Immune checkpoints in hematologic malignancies: What made the immune cells and clinicians exhausted!
Abbas HajifathaliSayeh ParkhidehMohammad Hossein KazemiRouzbeh ChegeniElham RoshandelMajid GholizadehPublished in: Journal of cellular physiology (2020)
Hematologic malignancies comprise a considerable part of cancers with high mortality at any age. Since the introduction of hematopoietic stem cell transplantation (HSCT), the overall survival of patients dramatically increased. The main goal of HSCT is the induction of a graft-versus-leukemia effect to eradicate the residual cancer cells and also reconstitute a healthy immune system for patients. However, relapse is a nettlesome challenge of HSCT. Like many other tumors, hematologic cancer cells induce immune exhaustion leading to immune escape and relapses after HSCT. Besides malignant cells, inhibitory cells such as tumor-associated macrophages and myeloid-derived suppressor cells express various inhibitory receptors capable of inducing exhaustion in immune cells, especially T and natural killer cells. The significance of immune checkpoint blocking in tumor regression in clinical trials led to the 2018 Nobel Prize in Physiology/Medicine. Here, we reviewed the clinical roles of immune checkpoints in hematologic malignancies and post-HSCT relapses.
Keyphrases
- induced apoptosis
- end stage renal disease
- cell cycle arrest
- clinical trial
- ejection fraction
- chronic kidney disease
- newly diagnosed
- hematopoietic stem cell
- peritoneal dialysis
- prognostic factors
- acute myeloid leukemia
- type diabetes
- randomized controlled trial
- endoplasmic reticulum stress
- oxidative stress
- signaling pathway
- cell death
- palliative care
- study protocol
- patient reported outcomes
- pi k akt