The Role of NKG2D and Its Ligands in Autoimmune Diseases: New Targets for Immunotherapy.
Leiyan WeiZhiqing XiangYizhou ZouPublished in: International journal of molecular sciences (2023)
Natural killer (NK) cells and CD8 + T cells can clear infected and transformed cells and generate tolerance to themselves, which also prevents autoimmune diseases. Natural killer group 2 member D (NKG2D) is an important activating immune receptor that is expressed on NK cells, CD8 + T cells, γδ T cells, and a very small percentage of CD4 + T cells. In contrast, the NKG2D ligand (NKG2D-L) is generally not expressed on normal cells but is overexpressed under stress. Thus, the inappropriate expression of NKG2D-L leads to the activation of self-reactive effector cells, which can trigger or exacerbate autoimmunity. In this review, we discuss the role of NKG2D and NKG2D-L in systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), multiple sclerosis (MS), type I diabetes (T1DM), inflammatory bowel disease (IBD), and celiac disease (CeD). The data suggest that NKG2D and NKG2D-L play a pathogenic role in some autoimmune diseases. Therefore, the development of strategies to block the interaction of NKG2D and NKG2D-L may have therapeutic effects in some autoimmune diseases.
Keyphrases
- nk cells
- multiple sclerosis
- induced apoptosis
- rheumatoid arthritis
- natural killer cells
- cell cycle arrest
- celiac disease
- type diabetes
- systemic lupus erythematosus
- signaling pathway
- poor prognosis
- oxidative stress
- cardiovascular disease
- disease activity
- magnetic resonance
- magnetic resonance imaging
- metabolic syndrome
- endoplasmic reticulum stress
- systemic sclerosis
- machine learning
- insulin resistance
- ulcerative colitis
- binding protein
- adipose tissue
- contrast enhanced
- interstitial lung disease
- ms ms