Research Article: Production of functional CD19 CAR T cells under hypoxic manufacturing conditions
Abstract:
Chronic lymphocytic leukemia (CLL) has proven difficult to treat with chimeric antigen receptor (CAR) T cell therapy. CLL cells can negatively alter T cell fitness and induce a pseudohypoxic state. We hypothesized that production of CAR T cells under restricted oxygen conditions resembling physiological oxygen levels that can be encountered in tissues ( i.e. 2% O 2 ) could promote outgrowth of hypoxia-tolerant CAR T cells.
We performed in vitro phenotypic and functional assessments of CD19-directed CAR T cells produced in either 21% ( Nor CAR) or 2% ( Hyp CAR) O 2 derived from healthy donors (HDs) or patients with CLL.
Production of HD-derived CAR T cells in 2% O 2 promoted the enrichment of a naïve-like subset. Hyp CAR and Nor CAR cells were functionally distinct; CD4+ Hyp CAR cells produced more IL-2 and tumor necrosis factor than CD4+ Nor CAR cells. Production in 2% O 2 was not detrimental to viability or proliferation upon cognate antigen-stimulation and led to increased activation. After chronic stimulation in hypoxia, Hyp CAR-product remained enriched in naïve-like cells, and demonstrated cytotoxic and cytokine production capacity. In CAR T cells derived from patients with CLL, Nor CAR and Hyp CAR subsets were functionally and phenotypically comparable, but displayed different mitochondrial metabolism.
We demonstrated that production in 2% O 2 is not detrimental, confers subtle but lasting functional and phenotypic changes in CAR T cells warranting further research on the impact of hypoxic production on CAR T cell functionality in hypoxic tumor microenvironments.
Introduction:
Chronic lymphocytic leukemia (CLL) has proven difficult to treat with chimeric antigen receptor (CAR) T cell therapy. CLL cells can negatively alter T cell fitness and induce a pseudohypoxic state. We hypothesized that production of CAR T cells under restricted oxygen conditions resembling physiological oxygen levels that can be encountered in tissues ( i.e. 2% O 2 ) could promote outgrowth of hypoxia-tolerant CAR T cells.
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