and resolution of inflammatory conditions as part of the body's defense system. Many chemokines also participate in pathological processes leading up to and exacerbating the inflammatory state characterizing chronic inflammatory diseases. In this review, we discuss the role of dendritic cells (DCs) and the central chemokine receptor CCR7 in the initiation and sustainment of selected chronic inflammatory diseases: multiple sclerosis (MS), rheumatoid arthritis (RA), and psoriasis. We revisit the binary role that CCR7 plays in combatting and progressing cancer, and we discuss how CCR7 and DCs can be harnessed for the treatment of cancer. To provide the necessary background, we review the differential roles of the natural ligands of CCR7, CCL19, and CCL21 and how they direct the mobilization of activated DCs to lymphoid organs and control the formation of associated lymphoid tissues (ALTs). We provide an overview of DC subsets and, briefly, elaborate on the different T-cell effector types generated upon DC-T cell priming. In the conclusion, we promote CCR7 as a possible target of future drugs with an antagonistic effect to reduce inflammation in chronic inflammatory diseases and an agonistic effect for boosting the reactivation of the immune system against cancer in cell-based and/or immune checkpoint inhibitor (ICI)-based anti-cancer therapy.
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页数:24
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