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. 2019 Aug 29;20(17):4233. doi: 10.3390/ijms20174233

Table 6.

Mechanisms of resistance of leukemic stem cells (LSC) against immunotherapies.

Mechanism Possible Strategy to Overcome Resistance
Intrinsic resistance Antibody-based targeting of LSC
LSC quiescence Antibody-based targeting of LSC
Priming LSC into the cell cycle
Expression of MDR MDR-targeting drugs or CAR cells
Loss of cell surface targets Mixtures of antibodies or CAR cells directed against two or more surface targets, drug combinations, or
combination of drug therapy with HSCT
Immune checkpoint-induced LSC resistance Checkpoint-targeting antibodies
Checkpoint-targeting CAR cells
BET/MYC-targeting drugs *
JAK/STAT-targeting drugs
BM niche-related resistance Niche cell-targeting drugs
Osteoblastic niche BET/MYC-targeting drugs *
Vascular niche Specific anti-angiogenic drugs
LSC retention in niche Mobilizing drugs (plerixafor)
LSC hypermobilization Mobilization blocker (e.g., gliptins)
General immunosuppression Repeated T/NK cell infusion
Blocked immune cells Bispecific antibodies against LSC and immune effector cells
Loss of CAR-T cells or
CAR-NK cells
Repeated infusions of CAR cells
Development of blocking antibodies against CARs Use of single domain scFvs
Humanize the scFvs

* BET/MYC-targeting drugs can suppress cytokine-induced and oncogene-induced expression of PD-L1 on LSC in AML and CML as well as osteoblast-induced resistance. Abbreviations: LSC, leukemic stem cells; MDR, multi-drug resistance gene product; HSCT, hematopoietic stem cell transplantation; CAR, chimeric antigen receptor; NK cells; natural killer cells; scFvs, single chain variable fragments.