Cancer treatment and the KIR-HLA system: an overview.
Patrizia LeoneValli De ReAngelo VaccaFranco DammaccoVito RacanelliPublished in: Clinical and experimental medicine (2017)
Accumulating evidence indicates that the success of cancer therapy depends not only on a combination of adequate procedures (surgery, chemotherapy and radiotherapy) that aim to eliminate all tumor cells, but also on the functional state of the host immune system. HLA and KIR molecules, in particular, are critical to the interactions between tumor cells and both innate and adaptive immune cells such as NK cells and T cells. Different KIR-HLA gene combinations as well as different HLA expression levels on tumor cells associate with variable tumor prognosis and response to treatment. On the other hand, different therapies have different effects on HLA molecules and immune cell functions regulated by these molecules. Here, we provide an overview of the KIR-HLA system, a description of its alterations with clinical relevance in diverse tumor types, and an analysis of the consequences that conventional cancer therapies may have on it. We also discuss how this knowledge can be exploited to identify potential immunological biomarkers that can help to select patients for tailored therapy.
Keyphrases
- cancer therapy
- end stage renal disease
- immune response
- nk cells
- newly diagnosed
- early stage
- chronic kidney disease
- ejection fraction
- locally advanced
- stem cells
- squamous cell carcinoma
- genome wide
- prognostic factors
- dna methylation
- peritoneal dialysis
- binding protein
- risk assessment
- coronary artery disease
- mesenchymal stem cells
- climate change
- radiation induced
- coronary artery bypass
- long non coding rna
- percutaneous coronary intervention
- cell therapy
- combination therapy